Author: "Ligthart, S. (Symen)" - Searchworks@Jio Institute Digital Library Search Results

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22 results on '"Ligthart, S. (Symen)"'

1. Genetic analysis of over half a million people characterises C-reactive protein loci

Author: Said, S. (Saredo), Pazoki, R. (Raha), Karhunen, V. (Ville), Võsa, U. (Urmo), Ligthart, S. (Symen), Bodinier, B. (Barbara), Koskeridis, F. (Fotios), Welsh, P. (Paul), Alizadeh, B. Z. (Behrooz Z.), Chasman, D. I. (Daniel I.), Sattar, N. (Naveed), Chadeau-Hyam, M. (Marc), Evangelou, E. (Evangelos), Järvelin, M.-R. (Marjo-Riitta), Elliott, P. (Paul), Tzoulaki, I. (Ioanna), Dehghan, A. (Abbas), Said, S. (Saredo), Pazoki, R. (Raha), Karhunen, V. (Ville), Võsa, U. (Urmo), Ligthart, S. (Symen), Bodinier, B. (Barbara), Koskeridis, F. (Fotios), Welsh, P. (Paul), Alizadeh, B. Z. (Behrooz Z.), Chasman, D. I. (Daniel I.), Sattar, N. (Naveed), Chadeau-Hyam, M. (Marc), Evangelou, E. (Evangelos), Järvelin, M.-R. (Marjo-Riitta), Elliott, P. (Paul), Tzoulaki, I. (Ioanna), and Dehghan, A. (Abbas)
Abstract: Chronic low-grade inflammation is linked to a multitude of chronic diseases. We report the largest genome-wide association study (GWAS) on C-reactive protein (CRP), a marker of systemic inflammation, in UK Biobank participants (N = 427,367, European descent) and the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium (total N = 575,531 European descent). We identify 266 independent loci, of which 211 are not previously reported. Gene-set analysis highlighted 42 gene sets associated with CRP levels (p ≤ 3.2 ×10−6) and tissue expression analysis indicated a strong association of CRP related genes with liver and whole blood gene expression. Phenome-wide association study identified 27 clinical outcomes associated with genetically determined CRP and subsequent Mendelian randomisation analyses supported a causal association with schizophrenia, chronic airway obstruction and prostate cancer. Our findings identified genetic loci and functional properties of chronic low-grade inflammation and provided evidence for causal associations with a range of diseases.
Published: 2022

