42 results on '"Akerud H"'
Search Results
2. Sexual orientation of women does not affect outcome of fertility treatment with donated sperm
- Author
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Nordqvist, S., Sydsjö, Gunilla, Lampic, C., Akerud, H., Elenis, E., Skoog Svanberg, A., Nordqvist, S., Sydsjö, Gunilla, Lampic, C., Akerud, H., Elenis, E., and Skoog Svanberg, A.
- Abstract
Is there a difference in fertility between heterosexual women and lesbians undergoing sperm donation? Women undergoing treatment with donated sperm are equally fertile regardless of sexual orientation. Lesbians have an increased prevalence of smoking, obesity, sexually transmitted diseases and, possibly, polycystic ovary syndrome, all factors known to affect fertility. Previous studies on sperm donation inseminations (D-IUI) show conflicting results regarding pregnancy outcome. This is a national study of 171 lesbians and 124 heterosexual women undergoing sperm donation both as D-IUI (lesbian n 438, heterosexual n 298) and as embryo transfers (ET) after IVF with donated sperm (lesbians n 225, heterosexuals n 230) during 20052010. All clinics in Sweden offering sperm donation recruited patients. Differences in patients medical history, treatment results and number of treatments to live birth were analyzed using independent samples t-test, Pearsons (2) test or Fishers exact probability test. 71.8 of heterosexuals and 69.0 of lesbians had a child after treatment. The mean number of treatments was 4.2 for heterosexual women and 3.9 for lesbians. The total live birth rate, regardless of treatment type, was 19.7 for heterosexuals and 19.5 for lesbians. For D-IUI, the live birth rate was 12.8 for heterosexuals and 16.0 for lesbians and the live birth rate for all IVF embryo transfers (fresh and thawed cycles) was 28.7 for heterosexuals and 26.2 for lesbians. There were no differences in live birth rate between the groups for each of the different types of insemination stimulations (natural cycle; clomiphene citrate; FSH; clomiphene citrate and FSH combined). Nor was there a difference in live birth rate between the groups for either fresh or thawed embryo transfer. There was no difference between the proportions of women in either group or the number of treatments needed to achieve a live birth. Heterosexuals had a higher prevalence of smokers (9.2), uterine polyps (7.2) o
- Published
- 2014
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3. Low serum allopregnanolone is associated with elevated depressive symptoms in late pregnancy
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Hellgren, C., Akerud, H., Skalkidou, A., Bäckström, Torbjörn, Poromaa, I. Sundstrom, Hellgren, C., Akerud, H., Skalkidou, A., Bäckström, Torbjörn, and Poromaa, I. Sundstrom
- Published
- 2012
4. Reproductive (epi)genetics
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Lynch, C., primary, Tee, N., additional, Rouse, H., additional, Gordon, A., additional, Sati, L., additional, Zeiss, C., additional, Soygur, B., additional, Bassorgun, I., additional, Goksu, E., additional, Demir, R., additional, McGrath, J., additional, Groendahl, M. L., additional, Thuesen, L., additional, Andersen, A. N., additional, Loft, A., additional, Smitz, J., additional, Adriaenssens, T., additional, Vikesa, J., additional, Borup, R., additional, Mersy, E., additional, Kisters, N., additional, Macville, M. V. E., additional, Engelen, J. J. M., additional, Consortium, S.-E. N. N., additional, Menheere, P. P. C. A., additional, Geraedts, J. P., additional, Coumans, A. B. C., additional, Frints, S. G. M., additional, Aledani, T., additional, Assou, S., additional, Traver, S., additional, Ait-ahmed, O., additional, Dechaud, H., additional, Hamamah, S., additional, Mizutani, E., additional, Suzumori, N., additional, Sugiyama, C., additional, Hattori, Y., additional, Sato, T., additional, Ando, H., additional, Ozaki, Y., additional, Sugiura-Ogasawara, M., additional, Wissing, M., additional, Kristensen, S. G., additional, Andersen, C. Y., additional, Mikkelsen, A. L., additional, Hoest, T., additional, Velthut-Meikas, A., additional, Simm, J., additional, Metsis, M., additional, Salumets, A., additional, Palini, S., additional, Galluzzi, L., additional, De Stefani, S., additional, Primiterra, M., additional, Wells, D., additional, Magnani, M., additional, Bulletti, C., additional, Vogt, P. H., additional, Frank-Herrmann, P., additional, Bender, U., additional, Strowitzki, T., additional, Besikoglu, B., additional, Heidemann, P., additional, Wunsch, L., additional, Bettendorf, M., additional, Jelinkova, L., additional, Vilimova, S., additional, Kosarova, M., additional, Sebek, P., additional, Volemanova, E., additional, Kruzelova, M., additional, Civisova, J., additional, Svobodova, L., additional, Sobotka, V., additional, Mardesic, T., additional, van de Werken, C., additional, Santos, M. A., additional, Eleveld, C., additional, Laven, J. S. E., additional, Baart, E. B., additional, Pylyp, L. Y., additional, Spinenko, L. A., additional, Zukin, V. D., additional, Perez-Sanz, J., additional, Matorras, R., additional, Arluzea, J., additional, Bilbao, J., additional, Gonzalez-Santiago, N., additional, Yeh, N., additional, Koff, A., additional, Barlas, A., additional, Romin, Y., additional, Manova-Todorova, K., additional, Hoz, C. D. l., additional, Mauri, A. L., additional, Nascimento, A. M., additional, Vagnini, L. D., additional, Petersen, C. G., additional, Ricci, J., additional, Massaro, F. C., additional, Cavagna, M., additional, Pontes, A., additional, Oliveira, J. B. A., additional, Baruffi, R. L. R., additional, Franco, J. G., additional, Wu, E. X., additional, Ma, S., additional, Parriego, M., additional, Sole, M., additional, Boada, M., additional, Coroleu, B., additional, Veiga, A., additional, Kakourou, G., additional, Poulou, M., additional, Vrettou, C., additional, Destouni, A., additional, Traeger-Synodinos, J., additional, Kanavakis, E., additional, Yatsenko, A. N., additional, Georgiadis, A. P., additional, McGuire, M. M., additional, Zorrilla, M., additional, Bunce, K. D., additional, Peters, D., additional, Rajkovic, A., additional, Olszewska, M., additional, Kurpisz, M., additional, Gilbertson, A. Z. A., additional, Ottolini, C. S., additional, Summers, M. C., additional, Sage, K., additional, Handyside, A. H., additional, Thornhill, A. R., additional, Griffin, D. K., additional, Chung, M. K., additional, Kim, J. W., additional, Lee, J. H., additional, Jeong, H. J., additional, Kim, M. H., additional, Ryu, M. J., additional, Park, S. J., additional, Kang, H. Y., additional, Lee, H. S., additional, Zimmermann, B., additional, Banjevic, M., additional, Hill, M., additional, Lacroute, P., additional, Dodd, M., additional, Sigurjonsson, S., additional, Lau, P., additional, Prosen, D., additional, Chopra, N., additional, Ryan, A., additional, Hall, M., additional, McAdoo, S., additional, Demko, Z., additional, Levy, B., additional, Rabinowitz, M., additional, Vereczeky, A., additional, Kosa, Z. S., additional, Savay, S., additional, Csenki, M., additional, Nanassy, L., additional, Dudas, B., additional, Domotor, Z. S., additional, Debreceni, D., additional, Rossi, A., additional, Alegretti, J. R., additional, Cuzzi, J., additional, Bonavita, M., additional, Tanada, M., additional, Matunaga, P., additional, Fettback, P., additional, Rosa, M. B., additional, Maia, V., additional, Hassun, P., additional, Motta, E. L. A., additional, Piccolomini, M., additional, Gomes, C., additional, Barros, B., additional, Nicoliello, M., additional, Criscuolo, T., additional, Miyadahira, E., additional, Montjean, D., additional, Benkhalifa, M., additional, Berthaut, I., additional, Griveau, J. F., additional, Morcel, K., additional, Bashamboo, A., additional, McElreavey, K., additional, Ravel, C., additional, Rubio, C., additional, Rodrigo, L., additional, Mateu, E., additional, Mercader, A., additional, Peinado, V., additional, Buendia, P., additional, Milan, M., additional, Delgado, A., additional, Al-Asmar, N., additional, Escrich, L., additional, Campos-Galindo, I., additional, Garcia-Herrero, S., additional, Poo, M. E., additional, Mir, P., additional, Simon, C., additional, Reyes-Engel, A., additional, Cortes-Rodriguez, M., additional, Lendinez, A., additional, Perez-Nevot, B., additional, Palomares, A. R., additional, Galdon, M. R., additional, Ruberti, A., additional, Minasi, M. G., additional, Biricik, A., additional, Colasante, A., additional, Zavaglia, D., additional, Iammarrone, E., additional, Fiorentino, F., additional, Greco, E., additional, Demir, N., additional, Ozturk, S., additional, Sozen, B., additional, Morales, R., additional, Lledo, B., additional, Ortiz, J. A., additional, Ten, J., additional, Llacer, J., additional, Bernabeu, R., additional, Nagayoshi, M., additional, Tanaka, A., additional, Tanaka, I., additional, Kusunoki, H., additional, Watanabe, S., additional, Temel, S. G., additional, Beyazyurek, C., additional, Ekmekci, G. C., additional, Aybar, F., additional, Cinar, C., additional, Kahraman, S., additional, Nordqvist, S., additional, Karehed, K., additional, Akerud, H., additional, Gultomruk, M., additional, Tulay, P., additional, Findikli, N., additional, Yagmur, E., additional, Karlikaya, G., additional, Ulug, U., additional, Bahceci, M., additional, Bargallo, M. F., additional, Arevalo, M. R., additional, Salat, M. M., additional, Barbat, I. V., additional, Lopez, J. T., additional, Algam, M. E., additional, Boluda, A. B., additional, de Oya, G. C., additional, Tolmacheva, E. N., additional, Kashevarova, A. A., additional, Skryabin, N. A., additional, Lebedev, I. N., additional, Semaco, E., additional, Belo, A., additional, Riboldi, M., additional, Luz, L., additional, Nobrega, N., additional, Mazetto, R., additional, Alegretti, J. A., additional, Bibancos, M., additional, Serafini, P., additional, Neupane, J., additional, Vandewoestyne, M., additional, Heindryckx, B., additional, Deroo, T., additional, Lu, Y., additional, Ghimire, S., additional, Lierman, S., additional, Qian, C., additional, Deforce, D., additional, De Sutter, P., additional, Viloria, T., additional, Martinez-Jabaloyas, J. M., additional, Gil-Salom, M., additional, Capalbo, A., additional, Treff, N., additional, Cimadomo, D., additional, Tao, X., additional, Ferry, K., additional, Ubaldi, F. M., additional, Rienzi, L., additional, Scott, R. T., additional, Katzorke, N., additional, Vogt, H. P., additional, Hehr, A., additional, Gassner, C., additional, Paulmann, B., additional, Kowalzyk, Z., additional, Klatt, M., additional, Krauss, S., additional, Seifert, D., additional, Seifert, B., additional, Hehr, U., additional, Lobascio, M., additional, Varricchio, M. T., additional, Rubino, P., additional, Bono, S., additional, Cotarelo, R. P., additional, Spizzichino, L., additional, Colicchia, A., additional, Giannini, P., additional, Suhorutshenko, M., additional, and Rosenstein-Tamm, K., additional
