69 results on '"Hashemi D"'
Search Results
2. LB973 Cutaneous surgical wounds have distinct microbiomes from intact skin
- Author
-
Gupta, S., primary, Poret, A.J., additional, Hashemi, D., additional, Esenou, A., additional, Yu, S.H., additional, D'Gama, J., additional, Neel, V.A., additional, and Lieberman, T.D., additional
- Published
- 2022
- Full Text
- View/download PDF
3. AMPK signaling in diabetes mellitus, insulin resistance and diabetic complications: A pre-clinical and clinical investigation
- Author
-
Entezari, M., Hashemi, D., Taheriazam, A., Zabolian, A., Fakhri, F., Hashemi, M., Hushmandi, K., Ashrafizadeh, M., Zarrabi, A., Ertas, Y.N., Mirzaei, S., İstinye Üniversitesi, Mühendislik ve Doğa Bilimleri Fakültesi, Biyomedikal Mühendisliği Bölümü, and Zarrabi, Ali
- Subjects
Glucose metabolism ,Insulin resistance ,Diabetic complication ,Diabetic patients ,Clinical application - Abstract
Diabetes mellitus (DM) is considered as a main challenge in both developing and developed countries, as lifestyle has changed and its management seems to be vital. Type I and type II diabetes are the main kinds and they result in hyperglycemia in patients and related complications. The gene expression alteration can lead to development of DM and related complications. The AMP-activated protein kinase (AMPK) is an energy sensor with aberrant expression in various diseases including cancer, cardiovascular diseases and DM. The present review focuses on understanding AMPK role in DM. Inducing AMPK signaling promotes glucose in DM that is of importance for ameliorating hyperglycemia. Further investigation reveals the role of AMPK signaling in enhancing insulin sensitivity for treatment of diabetic patients. Furthermore, AMPK upregulation inhibits stress and cell death in β cells that is of importance for preventing type I diabetes development. The clinical studies on diabetic patients have shown the role of AMPK signaling in improving diabetic complications such as brain disorders. Furthermore, AMPK can improve neuropathy, nephropathy, liver diseases and reproductive alterations occurring during DM. For exerting such protective impacts, AMPK signaling interacts with other molecular pathways such as PGC-1α, PI3K/Akt, NOX4 and NF-κB among others. Therefore, providing therapeutics based on AMPK targeting can be beneficial for amelioration of DM. 35062059
- Published
- 2022
4. Evidence for X(3872) in Pb-Pb Collisions and Studies of its Prompt Production at root s(NN)=5.02 TeV
- Author
-
Sirunyan, A. M., Tumasyan, A., Adam, W., Ambrogi, F., Bergauer, T., Dragicevic, M., Ero, J., Del, Valle, Escalante, A., Flechl, M., Fruhwirth, R., Jeitler, M., Krammer, N., Kratschmer, I, Liko, D., Madlener, T., Mikulec, I, Rad, N., Schieck, J., Schofbeck, R., Spanring, M., Waltenberger, W., Wulz, C-E, Zarucki, M., Drugakov, V, Mossolov, V, Gonzalez, Suarez, J., Darwish, M. R., Wolf, De, E. A., Croce, Di, Janssen, D., Kello, X., Lelek, T., Pieters, A., Sfar, M., Rejeb, H., Van, Haevermaet, Van, Mechelen, Van, Putte, Van, Remortel, Blekman, N., Bols, F., Chhibra, E. S., D'Hondt, S. S., Clercq, De, Lontkovskyi, J., Lowette, D., Marchesini, S., Moortgat, I, Python, S., Tavernier, Q., Van, Doninck, Van, Mulders, Beghin, P., Bilin, D., Clerbaux, B., Lentdecker, De, Delannoy, G., Dorney, H., Favart, B., Grebenyuk, L., Kalsi, A., Moureaux, A. K., Popov, L., Postiau, A., Starling, N., Thomas, E., L. V., Velde, Er, Vanlaer, C., Vannerom, P., Cornelis, D., Dobur, T., Khvastunov, D., Niedziela, I, Roskas, M., Skovpen, C., Tytgat, K., Verbeke, M., Vermassen, W., Vit, B., Bruno, M., Caputo, G., David, C., Delaere, P., Delcourt, C., Giammanco, M., Lemaitre, A., Prisci, V, Aro, J., Saggio, A., Vischia, P., Zobec, J., Alves, G. A., Silva, Correia, G., Hensel, C., Moraes, A., Batista Das Chagas, Belchior, E., Carvalho, W., Chinellato, J., Coelho, E., Costa, Da, E. M., Silveira, Da, Damiao, G. G., De Jesus, D., Martins, De Oliveira, C., Souza, De, Fonseca, S., Malbouisson, H., Martins, J., Figueiredo, Matos, D., Jaime, Medina, M., Almeida, De, Melo, M., Herrera, Mora, C., Mundim, L., Nogima, H., Prado Da Silva, Teles, W. L., Rebello, P., Rosas, Sanchez, L. J., Santoro, A., Sznajder, A., Thiel, M., Tonelli, Manganote, E. J., Da Silva De Araujo, Torres, F., Pereira, Vilela, A., Bernardes, C. A., Calligaris, L., Fern, ez Perez Tomei, Gregores, T. R., Lemos, E. M., Mercadante, D. S., Novaes, P. G., Padula, S. F., S, Ra, S., Aleks, Rov, Antchev, A., Hadjiiska, G., Iaydjiev, R., Misheva, P., Rodozov, M., Shopova, M., Sultanov, M., Bonchev, G., Dimitrov, M., Ivanov, A., Litov, T., Pavlov, L., Petkov, B., Petrov, P., Fang, A., Gao, W., Yuan, X., Ahmad, L., Hu, M., Wang, Z., Chen, Y., Chen, G. M., Chen, H. S., Jiang, M., Leggat, C. H., Liao, D., Liu, H., Spiezia, Z., Tao, A., Yazgan, J., Zhang, E., Zhang, H., Zhao, S., Agapitos, J., Ban, A., Levin, G., Li, A., Li, J., Li, L., Mao, Q., Qian, Y., Wang, S. J., Wang, D., Xiao, Q., Avila, M., Cabrera, C., Florez, A., Gonzalez, Hern, C. F., Ez, Segura, Delgado, M. A., Mejia, Guisao, Ruiz, Alvarez, J. D., Salazar, Gonzalez, C. A., Vanegas, Arbelaez, Godinovic, N., Lelas, N., Puljak, D., Sculac, I, Antunovic, T., Kovac, Z., Brigljevic, M., Ferencek, V, Kadija, D., Mesic, K., Roguljic, B., Starodumov, M., Susa, A., Ather, T., Attikis, M. W., Erodotou, A., Ioannou, E., Kolosova, A., Konstantinou, M., Mavromanolakis, S., Mousa, G., Nicolaou, J., Ptochos, C., Razis, F., Rykaczewski, P. A., Saka, H., Tsiakkouri, H., Finger, D., Finger, M., r. M., J, Kveton, A., Tomsa, J., Ayala, E., Jarrin, Carrera, E., Mahmoud, M. A., Mohammed, Y., Bhowmik, S., Antunes De Oliveira, Carvalho, A., Dewanjee, R. K., Ehataht, K., Kadastik, M., Raidal, M., Veelken, C., Eerola, P., Forthomme, L., Kirschenmann, H., Osterberg, K., Voutilainen, M., Garcia, F., Havukainen, J., Heikkila, J. K., Karimaki, V, Kim, M. S., Kinnunen, R., Lampen, T., Lassila-Perini, K., Laurila, S., Lehti, S., Linden, T., Siikonen, H., Tuominen, E., Tuominiemi, J., Luukka, P., Tuuva, T., Besancon, M., Couderc, F., Dejardin, M., Denegri, D., Fabbro, B., Faure, J. L., Ferri, F., Ganjour, S., Givernaud, A., Gras, P., Monchenault, De, Hamel, G., Jarry, P., Leloup, C., Lenzi, B., Locci, E., Malcles, J., R, Er, Rosowsky, J., Sahin, A., Savoy-Navarro, M. O., Titov, A., Yu, M., Ahuja, G. B., Amendola, S., Beaudette, C., Bonanomi, F., Busson, M., Charlot, P., Diab, C., Falmagne, B., Cassagnac, De, Granier, R., Kucher, I, Lobanov, A., Perez, Martin, C., Nguyen, M., Och, O, Paganini, C., Rembser, P., Salerno, J., Sauvan, R., Sirois, J. B., Zabi, Y., Zghiche, A., Agram, A., J-L, Rea, Bloch, J., Bourgatte, D., Brom, G., J-M, Chabert, Collard, E. C., Conte, C., Fontaine, E., J-C, Gele, Goerlach, D., Grimault, U., Bihan, Le, A-C, Tonon, Van, Hove, Gadrat, P., Beauceron, S., Bernet, S., Boudoul, C., Camen, G., Carle, C., Chanon, A., Chierici, N., Contardo, R., Depasse, D., Mamouni, El, Fay, H., Gascon, J., Gouzevitch, S., Ille, M., Jain, B., Laktineh, Sa, Lattaud, I. B., Lesauvage, H., Lethuillier, A., Mirabito, M., Perries, L., Sordini, S., Torterotot, V, Touquet, L., G. V., Donckt, Er, Viret, M., Toriashvili, S., Tsamalaidze, T., Autermann, Z., Feld, C., Klein, L., Lipinski, K., Meuser, M., Pauls, D., Preuten, A., Rauch, M., Schulz, M. P., Teroerde, J., Erdmann, M., Fischer, M., Ghosh, B., Hebbeker, S., Hoepfner, T., Keller, K., Mastrolorenzo, H., Merschmeyer, L., Meyer, M., Millet, A., Mocellin, P., Mondal, G., Mukherjee, S., Noll, S., Novak, D., Pook, A., Pozdnyakov, T., Quast, A., Radziej, T., Rath, M., Reithler, Y., Roemer, H., Schmidt, J., Schuler, A., Sharma, S. C., Wiedenbeck, A., Zaleski, S., Flugge, S., Ahmad, G., Haj, W., Hlushchenko, O., Kress, T., Muller, T., Nowack, A., Pistone, C., Pooth, O., Roy, D., Sert, H., Stahl, A., Martin, Aldaya, M., Asmuss, P., Babounikau, I, Bakhshiansohi, H., Beernaert, K., Behnke, O., Martinez, Bermudez, A., Bin, Anuar, Borras, A. A., Botta, K., Campbell, V, Cardini, A., Connor, A., Rodriguez, P., Consuegra, S., Contreras-Campana, C., Danilov, V, Wit, De, Defranchis, A., Pardos, M. M., Diez, C., Damiani, Dominguez, D., Eckerlin, G., Eckstein, D., Eichhorn, T., Elwood, A., Eren, E., Banos, Estevez, L. I., Gallo, E., Geiser, A., Grohsjean, A., Guthoff, M., Haranko, M., Harb, A., Jafari, A., Jomhari, N. Z., Jung, H., Kasem, A., Kasemann, M., Kaveh, H., Keaveney, J., Kleinwort, C., Knolle, J., Krucker, D., Lange, W., Lenz, T., Lidrych, J., Lipka, K., Lohmann, W., Mankel, R., Melzer-Pellmann, I-A, Meyer, A. B., Missiroli, M., Mnich, J., Mussgiller, A., Myronenko, V, Adan, Perez, D., Pflitsch, S. K., Pitzl, D., Raspereza, A., Saibel, A., Savitskyi, M., Scheurer, V, Schutze, P., Schwanenberger, C., Shevchenko, R., Singh, A., Ricardo, Sosa, R. E., Tholen, H., Turkot, O., Vagnerini, A., Van De Klundert, Walsh, M., Wen, R., Wichmann, Y., Wissing, K., Zenaiev, C., Zlebcik, O., Aggleton, R., Bein, R., Benato, S., Benecke, L., Dreyer, A., Ebrahimi, T., Feindt, A., Frohlich, F., Garbers, A., Garutti, C., Gonzalez, E., Gunnellini, D., Haller, P., Hinzmann, J., Karavdina, A., Kasieczka, A., Klanner, G., Kogler, R., Kovalchuk, R., Kurz, N., Kutzner, S., Lange, V, Lange, J., Malara, T., Multhaup, A., Niemeyer, J., Reimers, C. E. N., Rieger, A., Schleper, O., Schumann, P., Schw, S., T, J., Sonneveld, J., Stadie, H., Steinbruck, G., Vormwald, B., Zoi, I, Akbiyik, M., Baselga, M., Baur, S., Berger, T., Butz, E., Caspart, R., Chwalek, T., Boer, De, Dierlamm, W., Morabit, El, Faltermann, K., Giffels, N., Gottmann, M., Hartmann, A., Heidecker, F., Husemann, C., Iqbal, U., Kudella, M. A., Maier, S., Mitra, S., Mozer, S., Muller, M. U., Muller, D., Musich, Th, Nurnberg, M., Rabbertz, G., Savoiu, K., Schafer, D., Schnepf, D., Schroder, M., Shvetsov, M., Simonis, I, Ulrich, H. J., Wassmer, R., Weber, M., Wohrmann, M., Wolf, C., Wozniewski, R., Anagnostou, S., Asenov, G., Daskalakis, P., Geralis, G., Kyriakis, T., Loukas, A., Paspalaki, D., Stakia, G., Diamantopoulou, A., Karathanasis, M., Kontaxakis, G., Manousakis-katsikakis, P., Panagiotou, A., Papavergou, A., Saoulidou, I, Theofilatos, N., Vellidis, K., Vourliotis, K., Bakas, E., Kousouris, G., Papakrivopoulos, K., Tsipolitis, I, Zacharopoulou, G., Evangelou, A., Foudas, I, Gianneios, C., Katsoulis, P., Kokkas, P., Mallios, P., Manitara, S., Manthos, K., Papadopoulos, N., Strologas, I, Triantis, J., Tsitsonis, F. A., Bartok, D., Chudasama, M., Csanad, R., Major, M., P. M., Al, K., Mehta, A., Pasztor, G., Suranyi, O., Veres, I, Bencze, G., Hajdu, G., Horvath, C., Sikler, D., Veszpremi, F., Vesztergombi, V., Beni, G., Czellar, N., Karancsi, S., Molnar, J., Szillasi, J., Raics, Z., Teyssier, P., Trocsanyi, D., Ujvari, Z. L., Csorgo, B., Metzger, T., Nemes, W. J., Novak, F., Choudhury, T., Komaragiri, S., Tiwari, J. R., Bahinipati, P. C., Kar, S., Kole, C., Mal, G., Bindhu, P., Muraleedharan