2. The trans-ancestral genomic architecture of glycemic traits

Author: Chen, J. (Ji), Spracklen, C. N. (Cassandra N.), Marenne, G. (Gaelle), Varshney, A. (Arushi), Corbin, L. J. (Laura J.), Luan, J. (Jian'an), Willems, S. M. (Sara M.), Wu, Y. (Ying), Zhang, X. (Xiaoshuai), Horikoshi, M. (Momoko), Boutin, T. S. (Thibaud S.), Magi, R. (Reedik), Waage, J. (Johannes), Li-Gao, R. (Ruifang), Chan, K. H. (Kei Hang Katie), Yao, J. (Jie), Anasanti, M. D. (Mila D.), Chu, A. Y. (Audrey Y.), Claringbould, A. (Annique), Heikkinen, J. (Jani), Hong, J. (Jaeyoung), Hottenga, J.-J. (Jouke-Jan), Huo, S. (Shaofeng), Kaakinen, M. A. (Marika A.), Louie, T. (Tin), Maerz, W. (Winfried), Moreno-Macias, H. (Hortensia), Ndungu, A. (Anne), Nelson, S. C. (Sarah C.), Nolte, I. M. (Ilja M.), North, K. E. (Kari E.), Raulerson, C. K. (Chelsea K.), Ray, D. (Debashree), Rohde, R. (Rebecca), Rybin, D. (Denis), Schurmann, C. (Claudia), Sim, X. (Xueling), Southam, L. (Lorraine), Stewart, I. D. (Isobel D.), Wang, C. A. (Carol A.), Wang, Y. (Yujie), Wu, P. (Peitao), Zhang, W. (Weihua), Ahluwalia, T. S. (Tarunveer S.), Appel, E. V. (Emil V. R.), Bielak, L. F. (Lawrence F.), Brody, J. A. (Jennifer A.), Burtt, N. P. (Noel P.), Cabrera, C. P. (Claudia P.), Cade, B. E. (Brian E.), Chai, J. F. (Jin Fang), Chai, X. (Xiaoran), Chang, L.-C. (Li-Ching), Chen, C.-H. (Chien-Hsiun), Chen, B. H. (Brian H.), Chitrala, K. N. (Kumaraswamy Naidu), Chiu, Y.-F. (Yen-Feng), de Haan, H. G. (Hugoline G.), Delgado, G. E. (Graciela E.), Demirkan, A. (Ayse), Duan, Q. (Qing), Engmann, J. (Jorgen), Fatumo, S. A. (Segun A.), Gayan, J. (Javier), Giulianini, F. (Franco), Gong, J. H. (Jung Ho), Gustafsson, S. (Stefan), Hai, Y. (Yang), Hartwig, F. P. (Fernando P.), He, J. (Jing), Heianza, Y. (Yoriko), Huang, T. (Tao), Huerta-Chagoya, A. (Alicia), Hwang, M. Y. (Mi Yeong), Jensen, R. A. (Richard A.), Kawaguchi, T. (Takahisa), Kentistou, K. A. (Katherine A.), Kim, Y. J. (Young Jin), Kleber, M. E. (Marcus E.), Kooner, I. K. (Ishminder K.), Lai, S. (Shuiqing), Lange, L. A. (Leslie A.), Langefeld, C. D. (Carl D.), Lauzon, M. (Marie), Li, M. (Man), Ligthart, S. (Symen), Liu, J. (Jun), Loh, M. (Marie), Long, J. (Jirong), Lyssenko, V. (Valeriya), Mangino, M. (Massimo), Marzi, C. (Carola), Montasser, M. E. (May E.), Nag, A. (Abhishek), Nakatochi, M. (Masahiro), Noce, D. (Damia), Noordam, R. (Raymond), Pistis, G. (Giorgio), Preuss, M. (Michael), Raffield, L. (Laura), Rasmussen-Torvik, L. J. (Laura J.), Rich, S. S. (Stephen S.), Robertson, N. R. (Neil R.), Rueedi, R. (Rico), Ryan, K. (Kathleen), Sanna, S. (Serena), Saxena, R. (Richa), Schraut, K. E. (Katharina E.), Sennblad, B. (Bengt), Setoh, K. (Kazuya), Smith, A. V. (Albert V.), Sparso, T. (Thomas), Strawbridge, R. J. (Rona J.), Takeuchi, F. (Fumihiko), Tan, J. (Jingyi), Trompet, S. (Stella), van den Akker, E. (Erik), van der Most, P. J. (Peter J.), Verweij, N. (Niek), Vogel, M. (Mandy), Wang, H. (Heming), Wang, C. (Chaolong), Wang, N. (Nan), Warren, H. R. (Helen R.), Wen, W. (Wanqing), Wilsgaard, T. (Tom), Wong, A. (Andrew), Wood, A. R. (Andrew R.), Xie, T. (Tian), Zafarmand, M. H. (Mohammad Hadi), Zhao, J.-H. (Jing-Hua), Zhao, W. (Wei), Amin, N. (Najaf), Arzumanyan, Z. (Zorayr), Astrup, A. (Arne), Bakker, S. J. (Stephan J. L.), Baldassarre, D. (Damiano), Beekman, M. (Marian), Bergman, R. N. (Richard N.), Bertoni, A. (Alain), Blueher, M. (Matthias), Bonnycastle, L. L. (Lori L.), Bornstein, S. R. (Stefan R.), Bowden, D. W. (Donald W.), Cai, Q. (Qiuyin), Campbell, A. (Archie), Campbell, H. (Harry), Chang, Y. C. (Yi Cheng), de Geus, E. J. (Eco J. C.), Dehghan, A. (Abbas), Du, S. (Shufa), Eiriksdottir, G. (Gudny), Farmaki, A. E. (Aliki Eleni), Franberg, M. (Mattias), Fuchsberger, C. (Christian), Gao, Y. (Yutang), Gjesing, A. P. (Anette P.), Goel, A. (Anuj), Han, S. (Sohee), Hartman, C. A. (Catharina A.), Herder, C. (Christian), Hicks, A. A. (Andrew A.), Hsieh, C.-H. (Chang-Hsun), Hsueh, W. A. (Willa A.), Ichihara, S. (Sahoko), Igase, M. (Michiya), Ikram, M. A. (M. Arfan), Johnson, W. C. (W. Craig), Jorgensen, M. E. (Marit E.), Joshi, P. K. (Peter K.), Kalyani, R. R. (Rita R.), Kandeel, F. R. (Fouad R.), Katsuya, T. (Tomohiro), Khor, C. C. (Chiea Chuen), Kiess, W. (Wieland), Kolcic, I. (Ivana), Kuulasmaa, T. (Teemu), Kuusisto, J. (Johanna), Lall, K. (Kristi), Lam, K. (Kelvin), Lawlor, D. A. (Deborah A.), Lee, N. R. (Nanette R.), Lemaitre, R. N. (Rozenn N.), Li, H. (Honglan), Lin, S.-Y. (Shih-Yi), Lindstrom, J. (Jaana), Linneberg, A. (Allan), Liu, J. (Jianjun), Lorenzo, C. (Carlos), Matsubara, T. (Tatsuaki), Matsuda, F. (Fumihiko), Mingrone, G. (Geltrude), Mooijaart, S. (Simon), Moon, S. (Sanghoon), Nabika, T. (Toru), Nadkarni, G. N. (Girish N.), Nadler, J. L. (Jerry L.), Nelis, M. (Mari), Neville, M. J. (Matt J.), Norris, J. M. (Jill M.), Ohyagi, Y. (Yasumasa), Peters, A. (Annette), Peyser, P. A. (Patricia A.), Polasek, O. (Ozren), Qi, Q. (Qibin), Raven, D. (Dennis), Reilly, D. F. (Dermot F.), Reiner, A. (Alex), Rivideneira, F. (Fernando), Roll, K. (Kathryn), Rudan, I. (Igor), Sabanayagam, C. (Charumathi), Sandow, K. (Kevin), Sattar, N. (Naveed), Schuermann, A. (Annette), Shi, J. (Jinxiu), Stringham, H. M. (Heather M.), Taylor, K. D. (Kent D.), Teslovich, T. M. (Tanya M.), Thuesen, B. (Betina), Timmers, P. R. (Paul R. H. J.), Tremoli, E. (Elena), Tsai, M. Y. (Michael Y.), Uitterlinden, A. (Andre), van Dam, R. M. (Rob M.), van Heemst, D. (Diana), van Hylckama Vlieg, A. (Astrid), van Vliet-Ostaptchouk, J. V. (Jana V.), Vangipurapu, J. (Jagadish), Vestergaard, H. (Henrik), Wang, T. (Tao), Willems van Dijk, K. (Ko), Zemunik, T. (Tatijana), Abecasis, G. R. (Goncalo R.), Adair, L. S. (Linda S.), Aguilar-Salinas, C. A. (Carlos Alberto), Alarcon-Riquelme, M. E. (Marta E.), An, P. (Ping), Aviles-Santa, L. (Larissa), Becker, D. M. (Diane M.), Beilin, L. J. (Lawrence J.), Bergmann, S. (Sven), Bisgaard, H. (Hans), Black, C. (Corri), Boehnke, M. (Michael), Boerwinkle, E. (Eric), Boehm, B. O. (Bernhard O.), Bonnelykke, K. (Klaus), Boomsma, D. I. (D. I.), Bottinger, E. P. (Erwin P.), Buchanan, T. A. (Thomas A.), Canouil, M. (Mickael), Caulfield, M. J. (Mark J.), Chambers, J. C. (John C.), Chasman, D. I. (Daniel I.), Chen, Y. I. (Yii-Der Ida), Cheng, C.-Y. (Ching-Yu), Collins, F. S. (Francis S.), Correa, A. (Adolfo), Cucca, F. (Francesco), de Silva, H. J. (H. Janaka), Dedoussis, G. (George), Elmstahl, S. (Solve), Evans, M. K. (Michele K.), Ferrannini, E. (Ele), Ferrucci, L. (Luigi), Florez, J. C. (Jose C.), Franks, P. W. (Paul W.), Frayling, T. M. (Timothy M.), Froguel, P. (Philippe), Gigante, B. (Bruna), Goodarzi, M. O. (Mark O.), Gordon-Larsen, P. (Penny), Grallert, H. (Harald), Grarup, N. (Niels), Grimsgaard, S. (Sameline), Groop, L. (Leif), Gudnason, V. (Vilmundur), Guo, X. (Xiuqing), Hamsten, A. (Anders), Hansen, T. (Torben), Hayward, C. (Caroline), Heckbert, S. R. (Susan R.), Horta, B. L. (Bernardo L.), Huang, W. (Wei), Ingelsson, E. (Erik), James, P. S. (Pankow S.), Järvelin, M.