- Published
- 2013
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5. Embryology
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Gandhi, G., primary, Allahbadia, G., additional, Kagalwala, S., additional, Allahbadia, A., additional, Ramesh, S., additional, Patel, K., additional, Hinduja, R., additional, Chipkar, V., additional, Madne, M., additional, Ramani, R., additional, Joo, J. K., additional, Jeung, J. E., additional, Go, K. R., additional, Lee, K. S., additional, Goto, H., additional, Hashimoto, S., additional, Amo, A., additional, Yamochi, T., additional, Iwata, H., additional, Morimoto, Y., additional, Koifman, M., additional, Lahav-Baratz, S., additional, Blais, E., additional, Megnazi-Wiener, Z., additional, Ishai, D., additional, Auslender, R., additional, Dirnfeld, M., additional, Zaletova, V., additional, Zakharova, E., additional, Krivokharchenko, I., additional, Zaletov, S., additional, Zhu, L., additional, Li, Y., additional, Zhang, H., additional, Ai, J., additional, Jin, L., additional, Zhang, X., additional, Rajan, N., additional, Kovacs, A., additional, Foley, C., additional, Flanagan, J., additional, O'Callaghan, J., additional, Waterstone, J., additional, Dineen, T., additional, Dahdouh, E. M., additional, St-Michel, P., additional, Granger, L., additional, Carranza-Mamane, B., additional, Faruqi, F., additional, Kattygnarath, T. V., additional, Gomes, F. L. A. F., additional, Christoforidis, N., additional, Ioakimidou, C., additional, Papas, C., additional, Moisidou, M., additional, Chatziparasidou, A., additional, Klaver, M., additional, Tilleman, K., additional, De Sutter, P., additional, Lammers, J., additional, Freour, T., additional, Splingart, C., additional, Barriere, P., additional, Ikeno, T., additional, Nakajyo, Y., additional, Sato, Y., additional, Hirata, K., additional, Kyoya, T., additional, Kyono, K., additional, Campos, F. B., additional, Meseguer, M., additional, Nogales, M., additional, Martinez, E., additional, Ariza, M., additional, Agudo, D., additional, Rodrigo, L., additional, Garcia-Velasco, J. A., additional, Lopes, A. S., additional, Frederickx, V., additional, Vankerkhoven, G., additional, Serneels, A., additional, Roziers, P., additional, Puttermans, P., additional, Campo, R., additional, Gordts, S., additional, Fragouli, E., additional, Alfarawati, S., additional, Spath, K., additional, Wells, D., additional, Liss, J., additional, Lukaszuk, K., additional, Glowacka, J., additional, Bruszczynska, A., additional, Gallego, S. C., additional, Lopez, L. O., additional, Vila, E. O., additional, Garcia, M. G., additional, Canas, C. L., additional, Segovia, A. G., additional, Ponce, A. G., additional, Calonge, R. N., additional, Peregrin, P. C., additional, Ito, K., additional, Nakaoka, Y., additional, Alcoba, D. D., additional, Valerio, E. G., additional, Conzatti, M., additional, Tornquist, J., additional, Kussler, A. P., additional, Pimentel, A. M., additional, Corleta, H. E., additional, Brum, I. S., additional, Boyer, P., additional, Montjean, D., additional, Tourame, P., additional, Gervoise-Boyer, M., additional, Cohen, J., additional, Lefevre, B., additional, Radio, C. I., additional, Wolf, J. P., additional, Ziyyat, A., additional, De Croo, I., additional, Tolpe, A., additional, Degheselle, S., additional, Van de Velde, A., additional, Van den Abbeel, E., additional, Gandhi, G., additional, Kuwayama, M., additional, Khatoon, A., additional, Alsule, S., additional, Inaba, M., additional, Ohgaki, A., additional, Ohtani, A., additional, Matsumoto, H., additional, Mizuno, S., additional, Mori, R., additional, Fukuda, A., additional, Umekawa, Y., additional, Yoshida, A., additional, Tanigiwa, S., additional, Seida, K., additional, Suzuki, H., additional, Tanaka, M., additional, Vahabi, Z., additional, Yazdi, P. E., additional, Dalman, A., additional, Ebrahimi, B., additional, Mostafaei, F., additional, Niknam, M. R., additional, Watanabe, S., additional, Kamihata, M., additional, Tanaka, T., additional, Matsunaga, R., additional, Yamanaka, N., additional, Kani, C., additional, Ishikawa, T., additional, Wada, T., additional, Morita, H., additional, Miyamura, H., additional, Nishio, E., additional, Ito, M., additional, Kuwahata, A., additional, Ochi, M., additional, Horiuchi, T., additional, Dal Canto, M., additional, Guglielmo, M. C., additional, Fadini, R., additional, Renzini, M. M., additional, Albertini, D. F., additional, Novara, P., additional, Lain, M., additional, Brambillasca, F., additional, Turchi, D., additional, Sottocornola, M., additional, Coticchio, G., additional, Kato, M., additional, Fukunaga, N., additional, Nagai, R., additional, Kitasaka, H., additional, Yoshimura, T., additional, Tamura, F., additional, Hasegawa, N., additional, Nakayama, K., additional, Takeuchi, M., additional, Ohno, H., additional, Aoyagi, N., additional, Kojima, E., additional, Itoi, F., additional, Hashiba, Y., additional, Asada, Y., additional, Kikuchi, H., additional, Iwasa, Y., additional, Kamono, T., additional, Suzuki, A., additional, Yamada, K., additional, Kanno, H., additional, Sasaki, K., additional, Murakawa, H., additional, Matsubara, M., additional, Yoshida, H., additional, Valdespin, C., additional, Elhelaly, M., additional, Chen, P., additional, Pangestu, M., additional, Catt, S., additional, Hojnik, N., additional, Kovacic, B., additional, Roglic, P., additional, Taborin, M., additional, Zafosnik, M., additional, Knez, J., additional, Vlaisavljevic, V., additional, Mori, C., additional, Yabuuchi, A., additional, Ezoe, K., additional, Takayama, Y., additional, Aono, F., additional, Kato, K., additional, Radwan, P., additional, Krasinski, R., additional, Chorobik, K., additional, Radwan, M., additional, Stoppa, M., additional, Maggiulli, R., additional, Capalbo, A., additional, Ievoli, E., additional, Dovere, L., additional, Scarica, C., additional, Albricci, L., additional, Romano, S., additional, Sanges, F., additional, Barnocchi, N., additional, Papini, L., additional, Vivarelli, A., additional, Ubaldi, F. M., additional, Rienzi, L., additional, Bono, S., additional, Spizzichino, L., additional, Rubio, C., additional, Fiorentino, F., additional, Ferris, J., additional, Favetta, L. A., additional, MacLusky, N., additional, King, W. A., additional, Madani, T., additional, Jahangiri, N., additional, Aflatoonian, R., additional, Cater, E., additional, Hulme, D., additional, Berrisford, K., additional, Jenner, L., additional, Campbell, A., additional, Fishel, S., additional, Zhang, X. Y., additional, Yilmaz, A., additional, Hananel, H., additional, Ao, A., additional, Vutyavanich, T., additional, Piromlertamorn, W., additional, Saenganan, U., additional, Samchimchom, S., additional, Wirleitner, B., additional, Lejeune, B., additional, Zech, N. H., additional, Vanderzwalmen, P., additional, Albani, E., additional, Parini, V., additional, Smeraldi, A., additional, Menduni, F., additional, Antonacci, R., additional, Marras, A., additional, Levi, S., additional, Morreale, G., additional, Pisano, B., additional, Di Biase, A., additional, Di Rosa, A., additional, Setti, P. E. L., additional, Puard, V., additional, Cadoret, V., additional, Tranchant, T., additional, Gauthier, C., additional, Reiter, E., additional, Guerif, F., additional, Royere, D., additional, Yoon, S. Y., additional, Eum, J. H., additional, Park, E. A., additional, Kim, T. Y., additional, Yoon, T. K., additional, Lee, D. R., additional, Lee, W. S., additional, Cabal, A. C., additional, Vallejo, B., additional, Campos, P., additional, Sanchez, E., additional, Serrano, J., additional, Remohi, J., additional, Nagornyy, V., additional, Mazur, P., additional, Mykytenko, D., additional, Semeniuk, L., additional, Zukin, V., additional, Guilherme, P., additional, Madaschi, C., additional, Bonetti, T. C. S., additional, Fassolas, G., additional, Izzo, C. R., additional, Santos, M. J. D. L., additional, Beltran, D., additional, Garcia-Laez, V., additional, Escriba, M. J., additional, Grau, N., additional, Escrich, L., additional, Albert, C., additional, Zuzuarregui, J. L., additional, Pellicer, A., additional, LU, Y., additional, Nikiforaki, D., additional, Meerschaut, F. V., additional, Neupane, J., additional, De Vos, W. H., additional, Lierman, S., additional, Deroo, T., additional, Heindryckx, B., additional, Li, J., additional, Chen, X. Y., additional, Lin, G., additional, Huang, G. N., additional, Sun, Z. Y., additional, Zhong, Y., additional, Zhang, B., additional, Li, T., additional, Zhang, S. P., additional, Ye, H., additional, Han, S. B., additional, Liu, S. Y., additional, Zhou, J., additional, Lu, G. X., additional, Zhuang, G. L., additional, Muela, L., additional, Roldan, M., additional, Gadea, B., additional, Martinez, M., additional, Perez, I., additional, Munoz, M., additional, Castello, C., additional, Asensio, M., additional, Fernandez, P., additional, Farreras, A., additional, Rovira, S., additional, Capdevila, J. M., additional, Velilla, E., additional, Lopez-Teijon, M., additional, Kovacs, P., additional, Matyas, S. Z., additional, Forgacs, V., additional, Reichart, A., additional, Rarosi, F., additional, Bernard, A., additional, Torok, A., additional, Kaali, S. G., additional, Sajgo, A., additional, Pribenszky, C. S., additional, Sozen, B., additional, Ozturk, S., additional, Yaba-Ucar, A., additional, Demir, N., additional, Gelo, N., additional, Stanic, P., additional, Hlavati, V., additional, ogoric, S., additional, Pavicic-Baldani, D., additional, prem-Goldtajn, M., additional, Radakovic, B., additional, Kasum, M., additional, Strelec, M., additional, Canic, T., additional, imunic, V., additional, Vrcic, H., additional, Ajina, M., additional, Negra, D., additional, Ben-Ali, H., additional, Jallad, S., additional, Zidi, I., additional, Meddeb, S., additional, Bibi, M., additional, Khairi, H., additional, Saad, A., additional, Gamiz, P., additional, Viloria, T., additional, Lima, E. T., additional, Fernandez, M. P., additional, Prieto, J. A. A., additional, Varela, M. O., additional, Kassa, D., additional, Munoz, E. M., additional, Kani, K., additional, Nor-Ashikin, M. N. K., additional, Norhazlin, J. M. Y., additional, Norita, S., additional, Wan-Hafizah, W. J., additional, Mohd-Fazirul, M., additional, Razif, D., additional, Hoh, B. P., additional, Dale, S., additional, Woodhead, G., additional, Andronikou, S., additional, Francis, G., additional, Tailor, S., additional, Vourliotis, M., additional, Almeida, P. A., additional, Krivega, M., additional, Van