Nair, V. K., Nayak, A., Sahoo, D. K., Swain, S. K., Bansal, S., Beri, S. B., Bhatnagar, V, Chauhan, S., Dhingra, N., Gupta, R., Kaur, A., Kaur, M., Kaur, S., Kumari, P., Lohan, M., Meena, M., Eep, S, Sharma, K., Singh, S., Virdi, J. B., Walia, A. K., Bhardwaj, G., Choudhary, A., Garg, B. C., Gola, R. B., Keshri, M., Kumar, S., Ashok, Naimuddin, Priyanka, M., Ranjan, P., Shah, K., Aashaq, Sharma, Bhardwaj, R., Bharti, R., Bhattacharya, M., Bhattacharya, R., Bhaw, S., Eep, U., Bhowmik, D., Dutta, S., Ghosh, S., Gomber, B., Maity, M., Mondal, K., N, An, Purohit, S., Rout, A., Saha, P. K., Sarkar, G., Sharan, S., Singh, M., Thakur, B., Behera, S., Behera, P. K., Kalbhor, S. C., Muhammad, P., Pujahari, A., Sharma, P. R., Sikdar, A., Dutta, A. K., Jha, D., Mishra, V, Netrakanti, D. K., Pant, P. K., Shukla, L. M., Aziz, P., Bhat, T., Dugad, M. A., Mohanty, S., Sur, G. B., Verma, N., Ravindra, Kumar, Banerjee, S., Bhattacharya, S., Chatterjee, S., Das, P., Guchait, M., Karmakar, S., Majumder, G., Mazumdar, K., Sahoo, N., Sawant, S., Dube, S., Kansal, B., Kapoor, A., Kothekar, K., P, Ey, Rane, S., Rastogi, A., Sharma, A., Chenarani, S., Etesami, S., Khakzad, S. M., Najafabadi, M., Mohammadi, M., Naseri, M., Hosseinabadi, Rezaei, F., Felcini, M., Grunewald, M., Abbrescia, M., Aly, R., Calabria, C., Colaleo, A., Creanza, D., Cristella, L., Filippis, De, Palma, De, Florio, Di, Elmetenawee, A., Fiore, W., Gelmi, L., Iaselli, A., Ince, G., Lezki, M., Maggi, S., Maggi, G., Merlin, M., Miniello, J. A., My, G., Nuzzo, S., Pompili, S., Pugliese, A., Radogna, G., Ranieri, R., Selvaggi, A., Silvestris, G., Simone, L., Venditti, F. M., Verwilligen, R., Abbiendi, P., Battilana, G., Bonacorsi, C., Borgonovi, D., Braibant-Giacomelli, L., Campanini, S., Capiluppi, R., Castro, P., Cavallo, A., Codispoti, F. R., Cuffiani, G., Dallavalle, M., Fabbri, G. M., Fanfani, F., Fontanesi, A., Giacomelli, E., Giommi, P., Gr, L., I, C., Guiducci, L., Iemmi, F., Meo, Lo, Marcellini, S., Masetti, S., Navarria, G., Perrotta, F. L., Primavera, A., Rossi, F., Rovelli, A. M., Siroli, T., Tosi, G. P., Albergo, N., Costa, S., Mattia, Di, Potenza, A., Tricomi, R., Tuve, A., Barbagli, C., Cassese, G., Ceccarelli, A., Ciulli, R., Civinini, V, D'Aless, C., Ro, R., Fiori, F., Focardi, E., Latino, G., Lenzi, P., Meschini, M., Paoletti, S., Sguazzoni, G., Viliani, L., Benussi, L., Bianco, S., Piccolo, D., Bozzo, M., Ferro, F., Mulargia, R., Robutti, E., Tosi, S., Benaglia, A., Beschi, A., Brivio, F., Ciriolo, V, Dinardo, M. E., Dini, P., Gennai, S., Ghezzi, A., Govoni, P., Guzzi, L., Malberti, M., Malvezzi, S., Menasce, D., Monti, F., Moroni, L., Paganoni, M., Pedrini, D., Ragazzi, S., Fatis, De, Tabarelli, T., Valsecchi, D., Zuolo, D., Buontempo, S., Cavallo, N., Iorio, De, Crescenzo, Di, Fabozzi, A., Fienga, F., Galati, F., Iorio, G., Layer, A. O. M., Lista, L., Meola, L., Paolucci, S., Rossi, P., Sciacca, B., Voevodina, C., Azzi, E., Bacchetta, P., Bisello, N., Boletti, D., Bragagnolo, A., Carlin, A., Checchia, R., Manzano, P., De Castro, P., Dorigo, T., Dosselli, U., Gasparini, F., Gasparini, U., Gozzelino, A., Hoh, S. Y., Margoni, M., Meneguzzo, A. T., Pazzini, J., Presilla, M., Ronchese, P., Rossin, R., Simonetto, F., Tiko, A., Tosi, M., Zanetti, M., Zotto, P., Zucchetta, A., Zumerle, G., Braghieri, A., Fiorina, D., Montagna, P., Ratti, S. P., Re, V, Ressegotti, M., Riccardi, C., Salvini, P., Vai, I, Vitulo, P., Biasini, M., Bilei, G. M., Ciangottini, D., Fano, L., Lariccia, P., Leonardi, R., Manoni, E., Mantovani, G., Mariani, V, Menichelli, M., Rossi, A., Santocchia, A., Spiga, D., Rosov, K., Azzurri, P., Bagliesi, G., Bertacchi, V, Bianchini, L., Boccali, T., Castaldi, R., Ciocci, M. A., Dell'Orso, R., Donato, S., Giannini, L., Giassi, A., Grippo, M. T., Ligabue, F., Manca, E., Orli, M, Messineo, G., Palla, A., Rizzi, F., Rol, A., I, G., Chowdhury, Roy, S., Scribano, A., Spagnolo, P., Tenchini, R., Tonelli, G., Turini, N., Venturi, A., Verdini, P. G., Cavallari, F., Cipriani, M., Del, Re, Marco, Di, Diemoz, E., Longo, M., Meridiani, E., Organtini, P., G. P., Olfi, F., Paramatti, R., Quaranta, C., Rahatlou, S., Rovelli, C., Santanastasio, F., Soffi, L., Tramontano, R., Amapane, N., Arcidiacono, R., Argiro, S., Arneodo, M., Bartosik, N., Bellan, R., Bellora, A., Biino, C., Cappati, A., Cartiglia, N., Cometti, S., Costa, M., Covarelli, R., Demaria, N., Fern, Ez, Gonzalez, J. R., Kiani, B., Legger, F., Mariotti, C., Maselli, S., Migliore, E., Monaco, V, Monteil, E., Monteno, M., Obertino, M. M., Ortona, G., Pacher, L., Pastrone, N., Pelliccioni, M., Angioni, Pinna, G. L., Romero, A., Ruspa, M., Salvatico, R., Sola, V, Solano, A., Soldi, D., Staiano, A., Trocino, D., Belforte, S., Elise, C, Casarsa, V, Cossutti, M., Rold, Da, Della, Ricca, Vazzoler, G., Zanetti, F., Kim, A., Kim, B., Kim, D. H., Lee, G. N., Lee, J., Moon, S. W., C. S., Oh, Pak, Y. D., I, S., Sekmen, S., Son, D. C., Yang, Y. C., Kim, H., Moon, D. H., Francois, B., Kim, T. J., Park, J., Cho, S., Choi, S., Go, Y., Ha, S., Hong, B., Lee, K., Lee, K. S., Lim, J., Park, S. K., Roh, Y., Yoo, J., Goh, J., Kim, H. S., Almond, J., Bhyun, J. H., Choi, J., Jeon, S., Kim, J., Kim, J. S., Lee, H., Lee, S., Nam, K., Oh, M., S. B., Oh, Radburn-Smith, B. C., Yang, U. K., Yoo, H. D., Yoon, I, Jeon, D., Kim, J. H., Lee, J. S. H., Park, I. C., Watson, I. J., Choi, Y., Hwang, C., Jeong, Y., Lee, Y., Yu, I, Veckalns, V., Dudenas, V, Juodagalvis, A., Rinkevicius, A., Tamulaitis, G., Vaitkus, J., Idris, Mohamad, F., Abdullah, Wan, W. A. T., Yusli, M. N., Zolkapli, Z., Benitez, J. F., Hern, Ez, Castaneda, A., Quijada, Murillo, J. A., Palomo, Valencia, L., Castilla-Valdez, H., De La Cruz-Burelo, Heredia-De La Cruz, Lopez-Fern, I, Ez, R., Sanchez-Hern, Ez, Moreno, A., Carrillo, S., Oropeza, Barrera, Ramirez-Garcia, C., Vazquez, Valencia, Eysermans, F., Pedraza, J., I, Salazar, Ibarguen, H. A., Uribe, Estrada, Pineda, C., Morelos, A., Mijuskovic, J., Raicevic, N., Krofcheck, D., Bheesette, S., Butler, P. H., Lujan, P., Ahmad, A., Ahmad, M., Awan, M. I. M., Hassan, Q., Hoorani, H. R., Khan, W. A., Shah, M. A., Shoaib, M., Waqas, M., Avati, V, Grzanka, L., Malawski, M., Bialkowska, H., Bluj, M., Boimska, B., Gorski, M., Kazana, M., Szleper, M., Zalewski, P., Bunkowski, K., Byszuk, A., Doroba, K., Kalinowski, A., Konecki, M., Krolikowski, J., Olszewski, M., Walczak, M., Araujo, M., Bargassa, P., Bastos, D., Francesco, Di, Faccioli, A., Galinhas, P., Gallinaro, B., Hollar, M., Leonardo, J., Niknejad, N., Seixas, T., Shchelina, J., Strong, K., Toldaiev, G., Varela, O., Afanasiev, J., Bunin, S., Ershov, P., Golutvin, Y., Gorbunov, I, Kamenev, I, Karjavine, A., Korenkov, V, Lanev, V, Malakhov, A., Matveev, A., Mitsyn, V, Moisenz, V. V., Palichik, P., Perelygin, V, Shmatov, V, Skatchkov, S., Yuldashev, N., Zarubin, B. S., Zhiltsov, A., Chtchipounov, V, Golovtcov, L., Ivanov, V, Kim, Y., Kuznetsova, V, Levchenko, E., Murzin, P., Oreshkin, V, Smirnov, V, Sosnov, I, Sulimov, D., Uvarov, V, Vorobyev, L., Reev, A., Dermenev, Yu, Gninenko, A., Golubev, S., Karneyeu, N., Kirsanov, A., Krasnikov, M., Pashenkov, N., Tlisov, A., Toropin, D., Epshteyn, A., Gavrilov, V, Lychkovskaya, V, Nikitenko, N., Popov, A., Pozdnyakov, V, Safronov, I, Spiridonov, G., Stepennov, A., Toms, A., Vlasov, M., Zhokin, E., Aushev, A., Bychkova, T., Chistov, O., Danilov, R., Polikarpov, M., Tarkovskii, S., Reev, E., Azarkin, V, Dremin, M., Kirakosyan, I, Terkulov, M., Belyaev, A., Boos, A., Demiyanov, E., Ershov, A., Gribushin, A., Kodolova, A., Korotkikh, O., Lokhtin, V, Obraztsov, I, Petrushanko, S., Savrin, S., Snigirev, V, Vardanyan, A., Barnyakov, I, Blinov, A., Dimova, V, Kardapoltsev, T., Skovpen, L., Azhgirey, Y., Bayshev, I, Bitioukov, I, Kachanov, S., Konstantinov, V, D. M., Rik, P., Petrov, V, Ryutin, R., Slabospitskii, S., Sobol, A., Troshin, S., Tyurin, N., Uzunian, A., Volkov, A., Babaev, A., Iuzhakov, A., Okhotnikov, V, Borchsh, V, Ivanchenko, V, Tcherniaev, E., Adzic, P., Cirkovic, P., Dordevic, M., Milenovic, P., Milosevic, J., Stojanovic, M., Aguilar-Benitez, M., Alcaraz, Maestre, Alvarez, Fern, Ez, A., Bachiller, I, Barrio, Luna, Bedoya, M., Cristina, F., Brochero, Cifuentes, J. A., Carrillo, Montoya, Cepeda, C. A., Cerrada, M., Colino, M., De la Cruz, Delgado, Peris, Fern, A., Ramos, Ez, Flix, J. P., Fouz, J., M. C., Gonzalez, Lopez, Goy, Lopez, Hern, S., J. M., Ez, Josa, I, Moran, M., Navarro, Tobar, Perez-Calero, Yzquierdo, Puerta, Pelayo, Redondo, J., Romero, I, Sanchez, Navas, Soares, S., Triossi, M. S., Willmott, A., Albajar, C., Troconiz, De, Reyes-Almanza, J. F., Alvarez, Gonzalez, Cuevas, B., Erice, J., Fern, C., Menendez, Ez, Folgueras, J., Gonzalez, Caballero, Palencia, Cortezon, Ramon, Alvarez, Rodriguez, Bouza, V, Sanchez, Cruz, Cabrillo, S., Calderon, I. J., Chazin, Quero, Duarte, Campderros, Fern, J., Ez, M., Manteca, Ez, P. J., Garcia, Alonso, Gomez, A., Martinez, Rivero, Martinez Ruiz del Arbol, Matorras, P., Piedra, Gomez, Prieels, J., Ricci-Tam, C., Rodrigo, F., Ruiz-Jimeno, T., Russo, A., Scodellaro, L., Vila, L., Vizan, Garcia, Sonnadara, J. M., Dharmaratna, D. U. J., Wickramage, W. G. D., Aarrestad, N., Abbaneo, T. K., Akgun, D., Auffray, B., Auzinger, E., Baechler, G., Baillon, J., Ball, P., Barney, A. H., Bendavid, D., Bianco, J., Bocci, M., Bortignon, A., Bossini, P., Brondolin, E., Camporesi, E., Caratelli, T., Cerminara, A., Chapon, G., Cucciati, E., D'Enterria, G., Dabrowski, D., Daci, A., Daponte, N., David, V, Davignon, A., Roeck, De, Deile, A., Maria, Di, Dobson, R., Dunser, M., Dupont, M., Elliott-Peisert, N., Emriskova, A., Fallavollita, N., Fasanella, F., Fiorendi, D., Franzoni, S., Fulcher, G., Funk, J., Giani, W., Gigi, S., Gill, D., Glege, K., Gouskos, F., Gruchala, L., Guilbaud, M., Gulhan, M., Hegeman, D., Heidegger, J., Iiyama, C., Innocente, Y., James, V, Janot, T., Karacheban, P., Kaspar, O., Kieseler, J., Krammer, J., Kratochwil, M., Lange, N., Lecoq, C., Long, P., Lourenco, K., Malgeri, C., Mannelli, L., Massironi, M., Meijers, A., Mersi, F., Meschi, S., Moortgat, E., Mulders, F., Ngadiuba, M., Niedziela, J., Nourbakhsh, J., Orfanelli, S., Orsini, S., Pantaleo, L., Pape, F., Perez, L., Peruzzi, E., Petrilli, M., Petrucciani, A., Pfeiffer, G., Pierini, A., Pitters, M., Rabady, F. M., Racz, D., Rovere, M., Sakulin, M., Salfeld-Nebgen, H., Scarfi, J., Schafer, S., Schwick, C., Selvaggi, C., Sharma, M., Silva, A., Snoeys, P., Sphicas, W., Steggemann, P., Summers, J., Tavolaro, S., Treille, V. R., Tsirou, D., Van, Onsem, Vartak, G. P., Verzetti, A., Wozniak, M., Zeuner, K. A., Caminada, W. D., Deiters, L., Erdmann, K., Horisberger, W., Ingram, R., Kaestli, Q., Kotlinski, H. C., Langenegger, D., Rohe, U., Backhaus, T., Berger, M., Cal, P., Ri, A., Chernyavskaya, N., Dissertori, G., Dittmar, M., Donega, M., Dorfer, C., Espinosa, Gomez, T. A., Grab, C., Hits, D., Lustermann, W., Manzoni, R. A., Meinhard, M. T., Micheli, F., Musella, P., Nessi-Tedaldi, F., Pauss, F., Perovic, V, Perrin, G., Perrozzi, L., Pigazzini, S., Ratti, M. G., Reichmann, M., Reissel, C., Reitenspiess, T., Ristic, B., Ruini, D., Becerra, Sanz, D. A., Schonenberger, M., Shchutska, L., Olsson, Vesterbacka, M. L., Wallny, R., Zhu, D. H., Amsler, C., Botta, C., Brzhechko, D., Canelli, M. F., Cosa, De, Del, Burgo, Kilminster, R., Leontsinis, B., Mikuni, S., Neutelings, V. M., Rauco, I, Robmann, G., Schweiger, P., Takahashi, K., Wertz, Y., Kuo, S., Lin, C. M., Roy, W., Sarkar, A., Yu, T., Chang, S. S., Chao, P., Chen, K. F., Hou, P. H., W-S, Li, Y. Y., Lu, R-S, Paganis, Psallidas, E., Steen, A., Asavapibhop, A., Asawatangtrakuldee, B., Srimanobhas, C., Suwonj, N., Ee, N., Bat, A., Boran, F., Celik, A., Damarseckin, S., Demiroglu, Z. S., Dolek, F., Dozen, C., Dumanoglu, I, Gokbulut, G., Guler, Emine, Gurpinar, Guler, Y., Hos, I, Isik, C., Kangal, E. E., Kara, O., Topaksu, Kayis, A., Kiminsu, U., Onengut, G., Ozdemir, K., Simsek, A. E., Tok, U. G., Turkcapar, S., Zorbakir, I. S., Zorbilmez, C., Isildak, B., Karapinar, G., Yalvac, M., Atakisi, I. O., Gulmez, E., Kaya, M., Kaya, O., Tekten, S., Yetkin, E. A., Cakir, A., Cankocak, K., Komurcu, Y., Sen, S., Cerci, S., Kaynak, B., Ozkorucuklu, S., Cerci, Sunar, D., Grynyov, B., Levchuk, L., Bhal, E., Bologna, S., Brooke, J. J., Burns, D., Clement, E., Cussans, D., Flacher, H., Goldstein, J., Heath, G. P., Heath, H. F., Kreczko, L., Krikler, B., Paramesvaran, S., Sakuma, T., Nasr-Storey, El, Seif, S., Smith, V. J., Taylor, J., Titterton, A., Bell, K. W., Brew, C., Brown, R. M., Cockerill, D. J. A., Coughlan, J. A., Harder, K., Harper, S., Linacre, J., Manolopoulos, K., Newbold, D. M., Olaiya, E., Petyt, D., Reis, T., Schuh, T., Shepherd-Themistocleous, C. H., Thea, A., Tomalin, I. R., Williams, T., Bainbridge, R., Bloch, P., Bonomally, S., Borg, J., Breeze, S., Buchmuller, O., Bundock, A., Chahal, Gurpreet, Singh, Colling, D., Dauncey, P., Davies, G., Della, Negra, Everaerts, M., Hall, P., Iles, G., Komm, G., Langford, M., Lyons, J., Magnan, L., A-M, Malik, Martelli, S., Milosevic, A., Morton, V, Nash, A., Palladino, J., Pesaresi, V, Raymond, M., Richards, D. M., Rose, A., Scott, A., Seez, E., Shtipliyski, C., Stoye, A., Strebler, M., Tapper, T., Uchida, A., Virdee, K., Wardle, T., Webb, N., Winterbottom, S. N., Zecchinelli, D., Zenz, A. G., Cole, S. C., Hobson, J. E., Khan, P. R., Kyberd, A., Mackay, P., Reid, C. K., Teodorescu, I. D., Zahid, L., Brinkerhoff, S., Call, A., Caraway, K., Dittmann, B., Hatakeyama, J., Madrid, K., Mcmaster, C., Pastika, B., Smith, N., Bartek, C., Dominguez, R., Uniyal, A., Hern, R., Vargas, A. M., Buccilli, A., Cooper, I, Gleyzer, S., V, S., Henderson, C., Rumerio, P., West, C., Albert, A., Arcaro, D., Demiragli, Z., Gastler, D., Richardson, C., Rohlf, J., Sperka, D., Spitzbart, D., Suarez, I, Sulak, L., Zou, D., Benelli, G., Burkle, B., Coubez, X., Cutts, D., Duh, Y. T., Hadley, M., Heintz, U., Hogan, J. M., Kwok, K. H. M., Laird, E., Sberg, L, Lau, G., Lee, K. T., Narain, J., Sagir, M., Syarif, S., Usai, R., Wong, E., W. Y., Yu, Zhang, D., W. B., Brainerd, R., Breedon, C., Sanchez, R., Calderon De La Barca, M., Chertok, M., Conway, J., Conway, R., Cox, P. T., Erbacher, R., Flores, C., Funk, G., Jensen, F., Ko, W., Kukral, O., L, Er, Mulhearn, R., Pellett, M., Pilot, D., Shi, J., Taylor, M., Tos, D., Tripathi, K., Wang, M., Zhang, Z., Bachtis, F., Bravo, M., Cousins, C., Dasgupta, R., Florent, A., Hauser, A., Ignatenko, J., Mccoll, M., Nash, N., Regnard, W. A., Saltzberg, S., Schnaible, D., Stone, C., Valuev, B., Burt, V., Chen, K., Clare, Y., Gary, R., Shirazi, J. W., Ghiasi, S. M. A., Hanson, G., Karapostoli, G., Long, O. R., Manganelli, N., Negrete, Olmedo, M., Paneva, I, Si, M., Wimpenny, W., Yates, S., Zhang, B. R., Branson, Y., Chang, J. G., Cittolin, P., Cooperstein, S., Deelen, S., Derdzinski, N., Duarte, M., Gerosa, J., Gilbert, R., Hashemi, D., Klein, B., Krutelyov, D., Letts, V, Masciovecchio, J., May, M., Padhi, S., Pieri, S., Tadel, V, Wurthwein, M., Yagil, F., Della, Porta, Zevi, G., Amin, N., Ari, Bh, Campagnari, R., Citron, C., Dutta, M., Inc, V, Ela, J., Marsh, B., Mei, H., Ovcharova, A., Qu, H., Richman, J., Sarica, U., Stuart, D., Wang, S., Erson, D., Bornheim, A., Cerri, O., Dutta, I, Lawhorn, J. M., Lu, N., Mao, J., Newman, H. B., Nguyen, T. Q., Pata, J., Spiropulu, M., Vlimant, J. R., Xie, S., Zhu, R. Y., Alison, J., Rews, M. B., Ferguson, T., Mudholkar, T., Paulini, M., Sun, M., Vorobiev, I, Weinberg, M., Cumalat, J. P., Ford, W. T., Macdonald, E., Mulholl, T., Patel, R., Perloff, A., Stenson, K., Ulmer, K. A., Wagner, S. R., Alex, Er, Cheng, J., Chu, Y., Datta, J., Frankenthal, A., Mcdermott, A., Patterson, K., Quach, J. R., Ryd, D., Tan, A., Tao, S. M., Thom, Z., Wittich, J., Zientek, P., Abdullin, M., Albrow, S., Alyari, M., Apollinari, M., Apresyan, G., Apyan, A., Banerjee, A., Bauerdick, S., Beretvas, L. A. T., Berry, A., Berryhill, D., Bhat, J., Burkett, P. C., Butler, K., Canepa, J. N., Cerati, A., Cheung, G. B., Chlebana, H. W. K., Cremonesi, F., Elvira, M., Freeman, V. D., Gecse, J., Gottschalk, Z., Gray, E., Green, L., Grunendahl, D., Gutsche, S., Hanlon, O., Harris, J., Hasegawa, R. M., Heller, S., Hirschauer, R., Jayatilaka, J., Jindariani, B., Johnson, S., Joshi, M., Klijnsma, U., Klima, T., Kortelainen, B., Kreis, M. J., Lammel, B., Lewis, S., Lincoln, J., Lipton, D., Liu, R., Liu, M., Lykken, T., Maeshima, J., Marraffino, K., Mason, J. M., Mcbride, D., Merkel, P., Mrenna, P., Nahn, S., O'Dell, S., Papadimitriou, V, Pedro, V, Pena, K., Ravera, C., Hall, F., Reinsvold, A., Ristori, L., Schneider, B., Sexton-Kennedy, E., Soha, A., Spalding, W. J., Spiegel, L., Stoynev, S., Strait, J., Taylor, L., Tkaczyk, S., Tran, V, Uplegger, N., Va, L., Ering, E. W., Vidal, R., Weber, H. A., Woodard, A., Acosta, D., Avery, P., Bourilkov, D., Cadamuro, L., Cherepanov, V, Errico, F., Field, R. D., Guerrero, D., Joshi, B. M., Kim, M., Konigsberg, J., Korytov, A., K. H., Lo, Matchev, K., Menendez, N., Mitselmakher, G., Rosenzweig, D., Shi, K., Wang, J., Zuo, X., Joshi, Y. R., Adams, T., Askew, A., Hagopian, S., Hagopian, V, Johnson, K. F., Khurana, R., Kolberg, T., Martinez, G., Perry, T., Prosper, H., Schiber, C., Yohay, R., Zhang, J., Baarm, M. M., Hohlmann, M., Noonan, D., Rahmani, M., Saunders, M., Yumiceva, F., Adams, M. R., Apanasevich, L., Betts, R. R., Cavanaugh, R., Chen, X., Dittmer, S., Evdokimov, O., Gerber, C. E., Hangal, D. A., Hofman, D. J., Kumar, V, Mills, C., Oh, G., Roy, T., Tonjes, M. B., Varelas, N., Viinikainen, J., Wang, H., Wang, X., Wu, Z., Alhusseini, M., Bilki, B., Dilsiz, K., Durgut, S., Rajula, G, Haytmyradov, R. P., Khristenko, M., Koseyan, V, Merlo, O. K., J-P, Mestvirishvili, Moeller, A., Nachtman, A., Ogul, J., Onel, H., Ozok, Y., Penzo, F., Snyder, A., Tiras, C., Wetzel, E., Yi, J., Blumenfeld, K., Cocoros, B., Eminizer, A., Gritsan, N., V, A., Hung, W. T., Kyriacou, S., Maksimovic, P., Mantilla, C., Roskes, J., Swartz, M., Vami, T. A., Barrera, Baldenegro, C., Baringer, P., Bean, A., Boren, S., Bylinkin, A., Isidori, T., Khalil, S., King, J., Krintiras, G., Kropivnitskaya, A., Lindsey, C., Majumder, D., Mcbrayer, W., Minafra, N., Murray, M., Rogan, C., Royon, C., Ers, S, Schmitz, S., Takaki, E., Tapia, J. D., Wang, Q., Williams, J., Wilson, G., Duric, S., Kaadze, K., Kim, D., Maravin, Y., Mendis, D. R., Mitchell, T., Modak, A., Mohammadi, A., Rebassoo, F., Wright, D., Baden, A., Baron, O., Belloni, A., Eno, S. C., Feng, Y., Hadley, N. J., Jabeen, S., Jeng, G. Y., Kellogg, R. G., Mignerey, A. C., Nabili, S., Seidel, M., Skuja, A., Tonwar, S. C., Wang, L., Wong, K., Abercrombie, D., Allen, B., Bi, R., Br, T, Busza, S., Cali, W., D'Alfonso, I. A., Ceballos, M., Gomez, G., Goncharov, M., Harris, P., Hsu, D., Klute, M., Kovalskyi, D., Lee, Y-J, Luckey, P. D., Maier, B., Marini, A. C., Mcginn, C., Mironov, C., Narayanan, S., Niu, X., Paus, C., Rankin, D., Rol, Rol, C., Shi, G., Stephans, Z., Sumorok, G. S. F., Tatar, K., Velicanu, K., Wyslouch, T. W., Chatterjee, B., Evans, R. M., Guts, A., Hansen, S., Hiltbr, P., Jain, J., Kubota, Sh, Lesko, Y., Mans, Z., Revering, J., Rusack, M., Saradhy, R., Schroeder, R., Strobbe, N., Wadud, N., Acosta, M. A., Oliveros, J. G., Bloom, S., Chauhan, K., Claes, S., Fangmeier, D. R., Finco, C., Golf, L., Kamalieddin, F., Kravchenko, R., Siado, I, Snow, J. E., Stieger, G. R., Tabb, B., Agarwal, W., Harrington, G., Iashvili, C., Kharchilava, I., Mclean, A., Nguyen, C., Parker, D., Pekkanen, A., Rappoccio, J., Roozbahani, S., Alverson, B., Barberis, G., Freer, E., Haddad, C., Hortiangtham, Y., Madigan, A., Marzocchi, G., Morse, B., Nguyen, D. M., Orimoto, V, Skinnari, T., Tishelman-Charny, L., Wamorkar, A., Wang, T., Wisecarver, B., Wood, A., Bhattacharya, D., Bueghly, S., Fedi, J., Gilbert, G., Gunter, A., Hahn, T., Odell, K. A., Schmitt, N., Sung, M. H., Velasco, K., Bucci, M., Dev, R., Goldouzian, N., Hildreth, R., Anampa, M., Hurtado, K., Jessop, C., Karmgard, D. J., Lannon, K., Li, W., Loukas, N., Marinelli, N., Mcalister, I, Meng, F., Musienko, Y., Ruchti, R., Siddireddy, P., Smith, G., Taroni, S., Wayne, M., Wightman, A., Wolf, M., Alimena, J., Bylsma, B., Cardwell, B., Durkin, L. S., Francis, B., Hill, C., Ji, W., Lefeld, A., Ling, T. Y., Winer, B. L., Dezoort, G., Elmer, P., Hardenbrook, J., Haubrich, N., Higginbotham, S., Kalogeropoulos, A., Kwan, S., Lange, D., Lucchini, M. T., Luo, J., Marlow, D., Mei, K., Ojalvo, I, Olsen, J., Palmer, C., Piroue, P., Stickl, D., Tully, C., Malik, S., Norberg, S., Barker, A., Barnes, V. E., Chawla, R., Das, S., Gutay, L., Jones, M., Jung, A. W., Mahakud, B., Miller, D. H., Negro, G., Neumeister, N., Peng, C. C., Piperov, S., Qiu, H., Schulte, J. F., Trevisani, N., Wang, F., Xiao, R., Xie, W., Cheng, T., Dolen, J., Parashar, N., Baty, A., Behrens, U., Dildick, S., Ecklund, K. M., Freed, S., Geurts, F. J. M., Kilpatrick, M., Kumar, Arun, Padley, B. P., Redjimi, R., Roberts, J., Rorie, J., Shi, W., Leiton, Stahl, A. G., Tu, Z., Zhang, A., Bodek, A., Barbaro, De, Demina, P., Dulemba, R., Fallon, J. L., Ferbel, C., Galanti, T., Garcia-Bellido, M., Hindrichs, A., Khukhunaishvili, O., Ranken, A., Taus, E., Chiarito, R., Chou, B., J. P. G., Rakota, A., Gershtein, Y., Halkiadakis, E., Hart, A., Heindl, M., Hughes, E., Kaplan, S., Laflotte, I, Lath, A., Montalvo, R., Nash, K., Osherson, M., Salur, S., Schnetzer, S., Somalwar, S., Stone, R., Thomas, S., Acharya, H., Delannoy, A. G., Spanier, S., Bouhali, O., Dalchenko, M., Mattia, De, Delgado, M., Eusebi, A., Gilmore, R., Huang, J., Kamon, T., Kim, T., Luo, H., Malhotra, S., Marley, S., Mueller, D., Overton, R., Pernie, D., Rathjens, L., Safonov, D., Akchurin, A., Damgov, N., Guio, De, Hegde, F., Kunori, V, Lamichhane, S., Mengke, S. W., Muthumuni, T., Peltola, S., Undleeb, T., Volobouev, S., Wang, I, Whitbeck, Z., Greene, A., Gurrola, S., Janjam, A., Johns, R., Maguire, W., Melo, C., Ni, A., Padeken, H., Romeo, K., Sheldon, F., Tuo, P., Velkovska, S., Verweij, J., Arenton, M., Barria, M. W., Cox, P., Cummings, B., Hakala, G., Hirosky, J., Joyce, R., Ledovskoy, M., Neu, A., Tannenwald, C., Wang, B., Wolfe, Y., Xia, E., Harr, F., Karchin, R., Poudyal, P. E., Sturdy, N., Thapa, J., Black, P., Bose, K., Buchanan, T., Caillol, J., Carlsmith, C., Dasu, D., Bruyn, De, Dodd, I, Galloni, L., He, C., Herndon, H., Herve, M., Hussain, A., Lanaro, U., Loeliger, A., Loveless, A., Sreekala, R., Madhusudanan, J., Mallampalli, A., Pinna, D., Ruggles, T., Savin, A., Sharma, V, Smith, W. H., Teague, D., Trembath-reichert, S., and Cms, Collaboration
- Subjects
MODEL ,Physics and Astronomy ,High Energy Physics::Experiment ,QUARK-GLUON PLASMA ,Nuclear Experiment - Abstract
The first evidence for X(3872) production in relativistic heavy ion collisions is reported. The X(3872) production is studied in lead-lead (Pb-Pb) collisions at a center-of-mass energy of root s(NN) = 5.02 TeV per nucleon pair, using the decay chain X(3872) -> J/psi pi(+)pi(-) -> mu(+) mu(-) pi(+)pi(-). The data were recorded with the CMS detector in 2018 and correspond to an integrated luminosity of 1.7 nb(-1). The measurement is performed in the rapidity and transverse momentum ranges vertical bar y vertical bar < 1.6 and 15 < p(T) < 50 GeV/c. The significance of the inclusive X(3872) signal is 4.2 standard deviations. The prompt X(3872) to psi 2S yield ratio is found to be rho(Pb-Pb) = 1.08 +/- 0.49(stat) +/- 0.52(syst), to be compared with typical values of 0.1 for pp collisions. This result provides a unique experimental input to theoretical models of the X(3872) production mechanism, and of the nature of this exotic state.