-R. (Marjo-Ritta), Jonas, J. B. (Jost B.), Jukema, J. W. (J. Wouter), Kaleebu, P. (Pontiano), Kaplan, R. (Robert), Kardia, S. L. (Sharon L. R.), Kato, N. (Norihiro), Keinanen-Kiukaanniemi, S. M. (Sirkka M.), Kim, B.-J. (Bong-Jo), Kivimaki, M. (Mika), Koistinen, H. A. (Heikki A.), Kooner, J. S. (Jaspal S.), Koerner, A. (Antje), Kovacs, P. (Peter), Kuh, D. (Diana), Kumari, M. (Meena), Kutalik, Z. (Zoltan), Laakso, M. (Markku), Lakka, T. A. (Timo A.), Launer, L. J. (Lenore J.), Leander, K. (Karin), Li, H. (Huaixing), Lin, X. (Xu), Lind, L. (Lars), Lindgren, C. (Cecilia), Liu, S. (Simin), Loos, R. J. (Ruth J. F.), Magnusson, P. K. (Patrik K. E.), Mahajan, A. (Anubha), Metspalu, A. (Andres), Mook-Kanamori, D. O. (Dennis O.), Mori, T. A. (Trevor A.), Munroe, P. B. (Patricia B.), Njolstad, I. (Inger), O'Connell, J. R. (Jeffrey R.), Oldehinkel, A. J. (Albertine J.), Ong, K. K. (Ken K.), Padmanabhan, S. (Sandosh), Palmer, C. N. (Colin N. A.), Palmer, N. D. (Nicholette D.), Pedersen, O. (Oluf), Pennell, C. E. (Craig E.), Porteous, D. J. (David J.), Pramstaller, P. P. (Peter P.), Province, M. A. (Michael A.), Psaty, B. M. (Bruce M.), Qi, L. (Lu), Raffel, L. J. (Leslie J.), Rauramaa, R. (Rainer), Redline, S. (Susan), Ridker, P. M. (Paul M.), Rosendaal, F. R. (Frits R.), Saaristo, T. E. (Timo E.), Sandhu, M. (Manjinder), Saramies, J. (Jouko), Schneiderman, N. (Neil), Schwarz, P. (Peter), Scott, L. J. (Laura J.), Selvin, E. (Elizabeth), Sever, P. (Peter), Shu, X.-o. (Xiao-ou), Slagboom, P. E. (P. Eline), Small, K. S. (Kerrin S.), Smith, B. H. (Blair H.), Snieder, H. (Harold), Sofer, T. (Tamar), Sorensen, T. I. (Thorkild I. A.), Spector, T. D. (Tim D.), Stanton, A. (Alice), Steves, C. J. (Claire J.), Stumvoll, M. (Michael), Sun, L. (Liang), Tabara, Y. (Yasuharu), Tai, E. S. (E. Shyong), Timpson, N. J. (Nicholas J.), Tonjes, A. (Anke), Tuomilehto, J. (Jaakko), Tusie, T. (Teresa), Uusitupa, M. (Matti), van der Harst, P. (Pim), van Duijn, C. (Cornelia), Vitart, V. (Veronique), Vollenweider, P. (Peter), Vrijkotte, T. G. (Tanja G. M.), Wagenknecht, L. E. (Lynne E.), Walker, M. (Mark), Wang, Y. X. (Ya X.), Wareham, N. J. (Nick J.), Watanabe, R. M. (Richard M.), Watkins, H. (Hugh), Wei, W. B. (Wen B.), Wickremasinghe, A. R. (Ananda R.), Willemsen, G. (Gonneke), Wilson, J. F. (James F.), Wong, T.-Y. (Tien-Yin), Wu, J.-Y. (Jer-Yuarn), Xiang, A. H. (Anny H.), Yanek, L. R. (Lisa R.), Yengo, L. (Loic), Yokota, M. (Mitsuhiro), Zeggini, E. (Eleftheria), Zheng, W. (Wei), Zonderman, A. B. (Alan B.), Rotter, J. I. (Jerome I.), Gloyn, A. L. (Anna L.), McCarthy, M. I. (Mark I.), Dupuis, J. (Josee), Meigs, J. B. (James B.), Scott, R. A. (Robert A.), Prokopenko, I. (Inga), Leong, A. (Aaron), Liu, C.-T. (Ching-Ti), Parker, S. C. (Stephen C. J.), Mohlke, K. L. (Karen L.), Langenberg, C. (Claudia), Wheeler, E. (Eleanor), Morris, A. P. (Andrew P.), Barroso, I. (Ines), Chen, J. (Ji), Spracklen, C. N. (Cassandra N.), Marenne, G. (Gaelle), Varshney, A. (Arushi), Corbin, L. J. (Laura J.), Luan, J. (Jian'an), Willems, S. M. (Sara M.), Wu, Y. (Ying), Zhang, X. (Xiaoshuai), Horikoshi, M. (Momoko), Boutin, T. S. (Thibaud S.), Magi, R. (Reedik), Waage, J. (Johannes), Li-Gao, R. (Ruifang), Chan, K. H. (Kei Hang Katie), Yao, J. (Jie), Anasanti, M. D. (Mila D.), Chu, A. Y. (Audrey Y.), Claringbould, A. (Annique), Heikkinen, J. (Jani), Hong, J. (Jaeyoung), Hottenga, J.-J. (Jouke-Jan), Huo, S. (Shaofeng), Kaakinen, M. A. (Marika A.), Louie, T. (Tin), Maerz, W. (Winfried), Moreno-Macias, H. (Hortensia), Ndungu, A. (Anne), Nelson, S. C. (Sarah C.), Nolte, I. M. (Ilja M.), North, K. E. (Kari E.), Raulerson, C. K. (Chelsea K.), Ray, D. (Debashree), Rohde, R. (Rebecca), Rybin, D. (Denis), Schurmann, C. (Claudia), Sim, X. (Xueling), Southam, L. (Lorraine), Stewart, I. D. (Isobel D.), Wang, C. A. (Carol A.), Wang, Y. (Yujie), Wu, P. (Peitao), Zhang, W. (Weihua), Ahluwalia, T. S. (Tarunveer S.), Appel, E. V. (Emil V. R.), Bielak, L. F. (Lawrence F.), Brody, J. A. (Jennifer A.), Burtt, N. P. (Noel P.), Cabrera, C. P. (Claudia P.), Cade, B. E. (Brian E.), Chai, J. F. (Jin Fang), Chai, X. (Xiaoran), Chang, L.-C. (Li-Ching), Chen, C.-H. (Chien-Hsiun), Chen, B. H. (Brian H.), Chitrala, K. N. (Kumaraswamy Naidu), Chiu, Y.-F. (Yen-Feng), de Haan, H. G. (Hugoline G.), Delgado, G. E. (Graciela E.), Demirkan, A. (Ayse), Duan, Q. (Qing), Engmann, J. (Jorgen), Fatumo, S. A. (Segun A.), Gayan, J. (Javier), Giulianini, F. (Franco), Gong, J. H. (Jung Ho), Gustafsson, S. (Stefan), Hai, Y. (Yang), Hartwig, F. P. (Fernando P.), He, J. (Jing), Heianza, Y. (Yoriko), Huang, T. (Tao), Huerta-Chagoya, A. (Alicia), Hwang, M. Y. (Mi Yeong), Jensen, R. A. (Richard A.), Kawaguchi, T. (Takahisa), Kentistou, K. A. (Katherine A.), Kim, Y. J. (Young Jin), Kleber, M. E. (Marcus E.), Kooner, I. K. (Ishminder K.), Lai, S. (Shuiqing), Lange, L. A. (Leslie A.), Langefeld, C. D. (Carl D.), Lauzon, M. (Marie), Li, M. (Man), Ligthart, S. (Symen), Liu, J. (Jun), Loh, M. (Marie), Long, J. (Jirong), Lyssenko, V. (Valeriya), Mangino, M. (Massimo), Marzi, C. (Carola), Montasser, M. E. (May E.), Nag, A. (Abhishek), Nakatochi, M. (Masahiro), Noce, D. (Damia), Noordam, R. (Raymond), Pistis, G. (Giorgio), Preuss, M. (Michael), Raffield, L. (Laura), Rasmussen-Torvik, L. J. (Laura J.), Rich, S. S. (Stephen S.), Robertson, N. R. (Neil R.), Rueedi, R. (Rico), Ryan, K. (Kathleen), Sanna, S. (Serena), Saxena, R. (Richa), Schraut, K. E. (Katharina E.), Sennblad, B. (Bengt), Setoh, K. (Kazuya), Smith, A. V. (Albert V.), Sparso, T. (Thomas), Strawbridge, R. J. (Rona J.), Takeuchi, F. (Fumihiko), Tan, J. (Jingyi), Trompet, S. (Stella), van den Akker, E. (Erik), van der Most, P. J. (Peter J.), Verweij, N. (Niek), Vogel, M. (Mandy), Wang, H. (Heming), Wang, C. (Chaolong), Wang, N. (Nan), Warren, H. R. (Helen R.), Wen, W. (Wanqing), Wilsgaard, T. (Tom), Wong, A. (Andrew), Wood, A. R. (Andrew R.), Xie, T. (Tian), Zafarmand, M. H. (Mohammad Hadi), Zhao, J.-H. (Jing-Hua), Zhao, W. (Wei), Amin, N. (Najaf), Arzumanyan, Z. (Zorayr), Astrup, A. (Arne), Bakker, S. J. (Stephan J. L.), Baldassarre, D. (Damiano), Beekman, M. (Marian), Bergman, R. N. (Richard N.), Bertoni, A. (Alain), Blueher, M. (Matthias), Bonnycastle, L. L. (Lori L.), Bornstein, S. R. (Stefan R.), Bowden, D. W. (Donald W.), Cai, Q. (Qiuyin), Campbell, A. (Archie), Campbell, H. (Harry), Chang, Y. C. (Yi Cheng), de Geus, E. J. (Eco J. C.), Dehghan, A. (Abbas), Du, S. (Shufa), Eiriksdottir, G. (Gudny), Farmaki, A. E. (Aliki Eleni), Franberg, M. (Mattias), Fuchsberger, C. (Christian), Gao, Y. (Yutang), Gjesing, A. P. (Anette P.), Goel, A. (Anuj), Han, S. (Sohee), Hartman, C. A. (Catharina A.), Herder, C. (Christian), Hicks, A. A. (Andrew A.), Hsieh, C.