de Velde, H., additional, Lee, R. K., additional, Hwu, Y. M., additional, Lu, C. H., additional, Li, S. H., additional, Vaiarelli, A., additional, Desgro, M., additional, Baggiani, A., additional, Zannoni, E., additional, Kermavner, L. B., additional, Klun, I. V., additional, Pinter, B., additional, Vrtacnik-Bokal, E., additional, De Paepe, C., additional, Cauffman, G., additional, Verheyen, G., additional, Stoop, D., additional, Liebaers, I., additional, Stecher, A., additional, Zintz, M., additional, Neyer, A., additional, Bach, M., additional, Baramsai, B., additional, Schwerda, D., additional, Wiener-Megnazi, Z., additional, Fridman, M., additional, Blais, I., additional, Akerud, H., additional, Lindgren, K., additional, Karehed, K., additional, Wanggren, K., additional, Hreinsson, J., additional, Freijomil, B., additional, Weiss, A., additional, Neril, R., additional, Geslevich, J., additional, Beck-Fruchter, R., additional, Lavee, M., additional, Golan, J., additional, Ermoshkin, A., additional, Shalev, E., additional, Shi, W., additional, Zhang, S., additional, Zhao, W., additional, Xue, X. I. A., additional, Wang, M. I. N., additional, Bai, H., additional, Shi, J., additional, Smith, H. L., additional, Shaw, L., additional, Kimber, S., additional, Brison, D., additional, Boumela, I., additional, Assou, S., additional, Haouzi, D., additional, Ahmed, O. A., additional, Dechaud, H., additional, Hamamah, S., additional, Dasiman, R., additional, Nor-Shahida, A. R., additional, Salina, O., additional, Gabriele, R. A. F., additional, Ben-Yosef, D., additional, Shwartz, T., additional, Cohen, T., additional, Carmon, A., additional, Raz, N. M., additional, Malcov, M., additional, Frumkin, T., additional, Almog, B., additional, Vagman, I., additional, Kapustiansky, R., additional, Reches, A., additional, Azem, F., additional, Amit, A., additional, Cetinkaya, M., additional, Pirkevi, C., additional, Yelke, H., additional, Kumtepe, Y., additional, Atayurt, Z., additional, Kahraman, S., additional, Risco, R., additional, Hebles, M., additional, Saa, A. M., additional, Vilches-Ferron, M. A., additional, Sanchez-Martin, P., additional, Lucena, E., additional, Lucena, M., additional, Heras, M. D. L., additional, Agirregoikoa, J. A., additional, Barrenetxea, G., additional, De Pablo, J. L., additional, Lehner, A., additional, Pribenszky, C., additional, Murber, A., additional, Rigo, J., additional, Urbancsek, J., additional, Fancsovits, P., additional, Bano, D. G., additional, Sanchez-Leon, A., additional, Marcos, J., additional, Molla, M., additional, Amorocho, B., additional, Nicolas, M., additional, Fernandez, L., additional, Landeras, J., additional, Adeniyi, O. A., additional, Ehbish, S. M., additional, Brison, D. R., additional, Egashira, A., additional, Murakami, M., additional, Nagafuchi, E., additional, Tanaka, K., additional, Tomohara, A., additional, Mine, C., additional, Otsubo, H., additional, Nakashima, A., additional, Otsuka, M., additional, Yoshioka, N., additional, Kuramoto, T., additional, Choi, D., additional, Yang, H., additional, Park, J. H., additional, Jung, J. H., additional, Hwang, H. G., additional, Lee, J. H., additional, Lee, J. E., additional, Kang, A. S., additional, Yoo, J. H., additional, Kwon, H. C., additional, Lee, S. J., additional, Bang, S., additional, Shin, H., additional, Lim, H. J., additional, Min, S. H., additional, Yeon, J. Y., additional, Koo, D. B., additional, Higo, S., additional, Ruvalcaba, L., additional, Kobayashi, M., additional, Takeuchi, T., additional, Miwa, A., additional, Nagai, Y., additional, Momma, Y., additional, Takahashi, K., additional, Chuko, M., additional, Nagai, A., additional, Otsuki, J., additional, Kim, S. G., additional, Kim, Y. Y., additional, Kim, H. J., additional, Park, I. H., additional, Sun, H. G., additional, Lee, K. H., additional, Song, H. J., additional, Costa-Borges, N., additional, Belles, M., additional, Herreros, J., additional, Teruel, J., additional, Ballesteros, A., additional, Calderon, G., additional, Vossaert, L., additional, Qian, C., additional, Lu, Y., additional, Parys, J. B., additional, Deforce, D., additional, Leybaert, L., additional, Surlan, L., additional, Otasevic, V., additional, Velickovic, K., additional, Golic, I., additional, Vucetic, M., additional, Stankovic, V., additional, Stojnic, J., additional, Radunovic, N., additional, Tulic, I., additional, Korac, B., additional, Korac, A., additional, Elias, R., additional, Neri, Q. V., additional, Fields, T., additional, Schlegel, P. N., additional, Rosenwaks, Z., additional, Palermo, G. D., additional, Gilson, A., additional, Piront, N., additional, Heens, B., additional, Vastersaegher, C., additional, Vansteenbrugge, A., additional, Pauwels, P. C. P., additional, Abdel-Raheem, M. F., additional, Abdel-Rahman, M. Y., additional, Abdel-Gaffar, H. M., additional, Sabry, M., additional, Kasem, H., additional, Rasheed, S. M., additional, Amin, M., additional, Abdelmonem, A., additional, Ait-Allah, A. S., additional, VerMilyea, M., additional, Anthony, J., additional, Bucci, J., additional, Croly, S., additional, Coutifaris, C., additional, Cimadomo, D., additional, Dusi, L., additional, Colamaria, S., additional, Baroni, E., additional, Giuliani, M., additional, Sapienza, F., additional, Buffo, L., additional, Zivi, E., additional, Aizenman, E., additional, Barash, D., additional, Gibson, D., additional, Shufaro, Y., additional, Perez, M., additional, Aguilar, J., additional, Taboas, E., additional, Ojeda, M., additional, Suarez, L., additional, Munoz, E., additional, Casciani, V., additional, Minasi, M. G., additional, Scarselli, F., additional, Terribile, M., additional, Zavaglia, D., additional, Colasante, A., additional, Franco, G., additional, Greco, E., additional, Hickman, C., additional, Cook, C., additional, Gwinnett, D., additional, Trew, G., additional, Carby, A., additional, Lavery, S., additional, Asgari, L., additional, Paouneskou, D., additional, Jayaprakasan, K., additional, Maalouf, W., additional, Campbell, B. K., additional, Rega, E., additional, Alteri, A., additional, Cotarelo, R. P., additional, Rubino, P., additional, Colicchia, A., additional, Giannini, P., additional, Devjak, R., additional, Papler, T. B., additional, Tacer, K. F., additional, Verdenik, I., additional, Iussig, B., additional, Gala, A., additional, Ferrieres, A., additional, Vincens, C., additional, Bringer-Deutsch, S., additional, Brunet, C., additional, Conaghan, J., additional, Tan, L., additional, Gvakharia, M., additional, Ivani, K., additional, Chen, A., additional, Pera, R. R., additional, Bowman, N., additional, Montgomery, S., additional, Best, L., additional, Duffy, S., additional, Hirata, R., additional, Aoi, Y., additional, Habara, T., additional, Hayashi, N., additional, Dinopoulou, V., additional, Partsinevelos, G. A., additional, Bletsa, R., additional, Mavrogianni, D., additional, Anagnostou, E., additional, Stefanidis, K., additional, Drakakis, P., additional, Loutradis, D., additional, Hernandez, J., additional, Leon, C. L., additional, Puopolo, M., additional, Palumbo, A., additional, Atig, F., additional, Kerkeni, A., additional, D'Ommar, G., additional, Herrera, A. K., additional, Lozano, L., additional, Majerfeld, M., additional, Ye, Z., additional, Zaninovic, N., additional, Clarke, R., additional, Bodine, R., additional, Nagorny, V., additional, Zabala, A., additional, Pessino, T., additional, Outeda, S., additional, Blanco, L., additional, Leocata, F., additional, Asch, R., additional, Rajikin, M. H., additional, Nuraliza, A. S., additional, Machac, S., additional, Hubinka, V., additional, Larman, M., additional, Koudelka, M., additional, Budak, T. P., additional, Membrado, O. O., additional, Martinez, E. S., additional, Wilson, P., additional, McClure, A., additional, Nargund, G., additional, Raso, D., additional, Insua, M. F., additional, Lotti, B., additional, Giordana, S., additional, Baldi, C., additional, Barattini, J., additional, Cogorno, M., additional, Peri, N. F., additional, Neuspiller, F., additional, Resta, S., additional, Filannino, A., additional, Maggi, E., additional, Cafueri, G., additional, Ferraretti, A. P., additional, Magli, M. C., additional, Gianaroli, L., additional, Sioga, A., additional, Oikonomou, Z., additional, Chatzimeletiou, K., additional, Oikonomou, L., additional, Kolibianakis, E., additional, Tarlatzis, B. C., additional, Sarkar, M. R., additional, Ray, D., additional, Bhattacharya, J., additional, Alises, J. M., additional, Gumbao, D., additional, Hickman, C. F. L., additional, Fiorentino, I., additional, Gualtieri, R., additional, Barbato, V., additional, Braun, S., additional, Mollo, V., additional, Netti, P., additional, Talevi, R., additional, Bayram, A., additional, Findikli, N., additional, Serdarogullari, M., additional, Sahin, O., additional, Ulug, U., additional, Tosun, S. B., additional, Bahceci, M., additional, Leon, A. S., additional, Cardoso, M. C. A., additional, Aguiar, A. P. S., additional, Sartorio, C., additional, Evangelista, A., additional, Gallo-Sa, P., additional, Erthal-Martins, M. C., additional, Mantikou, E., additional, Jonker, M. J., additional, de Jong, M., additional, Wong, K. M., additional, van Montfoort, A. P. A., additional, Breit, T. M., additional, Repping, S., additional, Mastenbroek, S., additional, Power, E., additional, Jordan, K., additional, Aksoy, T., additional, Gultomruk, M., additional, Aktan, A., additional, Goktas, C., additional, Petracco, R., additional, Okada, L., additional, Azambuja, R., additional, Badalotti, F., additional, Michelon, J., additional, Reig, V., additional, Kvitko, D., additional, Tagliani-Ribeiro, A., additional, Badalotti, M., additional, Petracco, A., additional, Aydin, B., additional, Cepni, I., additional, Rodriguez-Arnedo, D., additional, Ten, J., additional, Guerrero, J., additional, Ochando, I., additional, and Bernabeu, R., additional
- Published
- 2013
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6. O735 THE USE OF OXYTOCIN DURING LABOR
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Wiberg‐Itzel, E., primary, Nordstrom, L., additional, Pembe, A.B., additional, Wihlback, A.‐C., additional, Hoesli, I., additional, and Akerud, H., additional
- Published
- 2012
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7. O730 SKIN CONDUCTANCE ACTIVITY - A NEW PREDICTOR FOR ONSET OF LABOR?