- Published
- 2022
5. Unconventional Conjugation via vinylMeSi(O−)2 Siloxane Bridges May Imbue Semiconducting Properties in [vinyl(Me)SiO(PhSiO1.5)8OSi(Me)vinyl-Ar] Double-Decker Copolymers
- Author
-
Guan, J., primary, Arias, J. J. R., additional, Tomobe, K., additional, Ansari, R., additional, Marques, M. de F. V., additional, Rebane, A., additional, Mahbub, S., additional, Furgal, J. C., additional, Yodsin, N., additional, Jungsuttiwong, S., additional, Hashemi, D., additional, Kieffer, J., additional, and Laine, R. M., additional
- Published
- 2020
- Full Text
- View/download PDF
6. Substrate-Controlled Magnetism: Fe Nanowires on Vicinal Cu Surfaces
- Author
-
Hashemi, D., primary, Waters, M. J., additional, Hergert, W., additional, Kieffer, J., additional, and Stepanyuk, V. S., additional
- Published
- 2020
- Full Text
- View/download PDF
7. Coronaviruses as the emerging threats for human health: should we be prepared for the future outbreaks of new coronaviruses?
- Author
-
Bahrami, R., primary, Hashemi, D., additional, Aziziraftar, S. Keshavarz, additional, and Rahimi, P., additional
- Published
- 2020
- Full Text
- View/download PDF
8. P5265Magnetic resonance multilayer assessment of strain in patients with heart failure
- Author
-
Tanacli, R, primary, Hashemi, D, additional, Lapinskas, T, additional, Duengen, H.-D, additional, Edelmann, F, additional, Gebker, R, additional, Pieske, B, additional, and Kelle, S, additional
- Published
- 2019
- Full Text
- View/download PDF
9. Unconventional Conjugation via vinylMeSi(O−)2 Siloxane Bridges May Imbue Semiconducting Properties in [vinyl(Me)SiO(PhSiO1.5)8 OSi(Me)vinyl-Ar] Double-Decker Copolymers.
- Author
-
Guan, J., Arias, J. J. R., Tomobe, K., Ansari, R., Marques, M. de F. V., Rebane, A., Mahbub, S., Furgal, J. C., Yodsin, N., Jungsuttiwong, S., Hashemi, D., Kieffer, J., and Laine, R. M.
- Published
- 2020
- Full Text
- View/download PDF
10. 4379Circulating miRNAs as a prognostic tool for heart failure related morbidity and mortality in patients suffering from stable HFpEF: a subgroup analysis of the ALDO-DHF trial
- Author
-
Petutschnigg, J, primary, De Ronde, M W J, additional, Trippel, T D, additional, Schleussner, L, additional, Baehr, F, additional, Hashemi, D, additional, Holzendorf, V, additional, Leenders, J J, additional, Pinto, Y M, additional, Wachter, R, additional, Hasenfuss, G, additional, Hermann-Lingen, C, additional, Pieske, B, additional, and Edelmann, F, additional
- Published
- 2018
- Full Text
- View/download PDF
11. Circulating miRNAs as a prognostic tool for heart failure related morbidity and mortality in patients suffering from stable HFpEF: A subgroup analysis of the ALDO-DHF trial
- Author
-
Petutschnigg, J., primary, De Ronde, M.W.J., additional, Trippel, T.D., additional, Bobenko, A., additional, Schleussner, L., additional, Bähr, F., additional, Hashemi, D., additional, Holzendorf, V., additional, Leenders, J.J., additional, Pinto, Y.M., additional, Wachter, R., additional, Hasenfuss, G., additional, Herrmann-Lingen, C., additional, Pieske, B., additional, and Edelmann, F., additional
- Published
- 2018
- Full Text
- View/download PDF
12. P5271Non-invasive monitoring of peripheral and cardiac influence on exercise limitation in patients with heart failure with preserved ejection fraction
- Author
-
Beckmann, S.B., primary, Weisrock, F., additional, Fritschka, M., additional, Wagner, J., additional, Hashemi, D., additional, Tahirovic, E., additional, Radenovic, S., additional, Busjahn, A., additional, Pieske, B., additional, Krahn, T., additional, Dinh, W., additional, and Duengen, H.D., additional
- Published
- 2017
- Full Text
- View/download PDF
13. P1082The history of syncope in heart failure. Mortality increases - but not in all
- Author
-
Hashemi, D., primary, Blum, M., additional, Kraft, R., additional, Mende, M., additional, Stoerk, S., additional, Angermann, C.E., additional, Pankuweit, S., additional, Wachter, R., additional, Edelmann, F., additional, Pieske, B., additional, and Duengen, H.D., additional
- Published
- 2017
- Full Text
- View/download PDF
14. P1486Syncopes in heart failure - Robust predictor in all patients?
- Author
-
Hashemi, D., primary, Blum, M., additional, Mende, M., additional, Stoerk, S., additional, Angermann, CE., additional, Pankuweit, S., additional, Pieske, B., additional, Wachter, R., additional, and Duengen, HD., additional
- Published
- 2017
- Full Text
- View/download PDF
15. Using Interface Waves for Monitoring Fatigue Damage Development in Adhesively Bonded Joints.
- Author
-
Kline, R.A. and Hashemi, D.
- Published
- 1985
- Full Text
- View/download PDF
16. Range variability in cmr feature tracking multilayer strain across different stages of heart failure
- Author
-
Radu Tanacli, Andreas Schuster, Tomas Lapinskas, Gianni Pedrizzetti, Burkert Pieske, Sebastian Kelle, Eike Nagel, Hans-Dirk Düngen, Frank Edelmann, Djawid Hashemi, Rolf Gebker, Tanacli, R., Hashemi, D., Lapinskas, T., Edelmann, F., Gebker, R., Pedrizzetti, G., Schuster, A., Nagel, E., Pieske, B., Dungen, H. -D., and Kelle, S.
- Subjects
Male ,Contraction (grammar) ,616.12-008.46 [udc] ,lcsh:Medicine ,030204 cardiovascular system & hematology ,030218 nuclear medicine & medical imaging ,0302 clinical medicine ,Risk Factors ,Image Processing, Computer-Assisted ,Longitudinal Studies ,Prospective Studies ,lcsh:Science ,cardiac deformation ,Multidisciplinary ,Ejection fraction ,Cardiac cycle ,Middle Aged ,Magnetic Resonance Imaging ,Cardiac hypertrophy ,Cardiology ,cardiovascular mechanics ,cardiac imaging ,Female ,medicine.medical_specialty ,Heart failure ,Heart ventricles ,physiopathology ,Myocardium ,pathology ,Magnetic resonance imaging, cine ,methods ,cardiovascular mechanic ,Article ,03 medical and health sciences ,Heart Failure ,Internal medicine ,medicine ,Humans ,Decompensation ,ddc:610 ,Ventricular remodeling ,Aged ,business.industry ,lcsh:R ,Stroke Volume ,medicine.disease ,Computational biology and bioinformatics ,Feature tracking ,lcsh:Q ,Cardiac magnetic resonance ,business - Abstract
Heart failure (HF) is associated with progressive ventricular remodeling and impaired contraction that affects distinctly various regions of the myocardium. Our study applied cardiac magnetic resonance (CMR) feature tracking (FT) to assess comparatively myocardial strain at 3 distinct levels: subendocardial (Endo-), mid (Myo-) and subepicardial (Epi-) myocardium across an extended spectrum of patients with HF. 59 patients with HF, divided into 3 subgroups as follows: preserved ejection fraction (HFpEF, N = 18), HF with mid-range ejection fraction (HFmrEF, N = 21), HF with reduced ejection fraction (HFrEF, N = 20) and a group of age- gender- matched volunteers (N = 17) were included. Using CMR FT we assessed systolic longitudinal and circumferential strain and strain-rate at Endo-, Myo- and Epi- levels. Strain values were the highest in the Endo- layer and progressively lower in the Myo- and Epi- layers respectively, this gradient was present in all the patients groups analyzed but decreased progressively in HFmrEF and further on in HFrEF groups. GLS decreased with the severity of the disease in all 3 layers: Normal > HFpEF > HFmrEF > HFrEF (Endo-: −23.0 ± 3.5 > −20.0 ± 3.3 > −16.4 ± 2.2 > −11.0 ± 3.2, p −17.5.0 ± 2.6 > −14.5 ± 2.1 > −9.6 ± 2.7, p −12.2 ± 2.1 > −10.6 ± 2.3 > −7.7 ± 2.3, p HFmrEF > HFrEF (Endo-: −34.5 ± 6.2 > −20.0 ± 4.2 > 12.3 ± 4.2, p −13.0 ± 3.4 > −8.0 ± 2.7. p −7.9 ± 2.3 > −4.5 ± 1.9. p
- Published
- 2019
17. Can We Predict Who Will Experience Adverse Events While Using Smoking Cessation Pharmacotherapy? A Secondary Analysis of the EAGLES Clinical Trial.
- Author
-
Wolf BJ, Gray KM, Dahne JR, Hashemi D, and Tomko RL
- Abstract
Introduction: Concerns about potential side effects remain a barrier to uptake of Food and Drug Administration (FDA)-approved smoking cessation pharmacotherapy [i.e., varenicline, bupropion, nicotine replacement therapy (NRT)]. However, use of pharmacotherapy can double the odds of successful quitting. Knowledge of an individual's likelihood of side effects while taking smoking cessation pharmacotherapy could influence treatment planning discussions and monitoring., Methods: We conducted a secondary, post-hoc analysis to predict an individual's likelihood of adverse events (AEs) using the Evaluating Adverse Events in a Global Smoking Cessation Study (EAGLES) data from 4,209 adults in the United States who smoked. Participants were randomized to receive 12 weeks of treatment with varenicline, bupropion, NRT patch, or placebo. Our models predicted the likelihood of moderate to severe psychiatric and non-psychiatric AEs during treatment., Results: Using pre-treatment demographic and clinical data, multivariable logistic regression models yielded acceptable areas under the receiver operating characteristic curve for an individual's likelihood of moderate to severe 1) psychiatric AEs for bupropion and NRT and 2) non-psychiatric AEs for varenicline and bupropion. Once we adjusted for demographic and baseline characteristics, medication was not associated with psychiatric AEs. Varenicline differed from placebo with regards to non-psychiatric AEs., Conclusions: It is possible to predict person-specific likelihood of moderate to severe psychiatric and non-psychiatric AEs during smoking cessation treatment, though the probability of psychiatric AEs did not differ by medication. Future work should consider factors related to implementation in clinical settings, including determining whether lower burden assessment protocols can be equally accurate for AE prediction., Implications: Using data from a large dataset people who smoke in the U.S., it is possible to predict an individual's likelihood of psychiatric and non-psychiatric adverse events during smoking cessation treatment prior to initiating treatment. These predictive models provide a starting point for future work addressing how best to modify and integrate such clinical decision support algorithms into treatment for smoking cessation., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Research on Nicotine and Tobacco. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)
- Published
- 2024
- Full Text
- View/download PDF
18. A molecular dynamics simulation study of thermal conductivity of plumbene.
- Author
-
Mohammadi R, Karimi B, Kieffer J, and Hashemi D
- Abstract
We investigate the lattice thermal conductivity of plumbene using molecular dynamics simulations, overcoming existing limitations by optimizing the parameters of Tersoff and Stillinger-Weber potentials via artificial neural networks. Our findings indicate that at room temperature, the thermal conductivity of a 1050 Å × 300 Å plumbene sheet is approximately 8 W m
-1 K-1 , significantly lower (23%) than that of bulk lead. Our analysis elucidates that thermal conductivity is enhanced by increased sample length, while it is reduced by temperature. Moreover, plumbene samples with zigzag edges display superior thermal conductivity compared to those with armchair edges. In addition, the thermal conductivity of plumbene exhibits an increase at low tensile strains, whereas it decreases as the strains become larger. This investigation provides crucial insights into the thermal conductivity behavior of plumbene under varying conditions.- Published
- 2024
- Full Text
- View/download PDF
19. The beneficial effects of Akkermansia muciniphila and its derivatives on pulmonary fibrosis.
- Author
-
Keshavarz Aziziraftar S, Bahrami R, Hashemi D, Shahryari A, Ramezani A, Ashrafian F, and Siadat SD
- Subjects
- Animals, Male, Mice, Diet, High-Fat adverse effects, Lung pathology, Lung microbiology, Lung drug effects, Lung metabolism, Carbon Tetrachloride, Disease Models, Animal, Extracellular Vesicles metabolism, Probiotics pharmacology, Probiotics therapeutic use, Anti-Inflammatory Agents pharmacology, Akkermansia, Pulmonary Fibrosis microbiology, Pulmonary Fibrosis pathology, Pulmonary Fibrosis drug therapy, Pulmonary Fibrosis metabolism, Mice, Inbred C57BL, Gastrointestinal Microbiome drug effects
- Abstract
Pulmonary fibrosis (PF) is a progressive and debilitating respiratory condition characterized by excessive deposition of extracellular matrix proteins and scarring within the lung parenchyma. Despite extensive research, the pathogenesis of PF remains incompletely understood, and effective therapeutic options are limited. Emerging evidence suggests a potential link between gut microbiota dysbiosis and the development of PF, highlighting the gut-lung axis as a promising therapeutic target. Akkermansia muciniphila (A. muciniphila), a mucin-degrading bacterium residing in the gut mucosal layer, has garnered considerable interest due to its immunomodulatory and anti-inflammatory properties. This study investigates the therapeutic potential of live and pasteurized A. muciniphila, as well as its extracellular vesicles (EVs), in mitigating inflammation and fibrosis in a murine model of carbon tetrachloride (CCl4)-induced PF exacerbated by a high-fat diet (HFD). Male C57BL/6 mice were divided into groups receiving either a normal diet or an HFD, with or without CCl4 administration. The mice were then treated with live or pasteurized A. muciniphila, or its EVs. Lung tissue was analyzed for the expression of inflammatory markers and fibrosis markers using real-time PCR and ELISA. Administration of live and pasteurized A. muciniphila, as well as its EVs, significantly downregulated the expression of inflammatory and fibrosis markers in the lung tissue of CCl4-induced PF mice. Furthermore, these treatments ameliorated the increased production of IL-6 and reduced IL-10 levels observed in the HFD and CCl4-treated groups. These findings suggest that A. muciniphila and its derivatives exert protective effects against pulmonary inflammation and fibrosis, potentially through modulation of the gut-lung axis. The study highlights the therapeutic potential of A. muciniphila and its derivatives as novel interventions for the management of PF, warranting further preclinical and clinical investigations., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
20. Effects of β-hydroxy-β-methylbutyrate (HMB) supplementation on lipid profile in adults: a GRADE-assessed systematic review and meta-analysis of randomized controlled trials.
- Author
-
Sadeghi B, Bahari H, Jozi H, Hasanzadeh MA, Hashemi D, and Bideshki MV
- Abstract
Background and Aim: The regulation of lipid metabolism is crucial for preventing cardiovascular diseases, which are among the leading causes of mortality worldwide. β-hydroxy-β-methylbutyrate (HMB) has garnered attention for its potential role in modulating lipid profiles. However, the magnitude of these effects are unclear due to the heterogeneity of the studies. This study aimed to provide a comprehensive overview of the randomized controlled trials (RCTs) that have examined the effects of HMB on lipid profiles in adults., Methods: Databases including PubMed, Web of Science, and Scopus, were searched for relevant studies through January 2024. The study protocol was also registered at Prospero (no. CRD42024528549). Based on a random-effects model, we calculated WMDs and 95% confidence intervals (CIs). The outcomes assessed included total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C). Sensitivity, subgroup and meta-regression analyses were also conducted., Results: Our analysis included a total of 10 RCTs comprising 421 participants. The pooled data revealed no significant effect of HMB supplementation on TC (WMD: -2.26 mg/dL; 95%CI: -6.11 to 1.58; p = 0.25), TG (WMD: -2.83 mg/dL 95% CI: -12.93 to 7.27; p = 0.58), LDL-C (WMD: 0.13 mg/dL; 95%CI: -3.02 to 3.28; mg; p = 0.94), and HDL-C (WMD: -0.78 mg/dL; 95%CI: -2.04 to 0.48; p = 0.22). The quality of evidence was rated as moderate to low for all outcomes., Conclusion: The current evidence from RCTs suggests that HMB supplementation does not significantly alter lipid profiles, including TC, TG, LDL-C, and HDL-C. Further research is warranted to confirm these results and explore the potential mechanisms of action of HMB., Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=528549, CRD42024528549., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Sadeghi, Bahari, Jozi, Hasanzadeh, Hashemi and Bideshki.)
- Published
- 2024
- Full Text
- View/download PDF
21. A simplified approach to discriminate between healthy subjects and patients with heart failure using cardiac magnetic resonance myocardial deformation imaging.