-H. (Chang-Hsun), Hsueh, W. A. (Willa A.), Ichihara, S. (Sahoko), Igase, M. (Michiya), Ikram, M. A. (M. Arfan), Johnson, W. C. (W. Craig), Jorgensen, M. E. (Marit E.), Joshi, P. K. (Peter K.), Kalyani, R. R. (Rita R.), Kandeel, F. R. (Fouad R.), Katsuya, T. (Tomohiro), Khor, C. C. (Chiea Chuen), Kiess, W. (Wieland), Kolcic, I. (Ivana), Kuulasmaa, T. (Teemu), Kuusisto, J. (Johanna), Lall, K. (Kristi), Lam, K. (Kelvin), Lawlor, D. A. (Deborah A.), Lee, N. R. (Nanette R.), Lemaitre, R. N. (Rozenn N.), Li, H. (Honglan), Lin, S.-Y. (Shih-Yi), Lindstrom, J. (Jaana), Linneberg, A. (Allan), Liu, J. (Jianjun), Lorenzo, C. (Carlos), Matsubara, T. (Tatsuaki), Matsuda, F. (Fumihiko), Mingrone, G. (Geltrude), Mooijaart, S. (Simon), Moon, S. (Sanghoon), Nabika, T. (Toru), Nadkarni, G. N. (Girish N.), Nadler, J. L. (Jerry L.), Nelis, M. (Mari), Neville, M. J. (Matt J.), Norris, J. M. (Jill M.), Ohyagi, Y. (Yasumasa), Peters, A. (Annette), Peyser, P. A. (Patricia A.), Polasek, O. (Ozren), Qi, Q. (Qibin), Raven, D. (Dennis), Reilly, D. F. (Dermot F.), Reiner, A. (Alex), Rivideneira, F. (Fernando), Roll, K. (Kathryn), Rudan, I. (Igor), Sabanayagam, C. (Charumathi), Sandow, K. (Kevin), Sattar, N. (Naveed), Schuermann, A. (Annette), Shi, J. (Jinxiu), Stringham, H. M. (Heather M.), Taylor, K. D. (Kent D.), Teslovich, T. M. (Tanya M.), Thuesen, B. (Betina), Timmers, P. R. (Paul R. H. J.), Tremoli, E. (Elena), Tsai, M. Y. (Michael Y.), Uitterlinden, A. (Andre), van Dam, R. M. (Rob M.), van Heemst, D. (Diana), van Hylckama Vlieg, A. (Astrid), van Vliet-Ostaptchouk, J. V. (Jana V.), Vangipurapu, J. (Jagadish), Vestergaard, H. (Henrik), Wang, T. (Tao), Willems van Dijk, K. (Ko), Zemunik, T. (Tatijana), Abecasis, G. R. (Goncalo R.), Adair, L. S. (Linda S.), Aguilar-Salinas, C. A. (Carlos Alberto), Alarcon-Riquelme, M. E. (Marta E.), An, P. (Ping), Aviles-Santa, L. (Larissa), Becker, D. M. (Diane M.), Beilin, L. J. (Lawrence J.), Bergmann, S. (Sven), Bisgaard, H. (Hans), Black, C. (Corri), Boehnke, M. (Michael), Boerwinkle, E. (Eric), Boehm, B. O. (Bernhard O.), Bonnelykke, K. (Klaus), Boomsma, D. I. (D. I.), Bottinger, E. P. (Erwin P.), Buchanan, T. A. (Thomas A.), Canouil, M. (Mickael), Caulfield, M. J. (Mark J.), Chambers, J. C. (John C.), Chasman, D. I. (Daniel I.), Chen, Y. I. (Yii-Der Ida), Cheng, C.-Y. (Ching-Yu), Collins, F. S. (Francis S.), Correa, A. (Adolfo), Cucca, F. (Francesco), de Silva, H. J. (H. Janaka), Dedoussis, G. (George), Elmstahl, S. (Solve), Evans, M. K. (Michele K.), Ferrannini, E. (Ele), Ferrucci, L. (Luigi), Florez, J. C. (Jose C.), Franks, P. W. (Paul W.), Frayling, T. M. (Timothy M.), Froguel, P. (Philippe), Gigante, B. (Bruna), Goodarzi, M. O. (Mark O.), Gordon-Larsen, P. (Penny), Grallert, H. (Harald), Grarup, N. (Niels), Grimsgaard, S. (Sameline), Groop, L. (Leif), Gudnason, V. (Vilmundur), Guo, X. (Xiuqing), Hamsten, A. (Anders), Hansen, T. (Torben), Hayward, C. (Caroline), Heckbert, S. R. (Susan R.), Horta, B. L. (Bernardo L.), Huang, W. (Wei), Ingelsson, E. (Erik), James, P. S. (Pankow S.), Järvelin, M.-R. (Marjo-Ritta), Jonas, J. B. (Jost B.), Jukema, J. W. (J. Wouter), Kaleebu, P. (Pontiano), Kaplan, R. (Robert), Kardia, S. L. (Sharon L. R.), Kato, N. (Norihiro), Keinanen-Kiukaanniemi, S. M. (Sirkka M.), Kim, B.-J. (Bong-Jo), Kivimaki, M. (Mika), Koistinen, H. A. (Heikki A.), Kooner, J. S. (Jaspal S.), Koerner, A. (Antje), Kovacs, P. (Peter), Kuh, D. (Diana), Kumari, M. (Meena), Kutalik, Z. (Zoltan), Laakso, M. (Markku), Lakka, T. A. (Timo A.), Launer, L. J. (Lenore J.), Leander, K. (Karin), Li, H. (Huaixing), Lin, X. (Xu), Lind, L. (Lars), Lindgren, C. (Cecilia), Liu, S. (Simin), Loos, R. J. (Ruth J. F.), Magnusson, P. K. (Patrik K. E.), Mahajan, A. (Anubha), Metspalu, A. (Andres), Mook-Kanamori, D. O. (Dennis O.), Mori, T. A. (Trevor A.), Munroe, P. B. (Patricia B.), Njolstad, I. (Inger), O'Connell, J. R. (Jeffrey R.), Oldehinkel, A. J. (Albertine J.), Ong, K. K. (Ken K.), Padmanabhan, S. (Sandosh), Palmer, C. N. (Colin N. A.), Palmer, N. D. (Nicholette D.), Pedersen, O. (Oluf), Pennell, C. E. (Craig E.), Porteous, D. J. (David J.), Pramstaller, P. P. (Peter P.), Province, M. A. (Michael A.), Psaty, B. M. (Bruce M.), Qi, L. (Lu), Raffel, L. J. (Leslie J.), Rauramaa, R. (Rainer), Redline, S. (Susan), Ridker, P. M. (Paul M.), Rosendaal, F. R. (Frits R.), Saaristo, T. E. (Timo E.), Sandhu, M. (Manjinder), Saramies, J. (Jouko), Schneiderman, N. (Neil), Schwarz, P. (Peter), Scott, L. J. (Laura J.), Selvin, E. (Elizabeth), Sever, P. (Peter), Shu, X.-o. (Xiao-ou), Slagboom, P. E. (P. Eline), Small, K. S. (Kerrin S.), Smith, B. H. (Blair H.), Snieder, H. (Harold), Sofer, T. (Tamar), Sorensen, T. I. (Thorkild I. A.), Spector, T. D. (Tim D.), Stanton, A. (Alice), Steves, C. J. (Claire J.), Stumvoll, M. (Michael), Sun, L. (Liang), Tabara, Y. (Yasuharu), Tai, E. S. (E. Shyong), Timpson, N. J. (Nicholas J.), Tonjes, A. (Anke), Tuomilehto, J. (Jaakko), Tusie, T. (Teresa), Uusitupa, M. (Matti), van der Harst, P. (Pim), van Duijn, C. (Cornelia), Vitart, V. (Veronique), Vollenweider, P. (Peter), Vrijkotte, T. G. (Tanja G. M.), Wagenknecht, L. E. (Lynne E.), Walker, M. (Mark), Wang, Y. X. (Ya X.), Wareham, N. J. (Nick J.), Watanabe, R. M. (Richard M.), Watkins, H. (Hugh), Wei, W. B. (Wen B.), Wickremasinghe, A. R. (Ananda R.), Willemsen, G. (Gonneke), Wilson, J. F. (James F.), Wong, T.-Y. (Tien-Yin), Wu, J.-Y. (Jer-Yuarn), Xiang, A. H. (Anny H.), Yanek, L. R. (Lisa R.), Yengo, L. (Loic), Yokota, M. (Mitsuhiro), Zeggini, E. (Eleftheria), Zheng, W. (Wei), Zonderman, A. B. (Alan B.), Rotter, J. I. (Jerome I.), Gloyn, A. L. (Anna L.), McCarthy, M. I. (Mark I.), Dupuis, J. (Josee), Meigs, J. B. (James B.), Scott, R. A. (Robert A.), Prokopenko, I. (Inga), Leong, A. (Aaron), Liu, C.-T. (Ching-Ti), Parker, S. C. (Stephen C. J.), Mohlke, K. L. (Karen L.), Langenberg, C. (Claudia), Wheeler, E. (Eleanor), Morris, A. P. (Andrew P.), and Barroso, I. (Ines)
Abstract: Glycemic traits are used to diagnose and monitor type 2 diabetes and cardiometabolic health. To date, most genetic studies of glycemic traits have focused on individuals of European ancestry. Here we aggregated genome-wide association studies comprising up to 281,416 individuals without diabetes (30% non-European ancestry) for whom fasting glucose, 2-h glucose after an oral glucose challenge, glycated hemoglobin and fasting insulin data were available. Trans-ancestry and single-ancestry meta-analyses identified 242 loci (99 novel; P < 5 x 10-8), 80% of which had no significant evidence of between-ancestry heterogeneity. Analyses restricted to individuals of European ancestry with equivalent sample size would have led to 24 fewer new loci. Compared with single-ancestry analyses, equivalent-sized trans-ancestry fine-mapping reduced the number of estimated variants in 99% credible sets by a median of 37.5%. Genomic-feature, gene-expression and gene-set analyses revealed distinct biological signatures for each trait, highlighting different underlying biological pathways. Our results increase our understanding of diabetes pathophysiology by using trans-ancestry studies for improved power and resolution.
Published: 2021