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Wallstrom, T., primary, Akerud, H., additional, and Wiberg-Itzel, E., additional
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- 2012
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8. Evaluation of the Discrepancy Between pH and Lactate in Combined Fetal Scalp Blood Sampling
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Liljeström, L., primary, Wikström, A.K., additional, Hanson, U., additional, Akerud, H., additional, and Jonsson, M., additional
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- 2012
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9. Histidine-Rich Glycoprotein as an Early Biomarker of Preeclampsia
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Bolin, M., primary, Akerud, P., additional, Hansson, A., additional, and Akerud, H., additional
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- 2011
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10. P288 Dysfunctional labour and maternal morbidity
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Wiberg-Itzel, E., primary, Holmgren, M., additional, Hallstrom, P., additional, and Akerud, H., additional
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- 2009
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11. Angiopoietin-1/Angiopoietin-2 Ratio for Prediction of Preeclampsia
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Bolin, M., primary, Wiberg-Itzel, E., additional, Wikstrom, A.-K., additional, Goop, M., additional, Larsson, A., additional, Olovsson, M., additional, and Akerud, H., additional
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- 2009
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12. Sexual orientation of women does not affect outcome of fertility treatment with donated sperm.
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Nordqvist, S, Sydsjö, G, Lampic, C, Akerud, H, Elenis, E, Skoog Svanberg, A, and Åkerud, H
- Abstract
Study Question: Is there a difference in fertility between heterosexual women and lesbians undergoing sperm donation?Summary Answer: Women undergoing treatment with donated sperm are equally fertile regardless of sexual orientation.What Is Known Already: Lesbians have an increased prevalence of smoking, obesity, sexually transmitted diseases and, possibly, polycystic ovary syndrome, all factors known to affect fertility. Previous studies on sperm donation inseminations (D-IUI) show conflicting results regarding pregnancy outcome.Study Design, Size, Duration: This is a national study of 171 lesbians and 124 heterosexual women undergoing sperm donation both as D-IUI (lesbian n = 438, heterosexual n = 298) and as embryo transfers (ET) after IVF with donated sperm (lesbians n = 225, heterosexuals n = 230) during 2005-2010.Participants/materials, Setting, Methods: All clinics in Sweden offering sperm donation recruited patients. Differences in patients' medical history, treatment results and number of treatments to live birth were analyzed using independent samples t-test, Pearson's χ(2) test or Fisher's exact probability test.Main Results and the Role Of Chance: 71.8% of heterosexuals and 69.0% of lesbians had a child after treatment. The mean number of treatments was 4.2 for heterosexual women and 3.9 for lesbians. The total live birth rate, regardless of treatment type, was 19.7% for heterosexuals and 19.5% for lesbians. For D-IUI, the live birth rate was 12.8% for heterosexuals and 16.0% for lesbians and the live birth rate for all IVF embryo transfers (fresh and thawed cycles) was 28.7% for heterosexuals and 26.2% for lesbians. There were no differences in live birth rate between the groups for each of the different types of insemination stimulations (natural cycle; clomiphene citrate; FSH; clomiphene citrate and FSH combined). Nor was there a difference in live birth rate between the groups for either fresh or thawed embryo transfer. There was no difference between the proportions of women in either group or the number of treatments needed to achieve a live birth. Heterosexuals had a higher prevalence of smokers (9.2%), uterine polyps (7.2%) or previous children (11.3%) than lesbians (smokers 2.8%, P = 0.03; polyps 1.8%, P = 0.03; child 2.5%, P = 0.003).Limitations, Reasons For Caution: This study is limited to women living in stable relationships undergoing treatment with donated sperm in a clinical setting and may not apply to single women or those undergoing home inseminations.Wider Implications Of the Findings: These results may influence healthcare policy decisions as well as increase the quality of clinical care and medical knowledge of healthcare professionals. The data also have important implications for individuals regarding screening, infertility diagnostic procedures and treatment types offered to heterosexuals and lesbians seeking pregnancy through sperm donation.Study Funding/competing Interest(s): Funding was granted by the Stiftelsen Familjeplaneringsfonden i Uppsala; the Swedish Research Council for Health, Working Life and Welfare; and the Marianne and Marcus Wallenberg Foundation. The authors report no conflicts of interest. [ABSTRACT FROM AUTHOR]- Published
- 2014
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13. P.2.a.008 Low serum allopregnanolone is associated with elevated depressive symptoms in late pregnancy
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Hellgren, C., Åkerud, H., Skalkidou, A., Bäckström, T., and Poromaa, I. Sundström
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- 2012
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14. Outcome of deliveries in healthy but obese women: obesity and delivery outcome
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Kaplan-Sturk Rebecka, Åkerud Helena, Volgsten Helena, Hellström-Westas Lena, and Wiberg-Itzel Eva
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Obesity ,Fetal outcome ,Delivery outcome ,Medicine ,Biology (General) ,QH301-705.5 ,Science (General) ,Q1-390 - Abstract
Abstract Background Obesity among fertile women is a global problem. 25% of pregnant Swedish women are overweight at admission to the antenatal clinic and 12% of them are considered as obese. Previous studies have shown an increased risk of delivery complications with an elevated maternal BMI. The aim of this study was to evaluate delivery outcomes in relation to maternal BMI on admission to the antenatal clinic. A healthy group of 787 women with full-term pregnancies and spontaneous onset of labor were included in the study. Delivery outcome was assessed in relation to maternal BMI when attending the antenatal clinic. Results The results indicated that in deliveries where the maternal BMI was >30 a high frequency of abnormal CTG trace during the last 30 minutes of labor was shown. A blood sample for evaluation of risk of fetal hypoxia was performed in only eight percent of these deliveries. A spontaneous vaginal delivery without intervention was noted in 85.7%, and 12% of neonates were delivered with an adverse fetal outcome compared to 2.8% in the group with a maternal BMI Conclusion These results indicate an increased risk at delivery for healthy, but obese women in labor. Furthermore, the delivery management may not always be optimal in these deliveries.
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- 2013
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15. Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: A retrospective case control study
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Granfors Michaela, Karypidis Helena, Hosseini Frida, Skjöldebrand-Sparre Lottie, Stavreus-Evers Anneli, Bremme Katarina, Landgren Britth-Marie, Sundström-Poromaa Inger, Wikström Anna-Karin, and Åkerud Helena
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Phosphodiesterase 8B ,Recurrent miscarriage ,Single nucleotide polymorphism ,Thyroid ,Internal medicine ,RC31-1245 ,Genetics ,QH426-470 - Abstract
Abstract Background Recurrent miscarriage affects approximately 1% of all couples. There is a known relation between hypothyroidism and recurrent miscarriage. Phosphodiesterase 8B (PDE8B) is a regulator of cyclic adenosine monophosphate (cAMP) with important influence on human thyroid metabolism. Single nucleotide polymorphism (SNP) rs 4704397 in the PDE8B gene has been shown to be associated with variations in serum Thyroid Stimulating Hormone (TSH) and thyroxine (T4) levels. The aim of this study was to investigate whether there is an association between the SNP rs 4704397 in the PDE8B gene and recurrent miscarriage. Methods The study was designed as a retrospective case control study. 188 cases with recurrent miscarriage were included and compared with 391 controls who had delivered at least once and with no history of miscarriage or assisted reproduction. Results No difference between cases and controls concerning age was found. Bivariate associations between homozygous A/A (OR 1.57, 95% CI 0.98-2.52) as well as G/G carriers (OR 1.52, 95% CI 1.02-2.25) of SNP rs 4704397 in PDE8B and recurrent miscarriage were verified (test for trend across all 3 genotypes, p = 0.059). After adjustment for known confounders such as age, BMI and smoking the association between homozygous A/A (AOR 1.63, 95% CI 1.01 - 2.64, p = 0.045) and G/G (AOR 1.52, 95% CI 1.02 - 2.27, p = 0.039) carriers of SNP rs 4704397 in PDE8B and recurrent miscarriage remained. Conclusions Our findings suggest that there is an association between homozygous A/A as well as homozygous G/G carriers of SNP rs 4704397 in PDE8B and recurrent miscarriage.
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- 2012
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16. Loss-of-heterozygosity on chromosome 19q in early-stage serous ovarian cancer is associated with recurrent disease
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Skirnisdottir Ingiridur, Mayrhofer Markus, Rydåker Maria, Åkerud Helena, and Isaksson Anders
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Allele-specific copy number ,FFPE ,LOH ,Prognosis ,Serous ovarian cancer ,TAPS ,Early-stage ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Background Ovarian cancer is a heterogeneous disease and prognosis for apparently similar cases of ovarian cancer varies. Recurrence of the disease in early stage (FIGO-stages I-II) serous ovarian cancer results in survival that is comparable to those with recurrent advanced-stage disease. The aim of this study was to investigate if there are specific genomic aberrations that may explain recurrence and clinical outcome. Methods Fifty-one women with early stage serous ovarian cancer were included in the study. DNA was extracted from formalin fixed samples containing tumor cells from ovarian tumors. Tumor samples from thirty-seven patients were analysed for allele-specific copy numbers using OncoScan single nucleotide polymorphism arrays from Affymetrix and the bioinformatic tool Tumor Aberration Prediction Suite. Genomic gains, losses, and loss-of-heterozygosity that associated with recurrent disease were identified. Results The most significant differences (p Conclusions The results of our study indicate that presence of two aberrations in TP53 on 17p and LOH on 19q in early stage serous ovarian cancer is associated with recurrent disease. Further studies related to the findings of chromosomes 17 and 19 are needed to elucidate the molecular mechanism behind the recurring genomic aberrations and the poor clinical outcome.
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- 2012
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17. Different SNP combinations in the GCH1 gene and use of labor analgesia
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Sundström-Poromaa Inger, Nyberg Fred, Grönbladh Alfhild, Dabo Fatimah, and Åkerud Helena
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Pathology ,RB1-214 - Abstract
Abstract Background The aim of this study was to investigate if there is an association between different SNP combinations in the guanosine triphosphate cyclohydrolase (GCH1) gene and a number of pain behavior related outcomes during labor. A population-based sample of pregnant women (n = 814) was recruited at gestational week 18. A plasma sample was collected from each subject. Genotyping was performed and three single nucleotide polymorphisms (SNP) previously defined as a pain-protective SNP combination of GCH1 were used. Results Homozygous carriers of the pain-protective SNP combination of GCH1 arrived to the delivery ward with a more advanced stage of cervical dilation compared to heterozygous carriers and non-carriers. However, homozygous carriers more often used second line labor analgesia compared to the others. Conclusion The pain-protective SNP combination of GCH1 may be of importance in the limited number of homozygous carriers during the initial dilation of cervix but upon arrival at the delivery unit these women are more inclined to use second line labor analgesia.