- Author
-
Witt UE, Müller ML, Beyer RE, Wieditz J, Salem S, Hashemi D, Chen W, Cvetkovic M, Nolden AC, Doeblin P, Blum M, Thiede G, Huppertz A, Steen H, Remppis BA, Falk V, Friede T, and Kelle S
- Abstract
Aims: Left ventricular global longitudinal strain (LV-GLS) shows promise as a marker to detect early heart failure (HF). This study sought to (i) establish cardiac magnetic resonance imaging (CMR)-derived LV-GLS cut-offs to differentiate healthy from HF for both acquisition-based and post-processing techniques, (ii) assess agreement, and (iii) provide a method to convert LV-GLS between both techniques., Methods and Results: A secondary analysis of a prospective study enrolling healthy subjects ( n = 19) and HF patients ( n = 56) was conducted. LV-GLS was measured using fast strain-encoded imaging (fSENC) and feature tracking (FT). Receiver operating characteristic (ROC) analyses were performed to derive and evaluate LV-GLS cut-offs discriminating between healthy, HF with mild deformation impairment (DI), and HF with severe DI. Linear regression and Bland-Altman analyses assessed agreement. Cut-offs discriminating between healthy and HF were identified at -19.3% and -15.1% for fSENC and FT, respectively. Cut-offs of -15.8% (fSENC) and -10.8% (FT) further distinguished mild from severe DI. No significant differences in area under ROC curve were identified between fSENC and FT. Bland-Altman analysis revealed a bias of -4.01%, 95% CI -4.42, -3.50 for FT, considering fSENC as reference. Linear regression suggested a factor of 0.76 to rescale fSENC-derived LV-GLS to FT. Using this factor on fSENC-derived cut-offs yielded rescaled FT LV-GLS cut-offs of -14.7% (healthy vs. HF) and -12% (mild vs. severe DI)., Conclusion: LV-GLS distinguishes healthy from HF with high accuracy. Each measurement technique requires distinct cut-offs, but rescaling factors facilitate conversion. An FT-based LV-GLS ≥ -15% simplifies HF detection in clinical routine., (© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.)
- Published
- 2024
- Full Text
- View/download PDF
22. Heart failure with preserved ejection fraction: diagnosis, risk assessment, and treatment.
- Author
-
von Haehling S, Assmus B, Bekfani T, Dworatzek E, Edelmann F, Hashemi D, Hellenkamp K, Kempf T, Raake P, Schütt KA, Wachter R, Schulze PC, Hasenfuss G, Böhm M, and Bauersachs J
- Subjects
- Humans, Risk Assessment, Ventricular Function, Left physiology, Heart Failure diagnosis, Heart Failure physiopathology, Stroke Volume physiology
- Abstract
The aetiology of heart failure with preserved ejection fraction (HFpEF) is heterogenous and overlaps with that of several comorbidities like atrial fibrillation, diabetes mellitus, chronic kidney disease, valvular heart disease, iron deficiency, or sarcopenia. The diagnosis of HFpEF involves evaluating cardiac dysfunction through imaging techniques and assessing increased left ventricular filling pressure, which can be measured directly or estimated through various proxies including natriuretic peptides. To better narrow down the differential diagnosis of HFpEF, European and American heart failure guidelines advocate the use of different algorithms including comorbidities that require diagnosis and rigorous treatment during the evaluation process. Therapeutic recommendations differ between guidelines. Whilst sodium glucose transporter 2 inhibitors have a solid evidence base, the recommendations differ with regard to the use of inhibitors of the renin-angiotensin-aldosterone axis. Unless indicated for specific comorbidities, the use of beta-blockers should be discouraged in HFpEF. The aim of this article is to provide an overview of the current state of the art in HFpEF diagnosis, clinical evaluation, and treatment., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
23. Reduced dynamic changes in pulmonary artery compliance during isometric handgrip exercise in patients with heart failure.
- Author
-
Hashemi D, Hou X, Doeblin P, Weiß J, Beyer R, Neye M, Erley J, Bucius P, Tanacli R, Kuehne T, Kelm M, Blum M, Edelmann F, Kuebler WM, Düngen HD, Schuster A, Stoiber L, and Kelle S
- Subjects
- Humans, Male, Female, Middle Aged, Aged, Hemodynamics physiology, Prospective Studies, Case-Control Studies, Exercise Tolerance physiology, Compliance, Heart Failure physiopathology, Hand Strength physiology, Pulmonary Artery physiopathology, Exercise physiology
- Abstract
Exercise intolerance is a debilitating symptom in heart failure (HF), adversely affecting both quality of life and long-term prognosis. Emerging evidence suggests that pulmonary artery (PA) compliance may be a contributing factor. This study aims to non-invasively assess PA compliance and its dynamic properties during isometric handgrip (HG) exercise in HF patients and healthy controls, using cardiovascular magnetic resonance (CMR). We prospectively enrolled 36 subjects, comprising 17 HF patients (NYHA class II and III) and 19 healthy controls. Participants performed an HG test, and we assessed changes in PA compliance and hemodynamic flow parameters using advanced CMR techniques. We also explored the relationship between CMR-derived PA compliance metrics and established clinical indicators, ensuring the validity of our findings through intra- and interobserver agreements. HF patients had significantly lower resting PA compliance compared to controls (28.9% vs. 50.1%, p < 0.01). During HG exercise, HF patients exhibited a dampened adaptability in PA compliance. Hemodynamic responses, including heart rate and blood pressure, were not significantly different between the groups. Further analyses revealed a significant correlation between changes in PA compliance and functional capacity, and an inverse relationship with NYHA class. Our study demonstrates a marked difference in PA vascular responses during HG exercise between HF patients and healthy controls. The compromised adaptability in PA compliance in HF patients is correlated with diminished functional capacity. These findings have significant clinical implications and may guide future interventional strategies in HF management., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
24. CMR-based cardiac phenotyping in different forms of heart failure.
- Author
-
Lange T, Backhaus SJ, Schulz A, Hashemi D, Evertz R, Kowallick JT, Hasenfuß G, Kelle S, and Schuster A
- Subjects
- Humans, Male, Female, Middle Aged, Aged, Case-Control Studies, Fibrosis, Ventricular Remodeling, Adult, Reproducibility of Results, Atrial Remodeling, Contrast Media administration & dosage, Heart Failure physiopathology, Heart Failure diagnostic imaging, Ventricular Function, Left, Stroke Volume, Phenotype, Predictive Value of Tests, Atrial Function, Left, Magnetic Resonance Imaging, Cine
- Abstract
Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanistic insights into different HF groups comprising preserved (HFpEF), mid-range (HFmrEF) and reduced ejection fraction (HFrEF). 22 HFpEF, 17 HFmrEF and 15 HFrEF patients as well as 19 healthy volunteers were included. CMR image assessment contained left atrial (LA) and left ventricular (LV) volumetric evaluation as well as left atrioventricular coupling index (LACI). Furthermore, CMR feature-tracking included LV and LA strain in terms of reservoir (Es), conduit (Ee) and active boosterpump (Ea) function. CMR-based tissue characterization comprised T1 mapping as well as late-gadolinium enhancement (LGE) analyses. HFpEF patients showed predominant atrial impairment (Es 20.8%vs.25.4%, p = 0.02 and Ee 8.3%vs.13.5%, p = 0.001) and increased LACI compared to healthy controls (14.5%vs.23.3%, p = 0.004). Patients with HFmrEF showed LV enlargement but mostly preserved LA function with a compensatory increase in LA boosterpump (LA Ea: 15.0%, p = 0.049). In HFrEF LA and LV functional impairment was documented (Es: 14.2%, Ee: 5.4% p < 0.001 respectively; Ea: 8.8%, p = 0.02). This was paralleled by non-invasively assessed progressive fibrosis (T1 mapping and LGE; HFrEF > HFmrEF > HFpEF). CMR-imaging reveals insights into HF phenotypes with mainly atrial affection in HFpEF, ventricular affection with atrial compensation in HFmrEF and global impairment in HFrEF paralleled by progressive LV fibrosis. These data suggest a necessity for a personalized HF management based on imaging findings for future optimized patient management., (© 2024. The Author(s).)
- Published
- 2024
- Full Text
- View/download PDF
25. Deployment of a Digital Advance Care Planning Platform at an Accountable Care Organization.
- Author
-
Roberts RL, Mohan DP, Cherry KD, Sanky S, Huffman TR, Lukasko C, Comito A, Hashemi D, Menn ZK, Fofanova TY, and Andrieni JD
- Subjects
- Humans, Retrospective Studies, Quality of Life, Accountable Care Organizations, Advance Care Planning
- Abstract
Background: Advance care planning (ACP), a process of sharing one's values and preferences for future medical treatments, can improve quality of life, reduce loved ones' anxiety, and decrease unwanted medical utilization and costs. Despite benefits to patients and health care systems, ACP uptake often remains low, due partially to lack of knowledge and difficulty initiating discussions. Digital tools may help reduce these barriers to entry., Methods: We retrospectively examined data from pilot deployment of Koda Health patient-facing ACP among Houston Methodist Coordinated Care patients, for quality improvement (QI) purposes. Patients referred by nurse navigators could access Koda's digital platform, complete ACP, and share the legal documentation generated. Analyzed measures include usage rates and ACP-related decisions within the platform., Results: Of eligible patients (n = 203), 52.7% voluntarily completed their plan. Engagement and completion rates were similar across demographics. Patients indicated majority preference (66.4%) toward spending the last days of life at home. Most patients indicated wanting no life-support intervention if quality of life became unacceptable (51 to 71% across 4 treatments). Life-support decisions were similar between demographic categories, excepting CPR and dialysis, wherein a greater portion of Black patients than White patients preferred at least trial intervention, rather than none., Conclusions: As an observational QI analysis, limitations include bounded geographical reach and lack of data on ACP impacts to subsequent health care utilization, which future studies will address. Findings suggest that digital health tools like Koda can effectively facilitate equitable ACP access and may help support health systems and providers in offering comprehensive ACP., Competing Interests: Conflict of interest: DM, RLR, KC, TF, SS, TH, CL, AC, and DH were each affiliated with Koda Health at the time of work on this project. ZM and JDA have no conflicts of interest to report., (© Copyright by the American Board of Family Medicine.)
- Published
- 2024
- Full Text
- View/download PDF
26. Noninvasive evaluation of pulmonary artery stiffness in heart failure patients via cardiovascular magnetic resonance.
- Author
-
Hou X, Hashemi D, Erley J, Neye M, Bucius P, Tanacli R, Kühne T, Kelm M, Motzkus L, Blum M, Edelmann F, Kuebler WM, Pieske B, Düngen HD, Schuster A, Stoiber L, and Kelle S
- Subjects
- Adult, Humans, Pulmonary Artery diagnostic imaging, Pulse Wave Analysis, Stroke Volume physiology, Magnetic Resonance Spectroscopy, Prognosis, Heart Failure
- Abstract
Heart failure (HF) presents manifestations in both cardiac and vascular abnormalities. Pulmonary hypertension (PH) is prevalent in up 50% of HF patients. While pulmonary arterial hypertension (PAH) is closely associated with pulmonary artery (PA) stiffness, the association of HF caused, post-capillary PH and PA stiffness is unknown. We aimed to assess and compare PA stiffness and blood flow hemodynamics noninvasively across HF entities and control subjects without HF using CMR. We analyzed data of a prospectively conducted study with 74 adults, including 55 patients with HF across the spectrum (20 HF with preserved ejection fraction [HFpEF], 18 HF with mildly-reduced ejection fraction [HFmrEF] and 17 HF with reduced ejection fraction [HFrEF]) as well as 19 control subjects without HF. PA stiffness was defined as reduced vascular compliance, indicated primarily by the relative area change (RAC), altered flow hemodynamics were detected by increased flow velocities, mainly by pulse wave velocity (PWV). Correlations between the variables were explored using correlation and linear regression analysis. PA stiffness was significantly increased in HF patients compared to controls (RAC 30.92 ± 8.47 vs. 50.08 ± 9.08%, p < 0.001). PA blood flow parameters were significantly altered in HF patients (PWV 3.03 ± 0.53 vs. 2.11 ± 0.48, p < 0.001). These results were consistent in all three HF groups (HFrEF, HFmrEF and HFpEF) compared to the control group. Furthermore, PA stiffness was associated with higher NT-proBNP levels and a reduced functional status. PA stiffness can be assessed non-invasively by CMR. PA stiffness is increased in HFrEF, HFmrEF and HFpEF patients when compared to control subjects.Trial registration The study was registered at the German Clinical Trials Register (DRKS, registration number: DRKS00015615)., (© 2023. The Author(s).)
- Published
- 2023
- Full Text
- View/download PDF
27. Cannabis Use Disorder in Adolescents.
- Author
-
Hashemi D and Gray K
- Subjects
- Humans, Adolescent, Marijuana Abuse complications, Marijuana Abuse psychology, Substance-Related Disorders, Cannabis adverse effects
- Abstract
With increasing cannabis potency, increasing variety of methods of cannabis use, and lower perceived risk of cannabis use, it is increasingly important clinicians who work with adolescents remain up-to-date on the latest literature regarding cannabis use and its associated outcomes. Adolescent cannabis use is associated with chronic cognitive, psychosocial, psychiatric, and physical outcomes. Clinicians working in this field should be able to recognize cannabis use disorder, understand how adolescent cannabis use can impact the developing mind, and have informed discussions with patients and families regarding risks of use., (Copyright © 2023 Elsevier Inc. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
28. Quantification of myocardial extracellular volume without blood sampling.
- Author
-
Chen W, Faragli A, Goetze C, Zieschang V, Weiss KJ, Hashemi D, Beyer R, Hafermann L, Stawowy P, Kelle S, and Doeblin P
- Abstract
Aims: Cardiac magnetic resonance (CMR) T 1 relaxation time mapping is an established technique primarily used to identify diffuse interstitial fibrosis and oedema. The myocardial extracellular volume (ECV) can be calculated from pre- and post-contrast T 1 relaxation times and is a reproducible parametric index of the proportion of volume occupied by non-cardiomyocyte components in myocardial tissue. The conventional calculation of the ECV requires blood sampling to measure the haematocrit (HCT). Given the high variability of the HCT, the blood collection is recommended within 24 h of the CMR scan, limiting its applicability and posing a barrier to the clinical routine use of ECV measurements. In recent years, several research groups have proposed a method to determine the ECV by CMR without blood sampling. This is based on the inverse relationship between the T 1 relaxation rate ( R 1) of blood and the HCT. Consequently, a 'synthetic' HCT could be estimated from the native blood R 1, avoiding blood sampling., Methods and Results: We performed a review and meta-analysis of published studies on synthetic ECV, as well as a secondary analysis of previously published data to examine the effect of the chosen regression modell on bias. While, overall, a good correlation and little bias between synthetic and conventional ECV were found in these studies, questions regarding its accuracy remain., Conclusion: Synthetic HCT and ECV can provide a 'non-invasive' quantitative measurement of the myocardium's extracellular space when timely HCT measurements are not available and large alterations in ECV are expected, such as in cardiac amyloidosis. Due to the dependency of T 1 relaxation times on the local setup, calculation of local formulas using linear regression is recommended, which can be easily performed using available data., Competing Interests: Conflict of interest: P.D. owns stock of Siemens and Bayer and received a travel grant from the Berlin University Alliance. A.F. is a shareholder of BOCAhealthcare GmbH. S.K. received funding from the DZHK (German Centre for Cardiovascular Research) and by the BMBF (German Ministry of Education and Research) and personal fees from Servier, outside of the current work. S.K. received an unrestricted research grant from Philips Healthcare and received lecture honoraria from Medis, NL. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.)
- Published
- 2023
- Full Text
- View/download PDF
29. Virtual cardiovascular magnetic resonance training proves feasible and effective: survey data from international participants of the CMR Academy Berlin, Germany.