3. Lifetime risk to progress from pre-diabetes to type 2 diabetes among women and men: comparison between American

Author: Herpt, T.W. (Thijs) van, Ligthart, S. (Symen), Leening, M.J.G. (Maarten J G), Hoek, M. (Mandy) van, Lieverse, A.G. (Aloysius), Ikram, M.A. (Arfan), Sijbrands, E.J.G. (Eric J G), Dehghan, A. (Abbas), Kavousi, M. (Maryam), Herpt, T.W. (Thijs) van, Ligthart, S. (Symen), Leening, M.J.G. (Maarten J G), Hoek, M. (Mandy) van, Lieverse, A.G. (Aloysius), Ikram, M.A. (Arfan), Sijbrands, E.J.G. (Eric J G), Dehghan, A. (Abbas), and Kavousi, M. (Maryam)
Abstract: INTRODUCTION: Pre-diabetes, a status conferring high risk of overt diabetes, is defined differently by the American Diabetes Association (ADA) and the WHO. We investigated the impact of applying definitions of pre-diabetes on lifetime risk of diabetes in women and men from the general population. RESEARCH DESIGN AND METHODS: We used data from 8844 women without diabetes and men aged ≥45 years from the prospective population-based Rotterdam Study in the Netherlands. In both gender groups, we calculated pre-diabetes prevalence according to ADA and WHO criteria and estimated the 10-year and lifetime risk to progress to overt diabetes with adjustment for competing risk of death. RESULTS: Out of 8844 individuals, pre-diabetes was identified in 3492 individuals (prevalence 40%, 95% CI 38% to 41%) according to ADA and 1382 individuals (prevalence 16%, 95% CI 15% to 16%) according to WHO criteria. In both women and men and each age category, ADA prevalence estimates doubled WHO-defined pre-diabetes. For women and men aged 45 years having ADA-defined pre-diabetes, the 10-year risk of diabetes was 14.2% (95% CI 6.0% to 22.5%) and 9.2% (95% CI 3.4% to 15.0%) compared with 23.2% (95% CI 6.8% to 39.6%) and 24.6% (95% CI 8.4% to 40.8%) in women and men with WHO-defined pre-diabetes. At age 45 years, the remaining lifetime risk to progress to overt diabetes was 57.5% (95% CI 51.8% to 63.2%) vs 80.2% (95% CI 74.1% to 86.3%) in women and 46.1% (95% CI 40.8% to 51.4%) vs 68.4% (95% CI 58.3% to 78.5%) in men with pre-diabetes according to ADA and WHO definitions, respectively. CONCLUSION: Prevalence of pre-diabetes differed considerably in both women and men when applying ADA and WHO pre-diabetes definitions. Women with pre-diabetes had higher lifetime risk to progress to diabetes. The lifetime risk of diabetes was lower in women and men with ADA-defined pre-diabetes as compared with WHO. Improvement of pre-diabetes definition considering appropriate sex-specific and age-specific glyc
Published: 2020
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4. Molecular Epidemiology of Inflammation: Link with Type 2 Diabetes and Coronary Heart Disease

Author: Ligthart, S. (Symen) and Ligthart, S. (Symen)
Abstract: This thesis presents the genetics and epigenetics of inflammation, and the link with type 2 diabetes and cardiovascular disease is investigated.
Published: 2020

5. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

Author: Liu, J. (Jun), Carnero-Montoro, E. (Elena), Dongen, J. (Jenny) van, Lent, S. (Samantha), Prokić, I. (Ivana), Ligthart, S. (Symen), Tsai, P.-C. (Pei-Chien), Martin, T.C. (Tiphaine C.), Mandaviya, P.R. (Pooja), Jansen, R. (Rick), Peters, M.A.D. (Marjolein), Duijts, L. (Liesbeth), Jaddoe, V.W.V. (Vincent), Tiemeier, H.W. (Henning), Felix, J.F. (Janine), Willemsen, G.A.H.M. (Gonneke), Geus, E.J.C. (Eco) de, Chu, A.Y. (Audrey), Levy, D. (Daniel), Hwang, S.-J. (Shih-Jen), Bressler, J. (Jan), Gondalia, R. (Rahul), Salfati, E. (Elias), Herder, C. (Christian), Hidalgo, B. (Bertha), Tanaka, T. (Toshiko), Moore, A.Z. (Ann Zenobia), Lemaitre, R.N. (Rozenn N.), Jhun, M.A. (Min A.), Smith, J.A. (Jennifer A), Sotoodehnia, N. (Nona), Bandinelli, S. (Stefania), Ferrucci, L. (Luigi), Arnett, D.K. (Donna), Grallert, H. (Harald), Assimes, T.L. (Themistocles L.), Hou, L. (Lifang), Baccarelli, A.A. (Andrea), Whitsel, E.A. (Eric), van Dijk, K.W. (Ko Willems), Amin, N. (Najaf), Uitterlinden, A.G. (André), Sijbrands, E.J.G. (Eric), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Spector, T.D. (Timothy), Hivert, M.-F. (Marie-France), Rotter, J.I. (Jerome I.), Meigs, J.B. (James), Palmer, C.N.A. (Colin), Meurs, J.B.J. (Joyce) van, Isaacs, A.J. (Aaron), Boomsma, D.I. (Dorret I.), Bell, J.T. (Jordana T.), Demirkan, A. (Ayşe), Duijn, C.M. (Cornelia) van, Liu, J. (Jun), Carnero-Montoro, E. (Elena), Dongen, J. (Jenny) van, Lent, S. (Samantha), Prokić, I. (Ivana), Ligthart, S. (Symen), Tsai, P.-C. (Pei-Chien), Martin, T.C. (Tiphaine C.), Mandaviya, P.R. (Pooja), Jansen, R. (Rick), Peters, M.A.D. (Marjolein), Duijts, L. (Liesbeth), Jaddoe, V.W.V. (Vincent), Tiemeier, H.W. (Henning), Felix, J.F. (Janine), Willemsen, G.A.H.M. (Gonneke), Geus, E.J.C. (Eco) de, Chu, A.Y. (Audrey), Levy, D. (Daniel), Hwang, S.-J. (Shih-Jen), Bressler, J. (Jan), Gondalia, R. (Rahul), Salfati, E. (Elias), Herder, C. (Christian), Hidalgo, B. (Bertha), Tanaka, T. (Toshiko), Moore, A.Z. (Ann Zenobia), Lemaitre, R.N. (Rozenn N.), Jhun, M.A. (Min A.), Smith, J.A. (Jennifer A), Sotoodehnia, N. (Nona), Bandinelli, S. (Stefania), Ferrucci, L. (Luigi), Arnett, D.K. (Donna), Grallert, H. (Harald), Assimes, T.L. (Themistocles L.), Hou, L. (Lifang), Baccarelli, A.A. (Andrea), Whitsel, E.A. (Eric), van Dijk, K.W. (Ko Willems), Amin, N. (Najaf), Uitterlinden, A.G. (André), Sijbrands, E.J.G. (Eric), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Spector, T.D. (Timothy), Hivert, M.-F. (Marie-France), Rotter, J.I. (Jerome I.), Meigs, J.B. (James), Palmer, C.N.A. (Colin), Meurs, J.B.J. (Joyce) van, Isaacs, A.J. (Aaron), Boomsma, D.I. (Dorret I.), Bell, J.T. (Jordana T.), Demirkan, A. (Ayşe), and Duijn, C.M. (Cornelia) van
Abstract: Despite existing reports on differential DNA methylation in type 2 diabetes (T2D) and obesity, our understanding of its functional relevance remains limited. Here we show the effect of differential methylation in the early phases of T2D pathology by a blood-based epigenome-wide association study of 4808 non-diabetic Europeans in the discovery phase and 11,750 individuals in the replication. We identify CpGs in LETM1, RBM20, IRS2, MAN2A2 and the 1q25.3 region associated with fasting insulin, and in FCRL6, SLAMF1, APOBEC3H and the 15q26.1 region with fasting glucose. In silico cross-omics analyses highlight the role of differential methylation in the crosstalk between the adaptive immune system and glucose homeostasis. The differential methylation explains at least 16.9% of the association between obesity and insulin. Our study sheds light on the biological interactions between genetic variants driving differential methylation and gene expression in the early pathogenesis of T2D.
Published: 2019
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6. Association of methylation signals with incident coronary heart disease in an epigenome-wide assessment of circulating tumor necrosis factor α