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- 2010
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18. Hyperemesis gravidarum and risks of placental dysfunction disorders: a population-based cohort study.
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Bolin, M., Akerud, H., Cnattingius, S., Stephansson, O., and Wikström, A.K.
- Published
- 2013
19. Cell Cycle Regulator p27 Mediates Body Mass Index Effects in Ovarian Cancer in FIGO-stages I-II.
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Skirnisdottir I, Akerud H, Seidal T, and Sundstrom-Poromaa I
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- Adult, Disease-Free Survival, Female, Humans, Middle Aged, Neoplasm Staging, Ovarian Neoplasms pathology, Survival Rate, Body Mass Index, Cyclin-Dependent Kinase Inhibitor p27 metabolism, Ovarian Neoplasms metabolism, Ovarian Neoplasms mortality
- Abstract
Background/aim: The aim of the present study was to evaluate the association between body mass index (BMI), the biomarker p27, and the clinical factors in FIGO-stages I-II ovarian cancer., Patients and Methods: A total of 128 patients with ovarian cancer were included in the study. For testing differences in univariate analyzes we used the Pearson's Chi-square test and the log-rank test. For multivariate analyses the logistic regression and Cox regression models were used with recurrent disease and disease-free survival as endpoints, respectively., Results: Patients with BMI ≤25 kg/m
2 had a significantly better 5-year disease-free survival compared with patients with BMI >25 kg/m2 in the total series of patients (p=0.008), and in the series of patients (n=77) with non-serous tumors (p=0.047). Patients with p27-positive non-serous tumors had higher survival compared to patients with p27-negative non-serous tumors (p=0.020)., Conclusion: The cell cycle regulator p27 mediates BMI effects in ovarian cancer in FIGO-stages I-II., (Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)- Published
- 2019
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20. Induction of labor after one previous Cesarean section in women with an unfavorable cervix: A retrospective cohort study.
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Wallstrom T, Bjorklund J, Frykman J, Jarnbert-Pettersson H, Akerud H, Darj E, Gemzell-Danielsson K, and Wiberg-Itzel E
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- Adult, Cohort Studies, Female, Humans, Retrospective Studies, Cervix Uteri, Cesarean Section, Labor, Induced statistics & numerical data
- Abstract
Objective: Uterine rupture is a well-known but unusual complication in vaginal deliveries with a Cesarean section in the history. The risk of uterine rupture is at least two-fold when labor is induced. In Sweden, women are allowed to deliver vaginally after one previous Cesarean section, regardless if labor starts spontaneously or is induced. The aim of the study is to compare the proportion of uterine ruptures between the three methods (balloon catheter, Minprostin® and Cytotec®) for induction of labor in women with an unfavorable cervix and one previous Cesarean section., Material and Methods: Retrospective cohort study of all women with one previous Cesarean section and induction of labor with an unfavorable cervix at the four largest clinics in Stockholm during 2012-2015. Inclusion criteria: Women with a previous Cesarean section and induction of labor with a viable fetus, cephalic presentation, singleton, at ≥34 w, (n = 910)., Results: 3.0% (27/910) of the women with induction of labor had a uterine rupture, 91% of them had no previous vaginal delivery. The proportion of uterine ruptures was 2.0% (6/295) with orally administrated Cytotec®, 2.1% (7/335) with balloon catheter and 5.0% (14/ 281) when Minprostin® was used., Conclusions: No difference in the proportion of uterine ruptures was shown when orally administrated Cytotec® and balloon catheter were compared (p = 0.64). Orally administrated Cytotec® and balloon catheter give a high success rate of vaginal deliveries (almost 70%) despite an unfavorable cervix., Competing Interests: The authors declared that no competing interests exist.
- Published
- 2018
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21. Labor Induction with Orally Administrated Misoprostol: A Retrospective Cohort Study.
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Wallstrom T, Jarnbert-Pettersson H, Stenson D, Akerud H, Darj E, Gemzell-Danielsson K, and Wiberg-Itzel E
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- Administration, Oral, Adult, Cesarean Section, Female, Humans, Odds Ratio, Pregnancy, Pregnancy Outcome, Retrospective Studies, Risk Factors, Labor, Induced, Misoprostol administration & dosage, Misoprostol pharmacology
- Abstract
Introduction: One great challenge in obstetric care is labor inductions. Misoprostol has advantages in being cheap and stable at room temperature and available in resource-poor settings., Material and Methods: Retrospective cohort study of 4002 singleton pregnancies with a gestational age ≥34 w at Sodersjukhuset, Stockholm, during 2009-2010 and 2012-2013. Previously used methods of labor induction were compared with misoprostol given as a solution to drink, every second hour. Main outcome is as follows: Cesarean Section (CS) rate, acid-base status in cord blood, Apgar score < 7,5', active time of labor, and blood loss > 1500 ml (PPH)., Results: The proportion of CS decreased from 26% to 17% when orally given solution of misoprostol was introduced at the clinic ( p < 0.001). No significant difference in the frequency of low Apgar score ( p = 0.3), low aPh in cord blood ( p = 0.1), or PPH ( p = 0.4) between the different methods of induction was studied. After adjustment for different risk factor for CS the only method of induction which was associated with CS was dinoproston
⁎⁎ (Propess®) (aor = 2.9 (1.6-5.2))., Conclusion: Induction of labor with misoprostol, given as an oral solution to drink every second hour, gives a low rate of CS, without affecting maternal or fetal outcome.- Published
- 2017
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22. Induction of labor in women with a uterine scar.
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Stenson D, Wallstrom T, Sjostrand M, Akerud H, Gemzell-Danielsson K, and Wiberg-Itzel E
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- Administration, Oral, Adult, Female, Humans, Misoprostol administration & dosage, Oxytocics administration & dosage, Pregnancy, Retrospective Studies, Cesarean Section adverse effects, Labor, Induced adverse effects, Misoprostol adverse effects, Oxytocics adverse effects, Postoperative Complications etiology, Uterine Rupture etiology
- Abstract
Objective: To evaluate the frequency of uterine rupture following induction of labor in women with a previous cesarean section. Misoprostol was compared to other methods of induction., Methods: A retrospective cohort study of 208 women attempting induction of labor after one previous cesarean section. Delivery data were collected retrospectively and compared. Group 1(2009-2010) was compared with Group 2 (2012-2013). In Group 1, the main method of induction was vaginal PGE2 (prostaglandin-E2), amniotomy, oxytocin or a balloon catheter. In Group 2, the dominant method of induction was an oral solution of misoprostol., Main Outcome Measures: frequency of uterine rupture in the two groups., Results: Nine cases (4.3%) of uterine rupture occurred. There was no significant difference in the frequency of uterine rupture following the change of method of induction from PGE2, amniotomy, oxytocin or mechanical dilatation with a balloon catheter to orally administered misoprostol (4.1 versus 4.6%, p = 0.9). All ruptures occurred in women with no prior vaginal delivery., Conclusion: The shift to oral misoprostol as the primary method of induction in women with a previous cesarean section did not increase the frequency of uterine rupture in the cohort studied.
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- 2016
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23. Skin conductance activity in post-term pregnancies.
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Wallstrom T, Hellgren C, Akerud H, and Wiberg-Itzel E
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- Adult, Female, Humans, Logistic Models, Pregnancy, Prospective Studies, Galvanic Skin Response, Labor Onset physiology, Pain Threshold physiology, Pregnancy, Prolonged
- Abstract
Objective: The pain threshold in humans rises during late pregnancy, and the woman becomes less sensitive to stress. The aim of this study was to investigate whether monitoring the sympathetic nervous system response to stimuli by skin conductance activity might be a useful predictor of spontaneous onset of labour in post-term pregnancies., Study Design: A prospective observational study. Fifty-two healthy pregnant women were consecutively asked for inclusion in the study at their post-term pregnancy examination. Initially, a Ctg (cardiotocography) registration was performed, followed by 5 min of skin conductance measurement including a "cold pressor test". Finally, a vaginal examination with a cervical assessment were performed according to clinical guidelines., Results: A statistically significant lower pain reaction during the period of provocation was seen in deliveries close to spontaneous onset of labour compared with induced deliveries with an non-spontaneous onset of labour before 294 days (p = 0.02). Sixty-three per cent (19/30) of the women with spontaneous onset had a negative value at provocation compared with 30% (6/20) in the induced group., Conclusions: Decreased response to pain stimuli, as an indication of decreased activity in the sympathetic nervous system, has a correlation to spontaneous onset of labour in post-term pregnancies.
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- 2015
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24. Association between trefoil factor 3 gene variants and idiopathic recurrent spontaneous abortion.
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Haroun S, Altmäe S, Karypidis H, Kuningas M, Landgren BM, Akerud H, Skjöldebrand-Sparre L, Hosseini F, Bremme K, Sundström-Poromaa I, and Stavreus-Evers A
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- Endometrium metabolism, Female, Gene Frequency, Genetic Association Studies, Genotype, Haplotypes genetics, Humans, Peptides metabolism, Pregnancy, Sweden, Trefoil Factor-3, Abortion, Spontaneous genetics, Peptides genetics, Polymorphism, Single Nucleotide genetics
- Abstract
Trefoil factor 3 (TFF3) gene is an inflammatory mediator expressed in human endometrium during the window of implantation. The aim of this study was to evaluate the possible genetic association of TFF3 variants in recurrent spontaneous abortion. Women with a history of recurrent spontaneous abortion (n = 164) and healthy pregnant women (n = 143) were genotyped for five TFF3 polymorphisms (rs225439 G/A, rs533093 C/T, rs225361 A/G, rs11701143 T/C and rs77436142 G/C). In addition, haplotypes formed within the gene were analysed. Within the recurrent spontaneous abortion group, women who at some point had given birth and childless women had 4.19 ± 1.75 and 5.34 ± 3.42 consecutive spontaneous abortions, respectively. Women who had experience recurrent spontaneous abortions had a lower allele frequency of the rs11701143 promoter region minor C allele compared with fertile women (0.02 versus 0.05, P = 0.015). Patients with rs225361 AG genotype had significantly more successful pregnancies before spontaneous abortion than those with homozygous AA and GG genotypes (P = 0.014). No significant differences in haplotype frequencies between patients and controls were detected. Possible genetic risk factors identified that might contribute to the pathogenesis of idiopathic recurrent spontaneous abortion were TFF3 gene variants., (Copyright © 2014. Published by Elsevier Ltd.)
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- 2014
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25. Risk of placental dysfunction disorders after prior miscarriages: a population-based study.