- Author
-
Hashemi D, Doeblin P, Weiss KJ, Schneider-Reigbert M, Beyer RE, Else C, Faragli A, Stehning C, Stawowy P, Petersen SE, Bucciarelli-Ducci C, Hays AG, Frey N, Thiele H, Portmann A, Fleck E, and Kelle S
- Abstract
Aims: This study aims to evaluate the success of the cardiovascular magnetic resonance (CMR) imaging Academy Berlin's transition from in-person to online CMR imaging training during the global pandemic 2020 and to gather recommendations for future courses., Methods and Results: We conducted an online survey targeting CMR course participants from both the pre-pandemic, in-person era and the pandemic, online era of the CMR Academy Berlin. The survey primarily used Likert-type questions to assess participants' experiences and preferences.A total of 61 out of 158 invited participants (38.61%) completed the survey, with 31 (50.82%) being in-person alumni and 30 (49.18%) being online alumni. Both in-person [83.87% (26/31)] and online [83.33% (25/30)] participants rated the course as either 'very good' or 'excellent', and both groups found the course either 'extremely helpful' or 'very helpful'. However, a higher percentage of in-person participants [96.77% (30/31)] felt comfortable asking questions compared to online participants [83.33% (25/30); P = 0.025]. The majority in both groups preferred a written exam [total: 75.41% (46/61); in-person alumni: 77.42% (24/31); online alumni 73.33% (22/30)]. In terms of course format preferences, in-person courses were preferred by both in-person alumni [38.71% (12/31)] and online alumni [60% (18/30)], almost as much as a hybrid format combining in-person and online elements [in-person alumni: 41.94% (13/31), online alumni: 30% (9/30)]., Conclusion: The transition from in-person to online CMR training at the CMR Academy Berlin was successful in maintaining overall satisfaction. However, there is room for improvement in terms of increased interaction, particularly for online participants. Future CMR- and potentially also cardiac computer tomography-courses should consider adopting a hybrid format to accommodate participants' preferences and enhance their learning experience, especially to gain level II competency, whereas level I virtual only might be sufficient., Competing Interests: Conflict of interest: S.K. reports grants and other support by the DZHK (German Center for Cardiovascular Research), partner site Berlin, Philips Healthcare, BioVentrix, Berlin-Chemie, Merck/Bayer, Novartis, Astra Zeneca, Siemens, and Myocardial Solutions outside of the submitted work. S.K. is also on the advisory board for Merck/Bayer, BioVentrix, and Myocardial Solutions., (© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.)
- Published
- 2023
- Full Text
- View/download PDF
30. Half-Dose versus Single-Dose Gadobutrol for Extracellular Volume Measurements in Cardiac Magnetic Resonance.
- Author
-
Doeblin P, Steinbeis F, Witzenrath M, Hashemi D, Chen W, Weiss KJ, Stawowy P, and Kelle S
- Abstract
Background: Cardiac magnetic resonance (CMR) imaging with gadolinium-based contrast agents offers unique non-invasive insights into cardiac tissue composition. Myocardial extracellular volume (ECV) has evolved as an objective and robust parameter with broad diagnostic and prognostic implications. For the gadolinium compound gadobutrol, the recommended dose for cardiac imaging, including ECV measurements, is 0.1 mmol/kg (single dose). This dose was optimized for late enhancement imaging, a measure of focal fibrosis. Whether a lower dose is sufficient for ECV measurements is unknown. We aim to evaluate the accuracy of ECV measurements using a half dose of 0.05 mmol/kg gadobutrol compared to the standard single dose of 0.1 mmol/kg., Methods and Results: From a contemporary trial (NCT04747366, registered 10 February 2021), a total of 25 examinations with available T1 mapping before and after 0.05 and 0.1 mmol/kg gadobutrol were analyzed. ECV values were calculated automatically from pre- and post-contrast T1 relaxation times. T1 and ECV Measurements were performed in the midventricular septum. ECV values after 0.05 and 0.1 mmol/kg gadobutrol were correlated (R
2 = 0.920, p < 0.001). ECV values after 0.05 mmol/kg had a bias of +0.9% (95%-CI [0.4; 1.4], p = 0.002) compared to 0.1 mmol/kg gadobutrol, with limits of agreement from -1.5 to 3.3%., Conclusions: CMR with a half dose of 0.05 mmol/kg gadobutrol overestimated ECV by 0.9% compared with a full dose of 0.1 mmol/kg, necessitating adjustment of normal values when using half-dose ECV imaging.- Published
- 2023
- Full Text
- View/download PDF
31. Moving toward gender equity in the cardiology and cardiovascular research workforce in Germany: a report from the German Cardiac Society.
- Author
-
Lerchenmüller C, Zelarayan L, Streckfuss-Bömeke K, Gimenez MR, Schnabel R, Hashemi D, Baldus S, Rudolph TK, and Morbach C
- Abstract
Aims: Although the share of women in cardiology in Germany is growing steadily, this does not translate into leadership positions. Medical societies play a crucial role in shaping the national and international medical and scientific environment. The German Cardiac Society (DGK) aims to serve the public discourse on gender-equity by systematic analysis of data on gender representation within the society and in Germany., Methods and Results: We present gender disaggregated data collection of members, official organs, working groups, scientific meetings, as well as awards of the DGK based on anonymized exports from the DGK office as well as on data gathered from the DGK web page. From 2000 to 2020, the overall number of DGK members as well as the share of women increased (12.5% to 25.3%). In 2021, the share of women ranged from 40% to 50% in earlier career stages but was substantially lower at senior levels (23.9% of consulting/attending physicians, 7.1% of physicians-in-chief, 3.4% of directors). The share of women serving in DGK working groups had gained overall proportionality, but nuclei and speaker positions were largely held by men. Boards and project groups were predominantly represented by men as well. At the DGK-led scientific meetings, women contributed more often in junior relative to (invited) senior roles., Conclusion: Increasing numbers of women in cardiology and in the DGK over the past 20 years did not translate into the respective increase in representation of women in leadership positions. There is an urgent need to identify and, more importantly, to overcome barriers towards gender equity. Transparent presentation of society-related data is the first step for future targeted actions in this regard., Competing Interests: Conflict of interest: There are no conflicts of interest regarding the present work., (© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.)
- Published
- 2023
- Full Text
- View/download PDF
32. ADHD symptoms and smoking outcomes in a randomized controlled trial of varenicline for adolescent and young adult tobacco cessation.
- Author
-
Green R, Baker NL, Ferguson PL, Hashemi D, and Gray KM
- Subjects
- Humans, Adolescent, Young Adult, Adult, Varenicline therapeutic use, Treatment Outcome, Double-Blind Method, Tobacco Use Cessation, Attention Deficit Disorder with Hyperactivity psychology, Cigarette Smoking
- Abstract
Background: Most adult daily smokers try their first cigarette during adolescence. Attention-Deficit Hyperactivity Disorder (ADHD) in adolescents is associated with increased risk for cigarette smoking. The impact of ADHD symptoms on smoking cessation among adolescents has been less well-studied. The present secondary data analysis from a clinical trial of varenicline examined ADHD symptoms as a moderator of smoking cessation in adolescents and young adults., Methods: The double-blind, placebo-controlled trial included treatment-seeking daily cigarette smokers ages 14 - 21 (N = 157) randomized to receive a 12-week course of varenicline or placebo, added to weekly smoking cessation counseling. At pre-treatment assessment, participants were administered a self-report measure of ADHD symptoms, the ADHD - Rating Scale (ADHD-RS). High (≥5) versus low (<5) and continuous ADHD-RS symptom counts in both hyperactive/impulsive (HI) and inattention (IA) domains were examined as predictors of smoking outcomes., Results: Participants with high IA symptoms at baseline were less likely to achieve 7-day point prevalence abstinence (PPA) at weekly visits (p = .001) during active treatment and end-of-treatment (p = .002) compared to those with low IA symptoms. In contrast, high HI symptoms did not predict differences in 7-day PPA or end-of-treatment abstinence versus low symptoms (p's ≥ .07). These findings were not modified by varenicline versus placebo treatment assignment., Conclusions: ADHD IA symptoms were associated with poorer cessation outcomes among adolescent smokers. These findings warrant additional investigation into how ADHD symptoms may be accounted for in smoking cessation interventions for adolescents and young adults., (Published by Elsevier B.V.)
- Published
- 2023
- Full Text
- View/download PDF
33. Cutaneous Surgical Wounds Have Distinct Microbiomes from Intact Skin.
- Author
-
Gupta S, Poret AJ, Hashemi D, Eseonu A, Yu SH, D'Gama J, Neel VA, and Lieberman TD
- Subjects
- Humans, Staphylococcus aureus, Skin microbiology, Bacteria, Surgical Wound, Microbiota, Skin Neoplasms
- Abstract
Infections are relatively rare following cutaneous surgical procedures, despite the potential for wound exposure to pathogens both during surgery and throughout the healing process. Although gut commensals are believed to reduce the risk of intestinal infections, an analogous role for skin commensals has not been described. In fact, the microbiome of normally healing surgical skin wounds has not yet been profiled using culture-independent techniques. We characterized the wound microbiome in 53 patients who underwent skin cancer surgery and healed without signs or symptoms of infection. A week after surgery, several bacterial species displayed significant differences in relative abundance when compared to control, nonoperated skin from the same patient. The relative abundance of the most common bacterium found on intact skin, Cutibacterium acnes, was reduced in wounds 5-fold. Staphylococcus aureus, a frequent cause of postoperative skin infections, was enriched 6.4-fold in clinically noninfected wounds, suggesting active suppression of pathogenicity. Finally, members of the Corynebacterium genus were the dominant organism in postoperative wounds, making up 37% of the average wound microbiome. The enrichment of these bacteria in normally healing wounds suggests that they might be capable of providing colonization resistance. Future studies focused on the biological and clinical significance of the wound microbiome may shed light on normal wound healing and potential therapeutic opportunities to mitigate infection risk. IMPORTANCE Commensal bacteria on skin may limit the ability of pathogenic bacteria to cause clinically significant infections. The bacteria on healing acute wounds, which might provide such a protective effect, have not been described using culture-independent approaches in the absence of antibiotics. We compare the microbiome of wounds a week after skin cancer removal surgery with intact skin from the same patient. We find that the potentially pathogenic species S. aureus is common on these healing wounds despite the absence of symptoms or signs of infection. We report that bacteria often considered as potential skin probiotics, including Staphylococcus epidermidis, do not reach high relative abundance in wound microbiomes. In contrast, specific members of the Corynebacterium genus, rarely associated with infections, were significantly enriched in healing wounds compared to intact skin. Future work is needed to see if Corynebacterium species or derivatives thereof could be employed to lower the risk of wound infection.
- Published
- 2023
- Full Text
- View/download PDF
34. Reduced functional capacity is associated with the proportion of impaired myocardial deformation assessed in heart failure patients by CMR.
- Author
-
Hashemi D, Doeblin P, Blum M, Weiss KJ, Schneider M, Beyer R, Pieske B, Duengen HD, Edelmann F, and Kelle S
- Abstract
Aims: Heart failure (HF) does not only reduce the life expectancy in patients, but their life is also often limited by HF symptoms leading to a reduced quality of life (QoL) and a diminished exercise capacity. Novel parameters in cardiac imaging, including both global and regional myocardial strain imaging, promise to contribute to better patient characterization and ultimately to better patient management. However, many of these methods are not part of clinical routine yet, their associations with clinical parameters have been poorly studied. An imaging parameters that also indicate the clinical symptom burden of HF patients would make cardiac imaging more robust toward incomplete clinical information and support the clinical decision process., Methods and Results: This prospective study conducted at two centers in Germany between 2017 and 2018 enrolled stable outpatient subjects with HF [ n = 56, including HF with reduced ejection fraction (HFrEF), HF with mid-range ejection fraction (HFmrEF), and HF with preserved ejection fraction (HFpEF)] and a control cohort ( n = 19). Parameters assessed included measures for external myocardial function, for example, cardiac index and myocardial deformation measurements by cardiovascular magnetic resonance imaging, left ventricular global longitudinal strain (GLS), the global circumferential strain (GCS), and the regional distribution of segment deformation within the LV myocardium, as well as basic phenotypical characteristics including the Minnesota Living with Heart Failure Questionnaire (MLHFQ) and the 6-minute walk test (6MWT). If less than 80% of the LV segments are preserved in their deformation capacity the functional capacity by 6MWT (6 minutes walking distance: MyoHealth ≥ 80%: 579.8 ± 177.6 m; MyoHealth 60-<80%: 401.3 ± 121.7 m; MyoHealth 40-<60%: 456.4 ± 68.9 m; MyoHealth < 40%: 397.6 ± 125.9 m, overall p -value: 0.03) as well as the symptom burden are significantly impaired (NYHA class: MyoHealth ≥ 80%: 0.6 ± 1.1 m; MyoHealth 60-<80%: 1.7 ± 1.2 m; MyoHealth 40-<60%: 1.8 ± 0.7 m; MyoHealth < 40%: 2.4 ± 0.5 m; overall p -value < 0.01). Differences were also observed in the perceived exertion assessed by on the Borg scale (MyoHealth ≥ 80%: 8.2 ± 2.3 m; MyoHealth 60-<80%: 10.4 ± 3.2 m; MyoHealth 40-<60%: 9.8 ± 2.1 m; MyoHealth < 40%: 11.0 ± 2.9 m; overall p -value: 0.20) as well as quality of life measures (MLHFQ; MyoHealth ≥ 80%: 7.5 ± 12.4 m; MyoHealth 60-<80%: 23.4 ± 23.4 m; MyoHealth 40-<60%: 20.5 ± 21.2 m; MyoHealth < 40%: 27.4 ± 24.4 m; overall p -value: 0.15)-while these differences were not significant., Conclusion: The share of LV segments with preserved myocardial contraction promises to discriminate between symptomatic and asymptomatic subjects based on the imaging findings, even when the LV ejection fraction is preserved. This finding is promising to make imaging studies more robust toward incomplete clinical information., Competing Interests: SK reported grants and other support by the Philips Healthcare, BioVentrix, Berlin-Chemie, Merck/Bayer, Novartis, Astra Zeneca, Siemens, and Myocardial Solutions outside of the submitted work. SK was also on the advisory board for Merck/Bayer, BioVentrix, and Myocardial Solutions. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Hashemi, Doeblin, Blum, Weiss, Schneider, Beyer, Pieske, Duengen, Edelmann and Kelle.)
- Published
- 2023
- Full Text
- View/download PDF
35. CMR detects decreased myocardial deformation in asymptomatic patients at risk for heart failure.
- Author
-
Hashemi D, Doeblin P, Blum M, Weiss KJ, Schneider M, Korosoglou G, Beyer RE, Pieske B, Edelmann F, and Kelle S
- Abstract
Aims: The main management strategy of heart failure with preserved ejection fraction (HFpEF) is prevention since HFpEF is associated with many cardiovascular (CV) risk factors, especially since HFpEF is linked to a high risk for both mortality and recurrent heart failure (HF) hospitalizations. Therefore, there is a need for new tools to identify patients with a high risk profile early. Regional strain assessment by CMR seems to be superior in describing deformation impairment in HF. The MyoHealth score is a promising tool to identify cardiac changes early., Methods and Results: Heart failure patients irrespective of LVEF and asymptomatic controls were recruited, and CMR based measures were obtained. For this analysis the asymptomatic control group ( n = 19) was divided into asymptomatic subjects without CV co-morbidities or evidence of cardiac abnormalities and ( n = 12) and asymptomatic subjects with CV co-morbidities or evidence of cardiac abnormalities ( n = 7) as well as patients with HFpEF ( n = 19). We performed CMR scans at rest and during a stress test using isometric handgrip exercise (HG). Assessing the MyoHealth score at rest revealed preserved regional strain in 85 ± 9% of LV segments in controls, 73 ± 11% in at Risk subjects and 73 ± 8% in HFpEF patients. During stress the MyoHealth score was 84 ± 7% in controls, 83 ± 7 in at risk subjects and 74 ± 11 in HFpEF patients., Conclusion: In summary, we show for the first time that asymptomatic subjects with increased CV risk present with HFpEF like impaired myocardial deformation at rest, while they show results like controls under HG stress. The potential of preventive treatment in this group of patients merits further investigation in future., Clinical Trial Registration: [https://drks.de/search/de/trial/DRKS00015615], identifier [DRKS00015615]., Competing Interests: SK reports grants and other support by the DZHK (German Center for Cardiovascular Research), Partner Site Berlin, Philips Healthcare, BioVentrix, Berlin Chemie, Merck/Bayer, Novartis, AstraZeneca, Siemens, and Myocardial Solutions outside of the submitted work. SK was also on the advisory board for Merck/Bayer, BioVentrix, and Myocardial Solutions. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Hashemi, Doeblin, Blum, Weiss, Schneider, Korosoglou, Beyer, Pieske, Edelmann and Kelle.)