Author: Aslibekyan, S. (Stella), Agha, G. (Golareh), Colicino, E. (Elena), Do, A. N. (Anh N.), Lahti, J. (Jari), Ligthart, S. (Symen), Marioni, R. E. (Riccardo E.), Marzi, C. (Carola), Mendelson, M. M. (Michael M.), Tanaka, T. (Toshiko), Wielscher, M. (Matthias), Absher, D. M. (Devin M.), Ferrucci, L. (Luigi), Franco, O. H. (Oscar H.), Gieger, C. (Christian), Grallert, H. (Harald), Hernandez, D. (Dena), Huan, T. (Tianxiao), Iurato, S. (Stella), Joehanes, R. (Roby), Just, A. C. (Allan C.), Kunze, S. (Sonja), Lin, H. (Honghuang), Liu, C. (Chunyu), Meigs, J. B. (James B.), van Meurs, J. B. (Joyce B.J.), Moore, A. Z. (Ann Zenobia), Peters, A. (Annette), Prokisch, H. (Holger), Räikkönen, K. (Katri), Rathmann, W. (Wolfgang), Roden, M. (Michael), Schramm, K. (Katharina), Schwartz, J. D. (Joel D.), Starr, J. M. (John M.), Uitterlinden, A. G. (André G.), Vokonas, P. (Pantel), Waldenberger, M. (Melanie), Yao, C. (Chen), Zhi, D. (Degui), Baccarelli, A. A. (Andrea A.), Bandinelli, S. (Stefania), Deary, I. J. (Ian J.), Dehghan, A. (Abbas), Eriksson, J. (Johan), Herder, C. (Christian), Järvelin, M.-R. (Marjo-Riitta), Levy, D. (Daniel), Arnett, D. K. (Donna K.), Aslibekyan, S. (Stella), Agha, G. (Golareh), Colicino, E. (Elena), Do, A. N. (Anh N.), Lahti, J. (Jari), Ligthart, S. (Symen), Marioni, R. E. (Riccardo E.), Marzi, C. (Carola), Mendelson, M. M. (Michael M.), Tanaka, T. (Toshiko), Wielscher, M. (Matthias), Absher, D. M. (Devin M.), Ferrucci, L. (Luigi), Franco, O. H. (Oscar H.), Gieger, C. (Christian), Grallert, H. (Harald), Hernandez, D. (Dena), Huan, T. (Tianxiao), Iurato, S. (Stella), Joehanes, R. (Roby), Just, A. C. (Allan C.), Kunze, S. (Sonja), Lin, H. (Honghuang), Liu, C. (Chunyu), Meigs, J. B. (James B.), van Meurs, J. B. (Joyce B.J.), Moore, A. Z. (Ann Zenobia), Peters, A. (Annette), Prokisch, H. (Holger), Räikkönen, K. (Katri), Rathmann, W. (Wolfgang), Roden, M. (Michael), Schramm, K. (Katharina), Schwartz, J. D. (Joel D.), Starr, J. M. (John M.), Uitterlinden, A. G. (André G.), Vokonas, P. (Pantel), Waldenberger, M. (Melanie), Yao, C. (Chen), Zhi, D. (Degui), Baccarelli, A. A. (Andrea A.), Bandinelli, S. (Stefania), Deary, I. J. (Ian J.), Dehghan, A. (Abbas), Eriksson, J. (Johan), Herder, C. (Christian), Järvelin, M.-R. (Marjo-Riitta), Levy, D. (Daniel), and Arnett, D. K. (Donna K.)
Abstract: Importance: Tumor necrosis factor α (TNF-α) is a proinflammatory cytokine with manifold consequences for mammalian pathophysiology, including cardiovascular disease. A deeper understanding of TNF-α biology may enhance treatment precision. Objective: To conduct an epigenome-wide analysis of blood-derived DNA methylation and TNF-α levels and to assess the clinical relevance of findings. Design, Setting, and Participants: This meta-analysis assessed epigenome-wide associations in circulating TNF-α concentrations from 5 cohort studies and 1 interventional trial, with replication in 3 additional cohort studies. Follow-up analyses investigated associations of identified methylation loci with gene expression and incident coronary heart disease; this meta-analysis included 11 461 participants who experienced 1895 coronary events. Exposures: Circulating TNF-α concentration. Main Outcomes and Measures: DNA methylation at approximately 450 000 loci, neighboring DNA sequence variation, gene expression, and incident coronary heart disease. Results: The discovery cohort included 4794 participants, and the replication study included 816 participants (overall mean [SD] age, 60.7 [8.5] years). In the discovery stage, circulating TNF-α levels were associated with methylation of 7 cytosine-phosphate-guanine (CpG) sites, 3 of which were located in or near DTX3L-PARP9 at cg00959259 (β [SE] = −0.01 [0.003]; P = 7.36×10⁻⁸), cg08122652 (β [SE] = −0.008 [0.002]; P = 2.24×10⁻⁷), and cg22930808(β [SE] = −0.01 [0.002]; P = 6.92×10⁻⁸); NLRC5 at cg16411857 (β [SE] = −0.01 [0.002]; P = 2.14×10⁻¹³) and cg07839457 (β [SE] = −0.02 [0.003]; P = 6.31×10⁻¹⁰); or ABO, at cg13683939 (β [SE] = 0.04 [0.008]; P = 1.42×10⁻⁷) and cg24267699 (β [SE] = −0.009 [0.002]; P = 1.67 × 10⁻⁷), after accounting for multiple testing. Of these, negative associations between TNF-α concentration and methylation of 2 loci in NLRC5 and 1 in DTX3L-14 PARP9 were replicated. Replicated TNF-α–linked CpG sites were associ
Published: 2018

7. Novel inflammatory markers for incident pre-diabetes and type 2 diabetes: the Rotterdam Study

Author: Brahimaj, A. (Adela), Ligthart, S. (Symen), Ghanbari, M. (Mohsen), Ikram, M.K. (Kamran), Hofman, A. (Albert), Franco, O.H. (Oscar), Kavousi, M. (Maryam), Dehghan, A. (Abbas), Brahimaj, A. (Adela), Ligthart, S. (Symen), Ghanbari, M. (Mohsen), Ikram, M.K. (Kamran), Hofman, A. (Albert), Franco, O.H. (Oscar), Kavousi, M. (Maryam), and Dehghan, A. (Abbas)
Abstract: The immune response involved in each phase of type 2 diabetes (T2D) development might be different. We aimed to identify novel inflammatory markers that predict progression from normoglycemia to pre-diabetes, incident T2D and insulin therapy. We used plasma levels of 26 inflammatory markers in 971 subjects from the Rotterdam Study. Among them 17 are novel and 9 previously studied. Cox regression models were built to perform survival analysis. Main Outcome Measures: During a follow-up of up to 14.7 years (between April 1, 1997, and Jan 1, 2012) 139 cases of pre-diabetes, 110 cases of T2D and 26 cases of insulin initiation were identified. In age and sex adjusted Cox models, IL13 (HR = 0.78), EN-RAGE (1.30), CFH (1.24), IL18 (1.22) and CRP (1.32) were associated with incident pre-diabetes. IL13 (0.62), IL17 (0.75), EN-RAGE (1.25), complement 3 (1.44), IL18 (1.35), TNFRII (1.27), IL1ra (1.24) and CRP (1.64) were associated with incident T2D. In multivariate models, IL13 (0.77), EN-RAGE (1.23) and CRP (1.26) remained associated with pre-diabetes. IL13 (0.67), IL17 (0.76) and CRP (1.32) remained associated with T2D. IL13 (0.55) was the only marker associated with initiation of insulin therapy in diabetics. Various inflammatory markers are associated with progression from normoglycemia to pre-diabetes (IL13, EN-RAGE, CRP), T2D (IL13, IL17, CRP) or insulin therapy start (IL13). Among them, EN-RAGE is a novel inflammatory marker for pre-diabetes, IL17 for incident T2D and IL13 for pre-diabetes, incident T2D and insulin therapy start.
Published: 2017
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8. Age at natural menopause and risk of type 2 diabetes

Author: Muka, T. (Taulant), Asllanaj, E. (Eralda), Avazverdi, N. (Naim), Jaspers, L. (Loes), Stringa, N. (Najada), Milic, J. (Jelena), Ligthart, S. (Symen), Ikram, M.K. (Kamran), Laven, J.S.E. (Joop), Kavousi, M. (Maryam), Dehghan, A. (Abbas), Franco, O.H. (Oscar), Muka, T. (Taulant), Asllanaj, E. (Eralda), Avazverdi, N. (Naim), Jaspers, L. (Loes), Stringa, N. (Najada), Milic, J. (Jelena), Ligthart, S. (Symen), Ikram, M.K. (Kamran), Laven, J.S.E. (Joop), Kavousi, M. (Maryam), Dehghan, A. (Abbas), and Franco, O.H. (Oscar)
Abstract: __Aims/hypothesis__ In this study, we aimed to examine the association between age at natural menopause and risk of type 2 diabetes, and to assess whether this association is independent of potential mediators. __Methods__ We included 3639 postmenopausal women from the prospective, population-based Rotterdam Study. Age at natural menopause was self-reported retrospectively and was treated as a continuous variable and in categories (premature, <40 years; early, 40–44 years; normal, 45–55 years; and late menopause, >55 years [reference]). Type 2 diabetes events were diagnosed on the basis of medical records and glucose measurements from RotterdamStudy visits. HRs and 95%CIs were calculated using Cox proportional hazards models, adjusted for confounding factors; in another model, they were additionally adjusted for potential mediators, including obesity, C-reactive protein, glucose and insulin, as well as for levels of total oestradiol and androgens. __Results__ During a median follow-up of 9.2 years, we identified 348 individuals with incident type 2 diabetes. After adjustment for confounders, HRs for type 2 diabetes were 3.7 (95% CI 1.8, 7.5), 2.4 (95% CI 1.3, 4.3) and 1.60 (95% CI 1.0, 2.8) for women with premature, early and normal menopause, respectively, relative to those with late menopause (ptrend <0.001). The HR for type 2 diabetes per 1 year older at menopause was 0.96 (95% CI 0.94, 0.98). Further adjustment for BMI, glycaemic traits, metabolic risk factors, C-reactive protein, endogenous sex hormone levels or shared genetic factors did not affect this association. __Conclusions/interpretation__ Early onset of natural menopause is an independent marker for type 2 diabetes in postmenopausal women.
Published: 2017
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9. Serum magnesium and the risk of prediabetes: a population-based cohort study