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Gunnarsdottir J, Stephansson O, Cnattingius S, Akerud H, and Wikström AK
- Subjects
- Adult, Cohort Studies, Female, Fetal Growth Retardation etiology, Humans, Infant, Newborn, Infant, Small for Gestational Age, Logistic Models, Odds Ratio, Parity, Pre-Eclampsia etiology, Pregnancy, Premature Birth etiology, Registries, Risk Factors, Self Report, Stillbirth, Abortion, Spontaneous, Placenta Diseases etiology
- Abstract
Objective: The objective of the investigation was to study the association between prior miscarriages and the risks of placental dysfunction disorders, including preeclampsia, stillbirth, birth of a small for gestational age (SGA) infant, placental abruption, and spontaneous preterm birth., Study Design: In a population-based cohort study including 619,587 primiparous women, we estimated risks of placental dysfunction disorders for women with 1 (n = 68,185), 2 (n = 11,410) and 3 or more (n = 3823) self-reported prior miscarriages. Risks were calculated as odds ratios by unconditional logistic regression analysis and adjustments were made for maternal age, early pregnancy body mass index, height, smoking habits, country of birth, years of formal education, in vitro fertilization, chronic hypertension, pregestational diabetes, hypothyroidism, systemic lupus erythematosis, fetal sex, and year of childbirth., Results: Compared with women with no prior miscarriage, women with 1 prior miscarriage had almost no increased risks. Women with 2 prior miscarriages had increased risks of spontaneous preterm birth, preterm (<37 weeks) SGA infant, and placental abruption. The rates of all disorders were higher for women with 3 or more prior miscarriages compared with women without prior miscarriages: preeclampsia, 5.83% vs 4.27%; stillbirth, 0.69% vs 0.33%, SGA infant, 5.09% vs 3.22%, placental abruption, 0.81% vs 0.41%; and spontaneous preterm birth, 6.45% vs 4.40%. The adjusted odds ratios for preterm (<37 weeks) disorders in women with 3 prior miscarriages were approximately 2., Conclusion: History of 2 or more miscarriages is associated with an increased risk of placental dysfunction disorders and should be regarded as a risk factor in antenatal care., (Copyright © 2014 Mosby, Inc. All rights reserved.)
- Published
- 2014
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26. Experience of fetal scalp blood sampling during labor.
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Liljeström L, Wikström AK, Skalkidou A, Akerud H, and Jonsson M
- Subjects
- Adult, Blood Specimen Collection adverse effects, Female, Fetal Monitoring adverse effects, Humans, Hydrogen-Ion Concentration, Pain Measurement, Pregnancy, Scalp blood supply, Surveys and Questionnaires, Sweden, Blood Specimen Collection methods, Fetal Blood, Fetal Monitoring methods, Labor, Obstetric, Pain etiology
- Abstract
Fetal scalp blood sampling (FBS) is often claimed to be painful for women in labor and difficult for obstetricians to perform. Our aim was to assess women's experience of pain during FBS and obstetricians' experience of difficulty in performing the test. At a tertiary center in Sweden, a questionnaire with answers on a 10-point scale was completed by 51 women and the obstetricians performing the test. Women's experience of pain had a median of 3.5. FBS was well tolerated in women who had epidural analgesia but might be associated with pain in women without. Higher maternal body mass index and less cervical dilation were associated with higher pain ratings. Obstetricians did not generally experience scalp sampling as difficult to perform (median score 3.0). However, the sampling procedure can be more complicated in situations with higher maternal body mass index, less cervical dilation, and a higher station of the fetal head., (© 2013 Nordic Federation of Societies of Obstetrics and Gynecology.)
- Published
- 2014
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27. Napsin A as a marker of clear cell ovarian carcinoma.
- Author
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Skirnisdottir I, Bjersand K, Akerud H, and Seidal T
- Subjects
- Adenocarcinoma, Clear Cell metabolism, Adenocarcinoma, Clear Cell pathology, Adult, Aged, Aged, 80 and over, Aspartic Acid Endopeptidases metabolism, Cyclin-Dependent Kinase Inhibitor p21 metabolism, Cyclin-Dependent Kinase Inhibitor p27 metabolism, Female, Humans, Immunohistochemistry, Middle Aged, Neoplasm Grading, Neoplasm Staging, Ovarian Neoplasms metabolism, Ovarian Neoplasms pathology, ROC Curve, Tumor Suppressor Protein p53 metabolism, Adenocarcinoma, Clear Cell genetics, Aspartic Acid Endopeptidases genetics, Biomarkers, Tumor metabolism, Ovarian Neoplasms genetics
- Abstract
Background: Clear cell carcinomas are aggressive tumors with a distinct biologic behaviour. In a genome-wide screening for genes involved in chemo-resistance, NAPA was over-expressed in cisplatin-resistant cells. The NAPA (protein) Napsin A was described to promote resistance to cisplatin by degradation of the tumor suppressor p53., Methods: Totally 131 patients were included in this study all in FIGO-stages I-II; 16 were clear cell tumors which were compared with 40 Type I tumors and 75 type II tumors according to the markers Napsin A, p21, p53 and p27 and some clinical features. For detection of the markers tissue microarrays and immunohistochemistry were used., Results: Positivity for Napsin A was detected in 12 (80%) out of the 15 clear cell tumors available for analysis compared with 3 (4%) out of the Type I and II tumors in one group (p<0.001). Differences in p21 status, p53 status, and p21+p53- status were striking when clear cell tumors were compared with Type I, Type II, and Type I and II tumors in one group, respectively. The p21+p53-status was associated to positive staining of Napsin A (p=0.0015) and clear cell morphology (p=0.0003). In two separate multivariate logistic regression analyses with Napsin A as endpoint both clear cell carcinoma with OR=153 (95% C.I. 21-1107); (p<001) and p21+p53- status with OR=5.36 (95% C.I. 1.6-17.5); (p=0.005) were independent predictive factors. ROC curves showed that AUC for Napsin A alone was 0.882, for p21+p53- it was 0.720 and for p21+p53-Napsin A+AUC was 0.795. Patients with clear cell tumors had lower (p=0.013) BMI than Type I patients and were younger (p=0.046) at diagnosis than Type II patients. Clear cell tumors had a higher frequency (p=0.039) of capsule rupture at surgery than Type I and II tumors., Conclusions: Positivity of Napsin A in an epithelial ovarian tumor might strengthen the morphological diagnosis of clear cell ovarian carcinoma in the process of differential diagnosis between clear cell ovarian tumors and other histological subtypes.
- Published
- 2013
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28. Histidine-rich glycoprotein gene polymorphism in patients with recurrent miscarriage.
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Lindgren KE, Kårehed K, Karypidis H, Hosseini F, Bremme K, Landgren BM, Skjöldebrand-Sparre L, Stavreus-Evers A, Sundström-Poromaa I, and Akerud H
- Subjects
- Adult, Case-Control Studies, Female, Genotype, Heterozygote, Humans, Multivariate Analysis, Pregnancy, Thyroid Diseases epidemiology, Histidine-Rich Glycoprotein, Abortion, Habitual genetics, Polymorphism, Single Nucleotide, Proteins genetics
- Abstract
Association between the histidine-rich glycoprotein (HRG) C633T single nucleotide polymorphism (SNP) and recurrent miscarriage was investigated in a case-control study. The cases constituted 187 women with recurrent miscarriage that were compared with 395 controls who had delivered a child and had no history of miscarriage. Blood samples were collected from each woman, genomic DNA was extracted and genotyped for the HRG C633T SNP. In the whole study population, the percentage of miscarriage was the same, regardless of genotype (C/C 31.2%, C/T 32.9% and T/T 32.5%). However, an association between homozygous T/T carriers and recurrent miscarriage was detected in a subgroup of women with primary recurrent miscarriage (odds ratio 2.44, 95% CI 1.01-5.92). Our results indicate an important role for the HRG C633T SNP in the occurrence of recurrent miscarriage., (© 2013 Nordic Federation of Societies of Obstetrics and Gynecology.)
- Published
- 2013
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29. The effects of maternal depression and maternal selective serotonin reuptake inhibitor exposure on offspring.
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Olivier JD, Akerud H, Kaihola H, Pawluski JL, Skalkidou A, Högberg U, and Sundström-Poromaa I
- Abstract
It has been estimated that 20% of pregnant women suffer from depression and it is well-documented that maternal depression can have long-lasting effects on the child. Currently, common treatment for maternal depression has been the selective serotonin reuptake inhibitor medications (SSRIs) which are used by 2-3% of pregnant women in the Nordic countries and by up to 10% of pregnant women in the United States. Antidepressants cross the placenta and are transferred to the fetus, thus, the question arises as to whether children of women taking antidepressants are at risk for altered neurodevelopmental outcomes and, if so, whether the risks are due to SSRI medication exposure or to the underlying maternal depression. This review considers the effects of maternal depression and SSRI exposure on offspring development in both clinical and preclinical populations. As it is impossible in humans to study the effects of SSRIs without taking into account the possible underlying effects of maternal depression (healthy pregnant women do not take SSRIs), animal models are of great value. For example, rodents can be used to determine the effects of maternal depression and/or perinatal SSRI exposure on offspring outcomes. Unraveling the joint (or separate) effects of maternal depression and SSRI exposure will provide more insights into the risks or benefits of SSRI exposure during gestation and will help women make informed decisions about using SSRIs during pregnancy.
- Published
- 2013
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30. Sympathetic reactivity in late pregnancy is related to labour onset in women.
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Hellgren C, Akerud H, Jonsson M, and Sundström Poromaa I
- Subjects
- Adult, Cold Temperature, Cross-Sectional Studies, Female, Humans, Parturition, Galvanic Skin Response physiology, Labor Onset physiology, Pain Threshold physiology, Pregnancy physiology, Sympathetic Nervous System physiology
- Abstract
Stress regulation during pregnancy is considered to be connected to the timing of labour initiation. Although increasing knowledge is emerging on the regulation of parturition, there is currently no way to predict the start of spontaneous labour in women. The main aim of this study was to assess pain threshold and the sympathetic nervous system response to cold pain in relation to the onset of labour in healthy pregnant women. Ninety-three pregnant women were recruited and assessed for skin conductance (SC) activity during a cold pressor test in gestational week 38. Pain threshold and cold endurance were also measured and the results were compared with data obtained from hospital records. Seventy-four women had a spontaneous labour onset and a valid SC measurement. SC activity during the cold pressor test decreased significantly with the number of days left to spontaneous parturition. This may indicate a gradual decrease in sympathetic autonomic nervous system reactivity even during the last weeks of pregnancy. Measuring SC activity during mild stress provocation is a rapid and non-invasive means to study variation in sympathetic reactivity during pregnancy, and may be useful in research on stress regulation in pregnancy and its relation to labour initiation.
- Published
- 2011
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31. Evaluation of the discrepancy between pH and lactate in combined fetal scalp blood sampling.