- Published
- 2023
- Full Text
- View/download PDF
36. Evaluation of the HFA-PEFF Score: results from the prospective DIAST-CHF cohort.
- Author
-
Hashemi D, Mende M, Trippel TD, Petutschnigg J, Hasenfuss G, Nolte K, Herrmann-Lingen C, Feuerstein A, Langhammer R, Tschöpe C, Pieske B, Wachter R, and Edelmann F
- Subjects
- Humans, Stroke Volume, Prospective Studies, Prognosis, Risk Factors, Heart Failure diagnosis, Heart Failure epidemiology
- Abstract
Aims: Although the number of patients suffering from heart failure with preserved ejection fraction (HFpEF) increases, the routine diagnosis remains a challenge. In the absence of a pathognomonic sign for HFpEF or specific treatment strategies, a prognosis-based characterization of suspected patients remains promising for both the risk stratification of the patients and a disease definition. The Heart Failure Association (HFA) of the European Society of Cardiology has introduced an algorithm with different levels of likelihood regarding the diagnosis of HFpEF, the HFA-PEFF score. We aimed to evaluate the predictive value of this algorithm in a large cohort regarding mortality, symptom burden, and the functional status., Methods and Results: DIAST-CHF is a multicentre, population-based, prospective, observational study in subjects with at least one risk factor for HFpEF between the age of 50 and 85. We calculated the HFA-PEFF score (n = 1668) and analysed the risk groups for overall mortality, cardiovascular hospitalization, and submaximal functional capacity (6-min walk distance) at baseline and after a follow-up period of 10 years. Patients with high HFA-PEFF score values 5&6 showed a higher mortality than those with an intermediate score (score values 2-4) and low score values (high 21.3% vs. intermediate 10.1% vs. low 4.3%, P < 0.001). Also, the burden of MACE (death, cardiovascular hospitalization, new myocardial infarction, first diagnosis of HF) was increased in the high score values group (high 40.7% vs. intermediate 25.9% vs. low 13.9%, P < 0.001). Similarly, patients with higher scores had higher cumulative incidences of cardiovascular hospitalizations (P = 0.011). Subjects with higher scores also had lower 6-min walk distance both at baseline and during follow-up., Conclusions: The HFA-PEFF score provides a reliable instrument to stratify suspected HFpEF patients by their risk for mortality, symptom burden, and functional status in cohort at risk with a follow-up period of 10 years. As high HFA-PEFF scores are associated with worse outcome, the HFA-PEFF algorithm describes a defining approach towards HFpEF., (© 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Published
- 2022
- Full Text
- View/download PDF
37. Editorial: Highlights in Cardiovascular Imaging: 2021.
- Author
-
Hashemi D, Kelle S, Bourantas CV, and Chandrasekharan KH
- Abstract
Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
- Published
- 2022
- Full Text
- View/download PDF
38. AMPK signaling in diabetes mellitus, insulin resistance and diabetic complications: A pre-clinical and clinical investigation.
- Author
-
Entezari M, Hashemi D, Taheriazam A, Zabolian A, Mohammadi S, Fakhri F, Hashemi M, Hushmandi K, Ashrafizadeh M, Zarrabi A, Ertas YN, Mirzaei S, and Samarghandian S
- Subjects
- AMP-Activated Protein Kinases therapeutic use, Animals, Diabetes Complications therapy, Diabetes Mellitus therapy, Humans, Insulin Resistance, Mice, Rats, Signal Transduction, AMP-Activated Protein Kinases metabolism, Diabetes Complications metabolism, Diabetes Mellitus metabolism
- Abstract
Diabetes mellitus (DM) is considered as a main challenge in both developing and developed countries, as lifestyle has changed and its management seems to be vital. Type I and type II diabetes are the main kinds and they result in hyperglycemia in patients and related complications. The gene expression alteration can lead to development of DM and related complications. The AMP-activated protein kinase (AMPK) is an energy sensor with aberrant expression in various diseases including cancer, cardiovascular diseases and DM. The present review focuses on understanding AMPK role in DM. Inducing AMPK signaling promotes glucose in DM that is of importance for ameliorating hyperglycemia. Further investigation reveals the role of AMPK signaling in enhancing insulin sensitivity for treatment of diabetic patients. Furthermore, AMPK upregulation inhibits stress and cell death in β cells that is of importance for preventing type I diabetes development. The clinical studies on diabetic patients have shown the role of AMPK signaling in improving diabetic complications such as brain disorders. Furthermore, AMPK can improve neuropathy, nephropathy, liver diseases and reproductive alterations occurring during DM. For exerting such protective impacts, AMPK signaling interacts with other molecular pathways such as PGC-1α, PI3K/Akt, NOX4 and NF-κB among others. Therefore, providing therapeutics based on AMPK targeting can be beneficial for amelioration of DM., (Copyright © 2021. Published by Elsevier Masson SAS.)
- Published
- 2022
- Full Text
- View/download PDF
39. Influence of baseline parameters on one-year physical, mental, and health-related quality of life in patients with heart failure and preserved ejection fraction.
- Author
-
Fitz J, Edelmann F, Hasenfuß G, Sandek A, Nolte K, Hashemi D, Trippel TD, Wachter R, and Herrmann-Lingen C
- Subjects
- Aged, Female, Health Status, Humans, Middle Aged, Stroke Volume, Ventricular Function, Left, Heart Failure, Quality of Life psychology
- Abstract
Aims: To identify baseline parameters longitudinally influencing overall health-related quality of life (HRQoL), physical function and mental health 1 year later in patients with chronic heart failure and preserved ejection fraction (HFpEF)., Methods and Results: We performed post hoc analyses of the randomized aldosterone in diastolic heart failure (Aldo-DHF) trial, including 422 patients with HFpEF and NYHA class II or III. Overall HRQoL, measured by the Minnesota Living with Heart Failure Questionnaire (MLHFQ), physical functioning and mental health, both measured by the Short Form 36 Health Survey (SF-36), after 12 months were predicted in correlation analyses and multivariate regression analyses with continuous values and worst versus three better HRQoL quartiles as dependent variables. The mean age of the study population was 66.8 ± 7.6 years, 52.4% were female, and 86.0% had NYHA class II. All HRQoL variables at 1 year were predicted by their respective baseline values (all P < 0.001), which were also the best variables to predict lowest versus higher HRQoL quartiles (all P < 0.001). For overall HRQoL, six-minute-walking-distance (P = 0.009), Borg-score (P = 0.001), coronary heart disease (P = 0.036) and SF-36 role-emotional (P = 0.005) independently predicted one-year-outcome, while depression diagnosis (P = 0.044), self-reported health status (P = 0.023) and PHQ depression (P = 0.001) were only significant predictors when excluding MLHFQ total score at baseline. In logistic regression analyses, only SF-36 role-emotional (P = 0.016) independently predicted overall HRQoL group status at follow up. For physical functioning, Borg-score (P ≤ 0.001), 6 min walking distance (P = 0.005), coronary heart disease (P = 0.009), and SF-36 vitality (P = 0.001) were significant independent predictors, also when excluding baseline physical functioning. Low SF-36 vitality (P = 0.021) and presence of coronary heart disease (P = 0.027) independently predicted a patient's membership in the lowest quartile 1 year later. For mental health, SF-36 physical functioning (P = 0.025) and HADS anxiety (P = 0.046) were independent predictors, while self-rated fatigue and poor performance (P = 0.033) and SF-36 vitality (P = 0.008) only served as significant predictors when excluding mental health at baseline. HADS anxiety (P = 0.009) also served as independent predictor of a patient's group status after 1 year., Conclusion: Overall HRQoL, physical functioning, and mental health of HFpEF patients 1 year later are mainly influenced by their respective baseline values. Other self-rated baseline parameters also showed independent effects while objective severity measures had limited predictive value., (© 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Published
- 2021
- Full Text
- View/download PDF
40. [The importance of health-related quality of life at baseline in predicting event-free survival in patients with a cardiovascular risk profile].
- Author
-
Beismann C, Nolte K, Wachter R, Hashemi D, Trippel T, Edelmann F, and Meyer T
- Subjects
- Aged, Heart Disease Risk Factors, Humans, Prognosis, Progression-Free Survival, Quality of Life, Risk Factors, Stroke Volume, Ventricular Function, Left, Cardiovascular Diseases epidemiology, Heart Failure epidemiology
- Abstract
The importance of health-related quality of life at baseline in predicting event-free survival in patients with a cardiovascular risk profile Background: Manifest heart failure impairs all dimensions of health-related quality of life (HRQOL). However, the role of HRQOL in patients with risk factors for the development of heart failure with preserved ejection fraction (HFpEF) is only poorly understood. Objective: In this post-hoc analysis of the DIAST-CHF observational study, we tested the hypothesis whether a lower HRQOL at baseline is prognostically associated with an increase in cardiovascular events during follow-up in elderly patients with a cardiovascular risk profile. Methods: The DIAST-CHF observational study enrolled 1.937 patients aged 50 to 85 years with at least one risk factor for the development of HFpEF. HRQOL was assessed using the German version of the Short-Form-36 (SF-36) Health Survey. Results: Patients with comorbid chronic diseases, including manifest heart failure, coronary artery disease, atrial fibrillation, diabetes mellitus and depression, rated their health status (Self-rated health, SRH) significantly worse than those without comorbidities. Older age, higher body-mass index and elevated serum amino-terminal pro-brain natriuretic peptide (NTproBNP) concentration as well as lower left ventricular ejection fraction (LVEF) and impaired 6-minute walk test showed significant relationships to SRH. Kaplan-Meier analyses and Cox regression models using quartiles of either SF-36 subscales "Physical Component Summary" (PCS) or SRH groups demonstrated significant differences in event-free survival (all-cause death or cardiovascular hospitalization), whereas no difference in event-free survival was observed among the quartiles of the SF-36 subscale "Mental Component Summary" (MCS). Conclusion: In patients with risk factors for the development of HFpEF, HRQOL questionnaires are suitable instruments for risk stratification if they capture physical impairments, rather than psychological limitations of quality of life.
- Published
- 2021
- Full Text
- View/download PDF
41. The role of halogen bonding in metal free phosphors.
- Author
-
Ansari R, Hashemi D, and Kieffer J
- Abstract
The enhanced spin-orbit coupling necessary for phosphorescence is thought to be due to the halogen bonding that is present in the all-organic crystalline systems. To elucidate the underlying mechanism, the electronic and optical properties of purely organic phosphor candidates are investigated using density functional theory calculations. The unit cell structure of a known organic phosphor containing bromine is used to validate the accuracy of the computational methodology. Compared to experiments, the calculated lattice constants deviate by less than 1 percent for each lattice constant. The same computational approach is then used to predict the lattice constants for molecular analogs containing fluorine, chlorine, and iodine. Electronic structure and photonic properties of the predicted crystals are computed. Finally, the presence of halogen bonding is corroborated, with fluorine forming the weakest and iodine the strongest halogen bonding interactions. Our findings demonstrate how computational methods can be effectively used for the predictive design of organic materials in lighting devices.
- Published
- 2021
- Full Text
- View/download PDF
42. Plasma Biomarker Profiling in Heart Failure Patients with Preserved Ejection Fraction before and after Spironolactone Treatment: Results from the Aldo-DHF Trial.
- Author
-
Schnelle M, Leha A, Eidizadeh A, Fuhlrott K, Trippel TD, Hashemi D, Toischer K, Wachter R, Herrmann-Lingen C, Hasenfuß G, Pieske B, Binder L, and Edelmann F
- Subjects
- Heart Failure drug therapy, Hospitalization, Humans, Placebos, Biomarkers blood, Heart Failure blood, Heart Failure physiopathology, Spironolactone therapeutic use, Stroke Volume drug effects
- Abstract
The pathophysiology of heart failure with preserved ejection fraction (HFpEF) is poorly understood and therapeutic strategies are lacking. This study aimed to identify plasma proteins with pathophysiological relevance in HFpEF and with respect to spironolactone-induced effects. We assessed 92 biomarkers in plasma samples from 386 HFpEF patients-belonging to the Aldo-DHF trial-before (baseline, BL) and after one-year treatment (follow up, FU) with spironolactone (verum) or a placebo. At BL, various biomarkers showed significant associations with the two Aldo-DHF primary end point parameters: 33 with E/e' and 20 with peak VO
2 . Ten proteins including adrenomedullin, FGF23 and inflammatory peptides (e.g., TNFRSF11A, TRAILR2) were significantly associated with both parameters, suggesting a role in the clinical HFpEF presentation. For 13 proteins, expression changes from BL to FU were significantly different between verum and placebo. Among them were renin, growth hormone, adrenomedullin and inflammatory proteins (e.g., TNFRSF11A, IL18 and IL4RA), indicating distinct spironolactone-mediated effects. BL levels of five proteins, e.g., inflammatory markers such as CCL17, IL4RA and IL1ra, showed significantly different effects on the instantaneous risk for hospitalization between verum and placebo. This study identified plasma proteins with different implications in HFpEF and following spironolactone treatment. Future studies need to define their precise mechanistic involvement.- Published
- 2021
- Full Text
- View/download PDF
43. Conjugated Copolymers That Shouldn't Be.
- Author
-
Guan J, Sun Z, Ansari R, Liu Y, Endo A, Unno M, Ouali A, Mahbub S, Furgal JC, Yodsin N, Jungsuttiwong S, Hashemi D, Kieffer J, and Laine RM
- Abstract
Multiple studies have explored using cage silsesquioxanes (SQs) as backbone elements in hybrid polymers motivated by their well-defined structures and physical and mechanical properties. As part of this general exploration, we report unexpected photophysical properties of copolymers derived from divinyl double decker (DD) SQs, [vinyl(Me)Si(O
0.5 )2 ][PhSiO1.5 ]8 [(O0.5 )2 Si(Me)vinyl] (vinylDDvinyl). These copolymers exhibit strong emission red-shifts relative to model compounds, implying unconventional conjugation, despite vinyl(Me)Si(O-)2 siloxane bridges. In an effort to identify minimum SQ structures that do/do not offer extended conjugation, we explored Heck catalyzed co-polymerization of vinyl-ladder(LL)-vinyl compounds, vinyl(Me/Ph)Si(O0.5 )2 [PhSiO1.5 ]4 (O0.5 )2 Si(Me/Ph)vinyl, with Br-Ar-Br. Most surprising, the resulting oligomers show 30-60 nm emission red-shifts beyond those seen with vinylDDvinyl analogs despite lacking a true cage. Further evidence for unconventional conjugation includes apparent integer charge transfer (ICT) between LL-co-thiophene, bithiophene, and thienothiophene with 10 mol % F4 TCNQ, suggesting potential as p-type doped organic/inorganic semiconductors., (© 2021 Wiley-VCH GmbH.)- Published
- 2021
- Full Text
- View/download PDF
44. Myocardial deformation assessed among heart failure entities by cardiovascular magnetic resonance imaging.
- Author
-
Hashemi D, Motzkus L, Blum M, Kraft R, Tanacli R, Tahirovic E, Doeblin P, Zieschang V, Zamani SM, Kelm M, Kuehne T, Pieske B, Alogna A, Edelmann F, Duengen HD, and Kelle S
- Subjects
- Germany, Humans, Magnetic Resonance Imaging, Myocardium, Prospective Studies, Stroke Volume, Heart Failure diagnosis
- Abstract
Aims: Although heart failure (HF) is a leading cause for hospitalization and mortality, normalized and comparable non-invasive assessment of haemodynamics and myocardial action remains limited. Moreover, myocardial deformation has not been compared between the guideline-defined HF entities. The distribution of affected and impaired segments within the contracting left ventricular (LV) myocardium have also not been compared. Therefore, we assessed myocardial function impairment by strain in patients with HF and control subjects by magnetic resonance imaging after clinically phenotyping these patients., Methods and Results: This prospective study conducted at two centres in Germany between 2017 and 2018 enrolled stable outpatient subjects with HF [n = 56, including HF with reduced ejection fraction (HFrEF), HF with mid-range ejection fraction (HFmrEF), and HF with preserved ejection fraction (HFpEF)] and a control cohort (n = 12). Parameters assessed included measures for external myocardial function, for example, cardiac index and myocardial deformation measurements by cardiovascular magnetic resonance imaging, left ventricular global longitudinal strain (GLS), the global circumferential strain (GCS) and the regional distribution of segment deformation within the LV myocardium, as well as basic phenotypical characteristics. Comparison of the cardiac indices at rest showed no differences neither between the HF groups nor between the control group and HF patients (one-way ANOVA P = 0.70). The analysis of the strain data revealed differences between all groups in both LV GLS (One-way ANOVA: P < 0.01. Controls vs. HFpEF: -20.48 ± 1.62 vs. -19.27 ± 1.25. HFpEF vs. HFmrEF: -19.27 ± 1.25 vs. -15.72 ± 2.76. HFmrEF vs. HFrEF: -15.72 ± 2.76 vs. -11.51 ± 3.97.) and LV GCS (One-way ANOVA: P < 0.01. Controls vs. HFpEF: -19.74 ± 2.18 vs. -17.47 ± 2.10. HFpEF vs. HFmrEF: -17.47 ± 2.10 vs. -12.78 ± 3.47. HFrEF: -11.41 ± 3.27). Comparing the segment deformation distribution patterns highlighted the discriminating effect between the groups was much more prominent between the groups (one-way ANOVA P < 0.01) when compared by a score combining regional effects and a global view on the LV. Further analyses of the patterns among the segments affected showed that while the LVEF is preserved in HFpEF, the segments impaired in their contractility are located in the ventricular septum. The worse the LVEF is, the more segments are affected, but the septum remains an outstanding location with the most severe contractility impairment throughout the HF entities., Conclusions: While cardiac index at rest did not differ significantly between controls and stable HF patients suffering from HFrEF, HFmrEF, or HFpEF, the groups did differ significantly in LV GLS and LV GCS values. Regional strain analysis revealed that the LV septum is the location affected most, with reduced values already visible in HFpEF and further reductions in HFmrEF and HFrEF., (© 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Published
- 2021
- Full Text
- View/download PDF
45. The diagnostic and prognostic value of galectin-3 in patients at risk for heart failure with preserved ejection fraction: results from the DIAST-CHF study.
- Author
-
Trippel TD, Mende M, Düngen HD, Hashemi D, Petutschnigg J, Nolte K, Herrmann-Lingen C, Binder L, Hasenfuss G, Pieske B, Wachter R, and Edelmann F
- Subjects
- Aged, Biomarkers, Blood Proteins, Female, Galectin 3, Galectins, Humans, Male, Prognosis, Stroke Volume, Heart Failure diagnosis
- Abstract
Aims: Galectin-3 (Gal-3) predicts long-term outcome among patients with heart failure (HF) with preserved ejection fraction (HFpEF). The ability of Gal-3 to diagnose and predict incident HFpEF in a cohort at risk for HFpEF is of particular interest. We aimed to determine the association between Gal-3 and clinical manifestations of HFpEF, the relationship between Gal-3 and all-cause mortality, or the composite of cardiovascular hospitalization and death., Methods and Results: The observational Diast-CHF study included patients aged 50 to 85 years with ≥1 risk factor for HF (e.g. hypertension, diabetes mellitus, and atherosclerotic disease) or previously suspected HF. Patients were followed for 10 years. The association between Gal-3, evidence of diastolic dysfunction, and Framingham criteria for HF was examined. All deaths and hospitalizations were adjudicated as cardiovascular or non-cardiovascular. The analysis population was composed of 1386 subjects (67 years old, 50.9% female). The area under the receiver operating characteristic curve to diagnose HFpEF was 0.71. At a cut-off value of 13.57 ng/mL, sensitivity was 0.61 and specificity was 0.73 for Gal-3, and the diagnostic power to detect HFpEF was superior to N-terminal pro-brain natriuretic peptide (area under the receiver operating characteristic curve 0.59, P > 0.001). Baseline Gal-3 was associated with risk factors for HF (P < 0.001). Higher levels of Gal-3 predicted incident HFpEF (P < 0.05), adjusted all-cause mortality (P < 0.001), and the adjusted composite of cardiovascular hospitalization and death (P < 0.001), both independent from N-terminal pro-brain natriuretic peptide., Conclusions: Gal-3 differentiated patients with HFpEF from an overall cohort of well-characterized patients with risk factors for HFpEF. Independent of other factors, baseline Gal-3 levels were associated with a higher risk for incident HFpEF, mortality, or the composite of cardiovascular hospitalization and death over 10 year follow-up. In conjunction with clinical parameters, Gal-3 adds a statistically significant value for the diagnosis of HFpEF within this study, yet the clinical relevance remains debatable., (© 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Published
- 2021
- Full Text
- View/download PDF
46. Substitutional 4d transition metal doping in atomically thin lead.
- Author
-
Hashemi D and Iizuka H
- Abstract
To study the potential of plumbene as a dilute magnetic semiconductor, we computationally investigate the structural, electronic, and magnetic properties of 4d transition metal (TM) doped plumbene using density functional theory (DFT). These calculations show that Zr, Nb, Mo, Tc-doped plumbene systems are magnetic while no magnetic solution was found for Y, Ru, Rh, and Pd-doped cases. We also calculate the magnetic couplings between two TM impurities in the system with an impurity concentration of less than 2%. Strong exchange couplings and large magnetic anisotropic energies, indicate the potential for spintronics applications., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)
- Published
- 2021
- Full Text
- View/download PDF
47. Multilayer myocardial strain improves the diagnosis of heart failure with preserved ejection fraction.
- Author
-
Tanacli R, Hashemi D, Neye M, Motzkus LA, Blum M, Tahirovic E, Dordevic A, Kraft R, Zamani SM, Pieske B, Düngen HD, and Kelle S
- Subjects
- Heart, Humans, Myocardium, Stroke Volume, Heart Failure diagnosis
- Abstract
Aims: The diagnostic and treatment of patients with heart failure with preserved ejection fraction (HFpEF) are both hampered by an incomplete understanding of the pathophysiology of the disease. Novel imaging tools to adequately identify these patients from individuals with a normal cardiac function and respectively patients with HF with reduced EF are warranted. Computing multilayer myocardial strain with feature tracking is a fast and accurate method to assess cardiac deformation. Our purpose was to assess the HFpEF diagnostic ability of multilayer strain parameters and compare their sensitivity and specificity with other established parameters., Methods and Results: We included 20 patients with a diagnosis of HFpEF and, respectively, 20 matched controls. We assessed using feature-tracking cardiac magnetic resonance longitudinal and circumferential myocardial strain at three distinct layers of the myocardium: subendocardial (Endo-), mid-myocardial (Myo-), and subepicardial (Epi-). Comparatively, we additionally assessed various others clinical, imaging, and biochemical parameters with a putative role in HFpEF diagnostic: left ventricular end-diastolic volume (LVEDV), left ventricular mass (LVM), interventricular septum (IVS) wall thickness and free wall thickness, left atrial volume and strain, septal and lateral mitral annular early diastolic velocity (e`), E/e´ ratio, and plasma levels of N-terminal pro-B-type natriuretic peptide (NT-proBNP). Global longitudinal strain (GLS) is significantly impaired at Endo (-20.8 ± 4.0 vs. -23.2 ± 3.4, P = 0.046), Myo- (-18.0 ± 3.0 vs. -21.0 ± 2.5, P = 0.002), and Epi- (-12.2 ± 2.0 vs. -16.2 ± 2.5, P < 0.001) levels. Compared with any other imaging parameter, an Epi-GLS lower than 13% shows the highest ability to detect patients with HFpEF [area under the curve (AUC) = 0.90 (0.81-1), P < 0.001] and in tandem with NT-proBNP can diagnose with maximal sensibility (93%) and specificity (100%), patients with HFpEF from normal, composed variable [AUC = 0.98 (0.95-1), P < 0.001]. In a logistic regression model, a composite predictive variable taking into account both GLS Epi and NT-proBNP values in each individual subject reached a sensitivity of 89% and a specificity of 100% with an AUC of 0.98 (0.95-1), P < 0.001, to detect HFpEF., Conclusions: Epi-GLS is a promising new imaging parameter to be considered in the clinical assessment of HFpEF patients. Given its excellent specificity, in tandem with a highly sensitive parameter such as NT-proBNP, Epi-GLS holds the potential to greatly improve the current diagnostic algorithms., (© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.)
- Published
- 2020
- Full Text
- View/download PDF
48. Variability of Myocardial Strain During Isometric Exercise in Subjects With and Without Heart Failure.
- Author
-
Blum M, Hashemi D, Motzkus LA, Neye M, Dordevic A, Zieschang V, Zamani SM, Lapinskas T, Runte K, Kelm M, Kühne T, Tahirovic E, Edelmann F, Pieske B, Düngen HD, and Kelle S
- Abstract
Background: Fast strain-encoded cardiac magnetic resonance imaging (cMRI, fast-SENC) is a novel technology potentially improving characterization of heart failure (HF) patients by quantifying cardiac strain. We sought to describe the impact of isometric handgrip exercise (HG) on cardiac strain assessed by fast-SENC in HF patients and controls. Methods: Patients with stable HF and controls were examined using cMRI at rest and during HG. Left ventricular (LV) global longitudinal strain (GLS) and global circumferential (GCS) were derived from image analysis software using fast-SENC. Strain change < -0.5 and > +0.5 was classified as increase and decrease, respectively. Results: The study population comprised 72 subjects, including HF with reduced, mid-range and preserved ejection fraction and controls (HFrEF n = 18 HFmrEF n = 18, HFpEF n = 17, controls: n = 19). In controls, LV GLS remained stable in 36.8%, increased in 36.8% and decreased in 26.3% of subjects during HG. In HF subgroups, similar patterns of LV GLS response were observed (HFpEF: stable 41.2%, increase 35.3%, decrease: 23.5%; HFmrEF: stable 50.0%, increase 16.7%, decrease: 33.3%; HFrEF: stable 33.3%, increase 22.2%, decrease: 44.4%, p = 0.668). Mean change between LV GLS at rest and during HG ranged close to zero with broad standard deviation in all subgroups and was not significantly different between subgroups (+1.2 ± 5.4%, -0.6 ± 8.3%, -1.7 ± 10.7%, and -3.1 ± 19.4%, p = 0.746 in controls, HFpEF, HFmrEF and HFrEF, respectively). However, the absolute value of LV GLS change-irrespective of increase or decrease-was significantly different between subgroups with 4.4 ± 3.2% in controls, 5.9 ± 5.7% in HFpEF, 6.8 ± 8.3% in HFmrEF and 14.1 ± 13.3% in HFrEF ( p = 0.005). The absolute value of LV GLS change significantly correlated with resting LVEF, NTproBNP and Minnesota Living with Heart Failure questionnaire scores. Conclusion: The response to isometric exercise in LV GLS is heterogeneous in all HF subgroups and in controls. The absolute value of LV GLS change during HG exercise is elevated in HF patients and associated with measures of HF severity. The diagnostic utility of fast-SENC strain assessment in conjunction with HG appears to be limited. Trial Registration: URL: https://www.drks.de; Unique Identifier: DRKS00015615., (Copyright © 2020 Blum, Hashemi, Motzkus, Neye, Dordevic, Zieschang, Zamani, Lapinskas, Runte, Kelm, Kühne, Tahirovic, Edelmann, Pieske, Düngen and Kelle.)
- Published
- 2020
- Full Text
- View/download PDF
49. Economic impact of heart failure with preserved ejection fraction: insights from the ALDO-DHF trial.
- Author
-
Hashemi D, Dettmann L, Trippel TD, Holzendorf V, Petutschnigg J, Wachter R, Hasenfuß G, Pieske B, Zapf A, and Edelmann F
- Subjects
- Aged, Austria, Female, Germany, Humans, Male, Mineralocorticoid Receptor Antagonists, Prospective Studies, Stroke Volume, Ventricular Function, Left, Heart Failure drug therapy
- Abstract
Aims: Although heart failure (HF) with preserved ejection fraction (HFpEF) is a leading cause for hospitalization, its overall costs remain unclear. Therefore, we assessed the health care-related costs of ambulatory HFpEF patients and the effect of spironolactone., Methods and Results: The aldosterone receptor blockade in diastolic HF trial is a multicentre, prospective, randomized, double-blind, placebo-controlled trial conducted between March 2007 and April 2011 at 10 sites in Germany and Austria that included 422 ambulatory patients [mean age: 67 years (standard deviation: 8); 52% women]. All subjects suffered from chronic New York Heart Association (NYHA) class II or III HF and preserved left ventricular ejection fraction of 50% or greater. They also showed evidence of diastolic dysfunction. Patients were randomly assigned to receive 25 mg of spironolactone once daily (n = 213) or matching placebo (n = 209) with 12 months of follow-up. We used a single-patient approach to explore the resulting general cost structure and included medication, number of general practitioner and cardiologist visits, and hospitalization in both acute and rehabilitative care facilities. The average annual costs per patient in this cohort came up to €1, 118 (±2,475), and the median costs were €332. We confirmed that the main cost factor was hospitalization and spironolactone did not affect the overall costs. We identified higher HF functional class (NYHA), male patients with low haemoglobin level, with high oxygen uptake (VO
2 max) and coronary artery disease, hyperlipidaemia, and atrial fibrillation as independent predictors for higher costs., Conclusions: In this relatively young, oligosymptomatic, and with regard to the protocol without major comorbidities patient cohort, the overall costs are lower than expected compared with the HFrEF population. Further investigation is needed to investigate the impact of, for example, comorbidities and their effect over a longer period of time. Simultaneously, this analysis suggests that prevention of comorbidities are necessary to reduce costs in the health care system., (© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.)- Published
- 2020
- Full Text
- View/download PDF
50. Syncopes and clinical outcome in heart failure: results from prospective clinical study data in Germany.
- Author
-
Hashemi D, Blum M, Mende M, Störk S, Angermann CE, Pankuweit S, Tahirovic E, Wachter R, Pieske B, Edelmann F, and Düngen HD
- Subjects
- Germany epidemiology, Humans, Male, Prospective Studies, Stroke Volume, Syncope, HIV Infections, Heart Failure complications, Heart Failure epidemiology
- Abstract
Aims: Whereas syncopal episodes are a frequent complication of cardiovascular disorders, including heart failure (HF), little is known whether syncopes impact the prognosis of patients with HF. We aimed to assess the impact of a history of syncope (HoS) on overall and hospitalization-free survival of these patients., Methods and Results: We pooled the data of prospective, nationwide, multicentre studies conducted within the framework of the German Competence Network for Heart Failure including 11 335 subjects. Excluding studies with follow-up periods <10 years, we assessed 5318 subjects. We excluded a study focusing on cardiac changes in patients with an HIV infection because of possible confounding factors and 849 patients due to either missing key parameters or missing follow-up data, resulting in 3594 eligible subjects, including 2130 patients with HF [1564 patients with heart failure with reduced ejection fraction (HFrEF), 314 patients with heart failure with mid-range ejection fraction, and 252 patients with heart failure with preserved ejection fraction (HFpEF)] and 1464 subjects without HF considered as controls. HoS was more frequent in the overall cohort of patients with HF compared with controls (P < 0.001)-mainly driven by the HFpEF subgroup (HFpEF vs. controls: 25.0% vs. 12.8%, P < 0.001). Of all the subjects, 14.6% reported a HoS. Patients with HFrEF in our pooled cohort showed more often syncopes than subjects without HF (15.0% vs. 12.8%, P = 0.082). Subjects with HoS showed worse overall survival [42.4% vs. 37.9%, hazard ratio (HR) = 1.21, 99% confidence interval (0.99, 1.46), P = 0.04] and less days alive out of hospital [HR = 1.39, 99% confidence interval (1.18, 1.64), P < 0.001] compared with all subjects without HoS. Patients with HFrEF with HoS died earlier [30.3% vs. 41.6%, HR = 1.40, 99% confidence interval (1.12, 1.74), P < 0.001] and lived fewer days out of hospital than those without HoS. We could not find these changes in mortality and hospital-free survival in the heart failure with mid-range ejection fraction and HFpEF cohorts. HoS represented a clinically high-risk profile within the HFrEF group-combining different risk factors. Further analyses showed that among patients with HFrEF with HoS, known cardiovascular risk factors (e.g. age, male sex, diabetes mellitus, and anaemia) were more prevalent. These constellations of the risk factors explained the effect of HoS in a multivariable Cox regression models., Conclusions: In a large cohort of patients with HF, HoS was found to be a clinically and easily accessible predictor of both overall and hospitalization-free survival in patients with HFrEF and should thus routinely be assessed., (© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Published
- 2020
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.