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Liljeström L, Wikström AK, Hanson U, Akerud H, and Jonsson M
- Subjects
- Analysis of Variance, Cohort Studies, Female, Fetal Distress physiopathology, Gestational Age, Hospitals, University, Humans, Hydrogen-Ion Concentration, Labor, Obstetric, Lactates metabolism, Predictive Value of Tests, Pregnancy, Pregnancy Outcome, Risk Assessment, Scalp metabolism, Sensitivity and Specificity, Statistics, Nonparametric, Sweden, Fetal Blood chemistry, Fetal Monitoring methods, Lactates blood, Prenatal Care methods, Scalp blood supply
- Abstract
Objective: To evaluate the rate of discrepancy between pH and lactate values in fetal blood sampling (FBS). To evaluate differences in obstetric management in response to combined tests (pH and lactate) and single tests (pH or lactate)., Design: Descriptive study., Setting: Uppsala University Hospital, Sweden., Population: Labors monitored by FBS during one year (n=241)., Methods: Discrepancy in the combined tests was defined as a test having one abnormal and one normal value. Abnormal pH was defined as 7.24 or lower and abnormal lactate as 4.2 or higher. The results were categorized according to whether the test was normal or abnormal and according to whether it was a combined or single analysis., Main Outcome Measures: Discrepancy between pH and lactate values in combined tests. Frequency of operative delivery for fetal distress (ODFD). Time interval from the last FBS to ODFD., Results: In the combined tests with abnormality, a discrepancy between pH and lactate values occurred in 55%. The mean time interval from the last FBS to ODFD was longer in combined tests with one abnormal compared with two abnormal test results, 75 vs. 37 minutes (p<0.05). Operative delivery for fetal distress was performed less often after combined tests than after single tests: 41/62 (66%) vs. 19/20 (95%) (p<0.05)., Conclusion: In the combined test, discrepancies were common and occurred in half of the samples with an abnormality. Obstetric management was influenced by the discrepancy between test results with respect to ODFD rates and the time interval from the last FBS to delivery., (© 2011 The Authors Acta Obstetricia et Gynecologica Scandinavica© 2011 Nordic Federation of Societies of Obstetrics and Gynecology.)
- Published
- 2011
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32. Assessment of pain in women randomly allocated to speculum or digital insertion of the Foley catheter for induction of labor.
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Jonsson M, Hellgren C, Wiberg-Itzel E, and Akerud H
- Subjects
- Adult, Female, Humans, Labor, Induced methods, Pain Measurement, Patient Satisfaction, Pregnancy, Pregnancy Outcome, Surveys and Questionnaires, Cervical Ripening, Labor, Induced adverse effects, Pain etiology
- Abstract
Objective: The primary aim was to assess pain subjectively and objectively in women during insertion of a Foley catheter for induction of labor. A secondary aim was to assess pain during cervical ripening and to evaluate maternal satisfaction., Design: Randomized controlled trial., Setting: University hospital, Sweden., Population: Forty-two women undergoing induction of labor and cervical ripening with a Foley catheter., Methods: Women were randomly allocated to digital (n=21) or to speculum (n=21) placement of a Foley catheter. A visual analogue scale (VAS) was used for subjective assessment of pain and, for objective measurements, a skin conductance algesimeter was used and the area under the curve (AUC) was calculated (μSs). Maternal satisfaction was evaluated in a questionnaire., Main Outcome Measures: Pain sensation during placement of the Foley catheter., Results: There was a significant difference between groups in pain measurements during insertion of the Foley catheter. The speculum group had higher median pain scores than the digital group, VAS=5 vs. = 3 (p=0.03) and greater median AUC measurements: 1840 vs. 823 μSs (p=0.04). There was no difference in pain assessments during cervical ripening. Overall satisfaction scores were high and comparable between groups., Conclusion: Digital placement of the Foley catheter is subjectively and objectively less painful compared to the use of a speculum. Digital placement should therefore be considered as an alternative in the management of these patients. Ripening of the cervix with the Foley catheter is well tolerated and the overall satisfaction rate among patients induced with this method is high., (© 2011 The Authors Acta Obstetricia et Gynecologica Scandinavica© 2011 Nordic Federation of Societies of Obstetrics and Gynecology.)
- Published
- 2011
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33. Histidine-rich glycoprotein polymorphism and pregnancy outcome: a pilot study.
- Author
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Nordqvist S, Kårehed K, Stavreus-Evers A, and Akerud H
- Subjects
- Female, Fertilization in Vitro, Gene Frequency, Genotype, Homozygote, Humans, Infertility therapy, Pilot Projects, Polymorphism, Single Nucleotide, Pregnancy, Proteins physiology, Regression Analysis, Histidine-Rich Glycoprotein, Infertility genetics, Polymorphism, Genetic, Pregnancy Outcome genetics, Proteins genetics
- Abstract
Histidine-rich glycoprotein (HRG) is involved in fibrinolysis and coagulation, the immune system and angiogenesis. These processes are all crucial in establishing and maintaining pregnancy. The primary aim of this pilot study was to determine if HRG affects pregnancy outcome. The secondary aim was to investigate if a specific genetic polymorphism (rs9898 C/T) in the HRG gene is associated with pregnancy results. The polymorphism leads to expression of either a serine or proline residue at position 186 in the protein sequence. In this study, women undergoing IVF were included. The genetic polymorphism in the HRG gene was analysed by Western blot and single nucleotide polymorphism analysis. None of the women homozygous for the serine at residue 186 became pregnant whereas the women homozygous for proline at residue 186 had higher than expected pregnancy rates. As far as is known,this is the first study to show that a specific genetic polymorphism in the HRG gene of a woman affects her chances of becoming pregnant after IVF. The results may be essential in improving advice and IVF treatment for couples with unexplained infertility., (Copyright © 2011 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2011
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34. Association between adverse neonatal outcome and lactate concentration in amniotic fluid.
- Author
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Wiberg-Itzel E, Akerud H, Andolf E, Hellström-Westas L, Winbladh B, and Wennerholm UB
- Subjects
- Adult, Apgar Score, Bradycardia epidemiology, Cardiotocography, Female, Humans, Labor, Obstetric metabolism, Logistic Models, Pregnancy, Young Adult, Amniotic Fluid metabolism, Labor, Obstetric physiology, Lactates metabolism, Pregnancy Outcome
- Abstract
Objective: To estimate whether a high lactate concentration in amniotic fluid, together with cardiotocography, can be used as an indicator for an increased risk of adverse neonatal outcome at delivery., Method: A prospective cohort study was performed at two tertiary center labor wards in Sweden. Healthy women with full-term, singleton pregnancies and cephalic presentation in spontaneous active labor were included in the study (N=825). Lactate concentration in samples of amniotic fluid collected in the course of vaginal examinations during labor were correlated with cardiotocography 30 minutes before delivery and a composite score for adverse neonatal outcome., Results: High lactate concentration in amniotic fluid (greater than 10.1 mmol/L) was associated with an adverse neonatal outcome (odds ratio [OR] 4.4, 95% confidence interval [CI] 2.3-8.2). Fetal bradycardia within 30 minutes before delivery was also associated with an increased risk of adverse neonatal outcome (OR 7.4, 95% CI 3.04-18.11). If lactate in amniotic fluid was greater than 10.1 mmol/L and bradycardia was seen together, the risk of delivering a neonate with an adverse neonatal outcome was increased 11-fold (OR 10.7, 95% CI 3.7-31.7)., Conclusion: High lactate concentration in amniotic fluid and fetal bradycardia during the last 30 minutes before delivery indicate an increased risk of adverse neonatal outcome at delivery.
- Published
- 2011
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35. The presence of histidine-rich glycoprotein in the female reproductive tract and in embryos.
- Author
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Nordqvist S, Kårehed K, Hambiliki F, Wånggren K, Stavreus-Evers A, and Akerud H
- Subjects
- Biopsy, Female, Follicular Fluid metabolism, Humans, Immunohistochemistry, Pregnancy, Proteins genetics, RNA chemistry, RNA genetics, Reverse Transcriptase Polymerase Chain Reaction, Histidine-Rich Glycoprotein, Blastocyst metabolism, Embryonic Development physiology, Genitalia, Female metabolism, Placenta metabolism, Proteins metabolism
- Abstract
A well-regulated angiogenesis is crucial for proper embryo implantation, embryogenesis, and pregnancy development. Monitoring the presence and distribution of angiogenic regulators in the female reproductive tract and in the early embryo is important for a broader understanding of the molecular aspects of fertility, embryogenesis, and pregnancy. Histidine-rich glycoprotein (HRG) is a glycoprotein involved in angiogenesis. Its presence in the female reproductive tract or in embryos has not previously been studied. Follicular fluid, culture medium, and embryos were obtained from patients undergoing in vitro fertilization (IVF). Biopsies from inner genitalia and placenta were collected at surgery. Histidine-rich glycoprotein presence was investigated by immunohistochemistry and Western blot. Polymerase chain reaction (PCR) was used to determine HRG expression in tissues or by embryos. We identified HRG in follicular fluid, the female reproductive tract, and placenta, as well as in the embryos. Moreover, HRG expression was observed in blastocysts. Thus, the angiogenic properties of HRG might affect fertility.
- Published
- 2010
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36. Lactate concentration in amniotic fluid: a good predictor of labor outcome.
- Author
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Wiberg-Itzel E, Pettersson H, Andolf E, Hansson A, Winbladh B, and Akerud H
- Subjects
- Adult, Dystocia diagnosis, Female, Humans, Male, Pregnancy, Prospective Studies, Amniotic Fluid chemistry, Delivery, Obstetric, Labor, Obstetric, Lactic Acid analysis
- Abstract
Objective: Previous publications have suggested that high levels of lactate in amniotic fluid (AF) correlate with dysfunctional labor. The aim of this study was to investigate whether lactate concentration in AF together with the partogram is a better predictor of operative intervention in dysfunctional labor than the partogram alone., Study Design: A prospective observational study was carried out of 825 laboring women. Samples of AF were collected and the lactate concentration was analyzed at the bedside during labor. The main outcome of the study was the method of delivery (operative/spontaneous vaginal) in relation to the concentration of lactate in AF. Logistic regression was used to estimate the association between lactate concentration in AF and labor outcome and to adjust for well-known risk factors for dysfunctional labor., Results: 385/825 women had an arrested labor according to the partogram, and 193 of them were delivered operatively. High lactate in AF (>10.1 mmol/l) when labor arrested was associated with an increased risk of operative intervention due to dysfunctional labor (adjusted OR, 5.4, 95% CI, 3.2-9.1). Low levels of lactate in AF (<10.1 mmol/l) were associated with an increased probability of spontaneous vaginal delivery (adjusted OR, 2.7, 95% CI, 1.7-4.8)., Conclusion: The partogram together with the concentration of lactate in AF is a better predictor of operative intervention in dysfunctional labor than the partogram alone., (Copyright 2010 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2010
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37. Plasma levels of beta-endorphin during pregnancy and use of labor analgesia.
- Author
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Dabo F, Nyberg F, Qin Zhou, Sundström-Poromaa I, and Akerud H
- Subjects
- Adult, Analgesics therapeutic use, Cohort Studies, Female, Humans, Labor Pain drug therapy, Labor Pain therapy, Labor, Obstetric, Longitudinal Studies, Pregnancy Trimesters blood, Analgesia, Obstetrical statistics & numerical data, Pregnancy blood, beta-Endorphin blood
- Abstract
Beta-endorphins are endogenous opioid substances produced by the pituitary gland and placenta. The aims of this project were to longitudinally follow plasma levels of beta-endorphin during pregnancy in women with a healthy pregnancy and to investigate whether plasma levels of beta-endorphin in late pregnancy are associated with need for additional pain medication beyond nitrous oxide during labor. Plasma samples from 45 women were collected at gestational weeks 10, 25, 28, 33 and 37, and beta-endorphin was analyzed by radioimmunoassay (RIA). Plasma levels of beta-endorphin displayed a significant decrease in gestational weeks 28 and 33 compared to week 10, followed by a subsequent increase between gestational weeks 28 and 37. However, there was no change in levels of beta-endorphin between gestational weeks 10 and 37. Low levels of beta-endorphin at the end of pregnancy were associated with need for additional pain medication beyond nitrous oxide during labor, although the causal relationship is unclear.
- Published
- 2010
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38. Fibrinogen and histidine-rich glycoprotein in early-onset preeclampsia.
- Author
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Kårehed K, Wikström AK, Olsson AK, Larsson A, Olovsson M, and Akerud H
- Subjects
- Adult, Blood Coagulation physiology, Endothelial Cells metabolism, Female, Gestational Age, Humans, Immunohistochemistry, Pre-Eclampsia physiopathology, Pregnancy, Pregnancy Outcome, Tissue Distribution, Histidine-Rich Glycoprotein, Biomarkers, Tumor blood, Fibrinogen analysis, Placenta metabolism, Pre-Eclampsia blood, Proteins analysis
- Abstract
Objective: To determine whether plasma levels of fibrinogen and the placental tissue distributions of fibrinogen and histidine-rich glycoprotein (HRG) differ between early- and late-onset preeclampsia., Design: The study comprised 18 women with early-onset (gestational weeks 24-32) and 19 women with late-onset (gestational weeks 35-42) preeclampsia. As controls concerning the plasma levels of fibrinogen, we used samples from non-pregnant fertile women, healthy pregnant women at gestational weeks 24-32 and healthy pregnant women at gestational weeks 35-42. Placental samples from women with healthy pregnancies at gestational weeks 35-42 served as controls in the immunohistochemical staining., Setting: Uppsala University Hospital, Uppsala., Methods: Plasma fibrinogen levels were analyzed and the placental tissue expression of fibrinogen and HRG determined by immunohistochemistry., Results: Plasma level of fibrinogen was increased in early-onset, but not late-onset, preeclampsia. Levels of fibrinogen were significantly lower, and that of HRG significantly higher, in placentas from women with early-onset preeclampsia as compared with control placentas (p = 0.01 and 0.001)., Conclusions: HRG and fibrinogen might be involved in the hypercoagulability and the angiogenic imbalance seen in early-onset preeclampsia.
- Published
- 2010
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39. Lactate distribution in culture medium of human myometrial biopsies incubated under different conditions.
- Author
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Akerud H, Ronquist G, and Wiberg-Itzel E
- Subjects
- Aerobiosis, Anaerobiosis, Biopsy, Female, Humans, Immunohistochemistry, Monocarboxylic Acid Transporters metabolism, Muscle Proteins metabolism, Myometrium cytology, Pregnancy, Statistics, Nonparametric, Symporters metabolism, Lactates metabolism, Myometrium metabolism
- Abstract
It is generally believed that a relationship exists between muscle fatigue and intracellular accumulation of lactate. This reasoning is relevant to obstetrical issues. Myocytes in uterus work together during labor, and the contractions need to be strong and synchronized for a child to be delivered. At labor dystocia, the progress of labor becomes slow or arrested after a normal beginning. It has been described that, during labor dystocia, when the force of the contractions is low, the uterus is under hypoxia, and anaerobic conditions with high levels of lactate in amniotic fluid dominate. The purpose of this study was to examine whether myometrial cells are involved in the production of lactate in amniotic fluid and whether there are differences in production and distribution of lactate in cells incubated under aerobic and anaerobic conditions. We also wanted to elucidate the involvement of specific membrane-bound lactate carriers. Women undergoing elective caesarean section were included. Myometrial biopsies from uteri were collected and subjected to either immunohistochemistry to identify lactate carriers or in vitro experiments to analyze production of lactate. The presence of lactate carriers named monocarboxylate transporters 1 and 4 was verified. Myometrial cells produced lactate extracellularly, and the lactate carriers operated differently under anaerobic and aerobic conditions; while being mainly unidirectional under anaerobic conditions, they became bidirectional under aerobic conditions. Human myometrial cells produced and delivered lactate to the extracellular medium under both anaerobic and aerobic conditions. The delivery was mediated by lactate carriers.
- Published
- 2009
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40. Activated platelets provide a functional microenvironment for the antiangiogenic fragment of histidine-rich glycoprotein.
- Author
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Thulin A, Ringvall M, Dimberg A, Kårehed K, Väisänen T, Väisänen MR, Hamad O, Wang J, Bjerkvig R, Nilsson B, Pihlajaniemi T, Akerud H, Pietras K, Jahnen-Dechent W, Siegbahn A, and Olsson AK
- Subjects
- Amino Acid Sequence, Angiogenesis Inhibitors metabolism, Animals, Endothelial Cells metabolism, Female, Humans, Immunohistochemistry, Male, Mice, Mice, Inbred C57BL, Mice, Transgenic, Molecular Sequence Data, Neoplasms blood, Neovascularization, Pathologic blood, Neovascularization, Pathologic pathology, Peptide Fragments blood, Peptide Fragments metabolism, Platelet Activation, Repetitive Sequences, Amino Acid, Histidine-Rich Glycoprotein, Blood Platelets metabolism, Neoplasms blood supply, Neoplasms metabolism, Proteins metabolism
- Abstract
The angiogenesis inhibitor histidine-rich glycoprotein (HRG) constitutes one of several examples of molecules regulating both angiogenesis and hemostasis. The antiangiogenic properties of HRG are mediated via its proteolytically released histidine- and proline-rich (His/Pro-rich) domain. Using a combination of immunohistochemistry and mass spectrometry, we here provide biochemical evidence for the presence of a proteolytic peptide, corresponding to the antiangiogenic domain of HRG, in vivo in human tissue. This finding supports a role for HRG as an endogenous regulator of angiogenesis. Interestingly, the His/Pro-rich peptide bound to the vessel wall in tissue from cancer patients but not to the vasculature in tissue from healthy persons. Moreover, the His/Pro-rich peptide was found in close association with platelets. Relesate from in vitro-activated platelets promoted binding of the His/Pro-rich domain of HRG to endothelial cells, an effect mediated by Zn(2+). Previous studies have shown that zinc-dependent binding of the His/Pro-rich domain of HRG to heparan sulfate on endothelial cells is required for inhibition of angiogenesis. We describe a novel mechanism to increase the local concentration and activity of an angiogenesis inhibitor, which may reflect a host response to counteract angiogenesis during pathologic conditions. Our finding that tumor angiogenesis is elevated in HRG-deficient mice supports this conclusion.
- Published
- 2009
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41. Increased circulating levels of the antiangiogenic factor endostatin in early-onset but not late-onset preeclampsia.
- Author
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Wikström AK, Larsson A, Akerud H, and Olovsson M
- Subjects
- Adult, Angiogenesis Inhibitors biosynthesis, Biomarkers blood, Endostatins biosynthesis, Female, Humans, Pre-Eclampsia diagnosis, Pregnancy, Time Factors, Angiogenesis Inhibitors blood, Endostatins blood, Pre-Eclampsia blood
- Abstract
Changes in circulating angiogenic factors seem to play a key role in the pathogenesis of preeclampsia and it seems as if these changes are of greater importance in the pathogenesis of early-onset than of late-onset disease. Endostatin is a potent, broad spectrum antagonist of angiogenesis whose role in preeclampsia is poorly investigated. The aim of this study was to estimate whether circulating endostatin levels are altered in preeclampsia, and whether women with early-onset (before 32 weeks of gestation; n = 16) and late-onset (after 35 weeks of gestation; n = 19) preeclampsia differ in this regard. Women with early-onset, but not of late-onset preeclampsia had higher levels of endostatin than healthy pregnant women in corresponding lengths of gestation. The results of the study support the hypothesis that there is heterogeneity between early- and late-onset preeclampsia, with a stronger association between an altered angiogenic balance and early-onset than late-onset disease.
- Published
- 2009
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42. The minimal active domain of endostatin is a heparin-binding motif that mediates inhibition of tumor vascularization.
- Author
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Olsson AK, Johansson I, Akerud H, Einarsson B, Christofferson R, Sasaki T, Timpl R, and Claesson-Welsh L
- Subjects
- Amino Acid Sequence, Animals, Binding Sites, Cattle, Chemotaxis drug effects, Chick Embryo, Chorioallantoic Membrane blood supply, Endostatins genetics, Endostatins metabolism, Endothelium, Vascular cytology, Endothelium, Vascular drug effects, Female, Fibroblast Growth Factor 2 antagonists & inhibitors, Fibroblast Growth Factor 2 pharmacology, Humans, Mice, Mice, Inbred C57BL, Mice, SCID, Molecular Sequence Data, Neovascularization, Pathologic drug therapy, Neovascularization, Pathologic metabolism, Neovascularization, Physiologic, Peptide Fragments pharmacology, Protein Structure, Tertiary, Vascular Endothelial Growth Factor A antagonists & inhibitors, Vascular Endothelial Growth Factor A pharmacology, Endostatins pharmacology, Fibrosarcoma blood supply, Heparin metabolism, Pancreatic Neoplasms blood supply
- Abstract
Endostatin constitutes the COOH-terminal 20,000 Da proteolytic fragment of collagen XVIII and has been shown to possess antiangiogenic and antitumorigenic properties. In the present study, we have investigated the role of the heparin-binding sites in the in vivo mechanism of action of endostatin. The majority of the heparin binding is mediated by arginines 155/158/184/270 in endostatin, but there is also a minor site constituted by arginines 193/194. Using endostatin mutants lacking either of these two sites, we show that inhibition of fibroblast growth factor-2-induced angiogenesis in the chicken chorioallantoic membrane requires both heparin-binding sites. In contrast, inhibition of vascular endothelial growth factor-A-induced chorioallantoic membrane angiogenesis by endostatin was only dependent on the minor heparin-binding site (R193/194). These arginines were also required for endostatin to inhibit fibroblast growth factor-2- and vascular endothelial growth factor-A-induced chemotaxis of primary endothelial cells. Moreover, we show that a synthetic peptide corresponding to amino acids 180-199 of human endostatin (which covers the minor heparin-binding site) inhibits endothelial cell chemotaxis and reduces tumor vascularization in vivo. Substitution of arginine residues 193/194 for alanine attenuates the antiangiogenic effects of the peptide. These data show an essential role for heparin binding in the antiangiogenic action of endostatin.
- Published
- 2004
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