Author: Kieboom, B.C.T. (Brenda), Ligthart, S. (Symen), Dehghan, A. (Abbas), Kurstjens, S. (Steef), Baaij, J.H.F. (Jeroen) de, Franco, O.H. (Oscar), Hofman, A. (Albert), Zietse, R. (Bob), Stricker, B.H.Ch. (Bruno), Hoorn, E.J. (Ewout), Kieboom, B.C.T. (Brenda), Ligthart, S. (Symen), Dehghan, A. (Abbas), Kurstjens, S. (Steef), Baaij, J.H.F. (Jeroen) de, Franco, O.H. (Oscar), Hofman, A. (Albert), Zietse, R. (Bob), Stricker, B.H.Ch. (Bruno), and Hoorn, E.J. (Ewout)
Abstract: _Aims/hypothesis:_ Previous studies have found an association between serum magnesium and incident diabetes; however, this association may be due to reverse causation, whereby diabetes may induce urinary magnesium loss. In contrast, in prediabetes (defined as impaired fasting glucose), serum glucose levels are below the threshold for urinary magnesium wasting and, hence, unlikely to influence serum magnesium levels. Thus, to study the directionality of the association between serum magnesium levels and diabetes, we investigated its association with prediabetes. We also investigated whether magnesium-regulating genes influence diabetes risk through serum magnesium levels. Additionally, we quantified the effect of insulin resistance in the association between serum magnesium levels and diabetes risk. _Methods:_ Within the population-based Rotterdam Study, we used Cox models, adjusted for age, sex, lifestyle factors, comorbidities, kidney function, serum levels of electrolytes and diuretic use, to study the association between serum magnesium and prediabetes/diabetes. In addition, we performed two mediation analyses
Published: 2017
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10. Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study

Author: Vries, P.S. (Paul) de, Sabater-Lleal, M. (Maria), Chasman, D.I. (Daniel), Trompet, S. (Stella), Ahluwalia, T.S. (Tarunveer Singh), Teumer, A. (Alexander), Kleber, M.E. (Marcus), Chen, M.-H. (Ming-Huei), Wang, J.J. (Jie Jin), Attia, J. (John), Marioni, R.E. (Riccardo), Steri, M. (Maristella), Weng, L.-C. (Lu-Chen), Pool, R. (Reńe), Grossmann, V. (Vera), Brody, J.A. (Jennifer A.), Venturini, C. (Cristina), Tanaka, T. (Toshiko), Rose, L.M. (Lynda), Oldmeadow, C. (Christopher), Mazur, J. (Johanna), Basu, S. (Saonli), Frånberg, M. (Mattias), Yang, Q. (Qiong), Ligthart, S. (Symen), Hottenga, J.J. (Jouke Jan), Rumley, A. (Ann), Mulas, A. (Antonella), Craen, A.J. (Anton) de, Grotevendt, A. (Anne), Taylor, K.D. (Kent D.), Delgado, G., Kifley, A. (Annette), Lopez, L.M. (Lorna), Berentzen, T.L. (Tina L.), Mangino, M. (Massimo), Bandinelli, S. (Stefania), Morrison, A.C. (Alanna C.), Hamsten, A. (Anders), Tofler, G.H. (Geoffrey), Maat, M.P.M. (Moniek) de, Draisma, G. (Gerrit), Lowe, G.D. (Gordon D.), Zoledziewska, M. (Magdalena), Sattar, N. (Naveed), Lackner, K.J. (Karl J.), Völker, U. (Uwe), McKnight, B. (Barbara), Huang, J. (Jian), Holliday, E.G. (Elizabeth), McEvoy, M.A. (Mark A.), Starr, J.M. (John), Hysi, P.G. (Pirro), Hernandez, D.G. (Dena), Guan, W. (Weihua), Rivadeneira Ramirez, F. (Fernando), McArdle, W.L. (Wendy), Slagboom, P.E. (Eline), Zeller, T. (Tanja), Psaty, B.M. (Bruce), Uitterlinden, A.G. (André), Geus, E.J.C. (Eco) de, Stott, D.J. (David J.), Binder, H. (Harald), Hofman, A. (Albert), Franco, O.H. (Oscar), Rotter, J.I. (Jerome I.), Ferrucci, L. (Luigi), Spector, T.D. (Tim D.), Deary, I.J. (Ian), März, W. (Winfried), Greinacher, A. (Andreas), Wild, P.S. (Philipp S.), Cucca, F. (Francesco), Boomsma, D.I. (Dorret), Watkins, H. (Hugh), Tang, W. (Weihong), Ridker, P.M. (Paul), Jukema, J.W., Scott, R.J. (Rodney J.), Mitchell, P. (Paul), Hansen, T. (T.), O'Donnell, C.J. (Christopher J.), Smith, N.L. (Nicholas L.), Strachan, D.P. (David P.), Dehghan, A. (Abbas), Vries, P.S. (Paul) de, Sabater-Lleal, M. (Maria), Chasman, D.I. (Daniel), Trompet, S. (Stella), Ahluwalia, T.S. (Tarunveer Singh), Teumer, A. (Alexander), Kleber, M.E. (Marcus), Chen, M.-H. (Ming-Huei), Wang, J.J. (Jie Jin), Attia, J. (John), Marioni, R.E. (Riccardo), Steri, M. (Maristella), Weng, L.-C. (Lu-Chen), Pool, R. (Reńe), Grossmann, V. (Vera), Brody, J.A. (Jennifer A.), Venturini, C. (Cristina), Tanaka, T. (Toshiko), Rose, L.M. (Lynda), Oldmeadow, C. (Christopher), Mazur, J. (Johanna), Basu, S. (Saonli), Frånberg, M. (Mattias), Yang, Q. (Qiong), Ligthart, S. (Symen), Hottenga, J.J. (Jouke Jan), Rumley, A. (Ann), Mulas, A. (Antonella), Craen, A.J. (Anton) de, Grotevendt, A. (Anne), Taylor, K.D. (Kent D.), Delgado, G., Kifley, A. (Annette), Lopez, L.M. (Lorna), Berentzen, T.L. (Tina L.), Mangino, M. (Massimo), Bandinelli, S. (Stefania), Morrison, A.C. (Alanna C.), Hamsten, A. (Anders), Tofler, G.H. (Geoffrey), Maat, M.P.M. (Moniek) de, Draisma, G. (Gerrit), Lowe, G.D. (Gordon D.), Zoledziewska, M. (Magdalena), Sattar, N. (Naveed), Lackner, K.J. (Karl J.), Völker, U. (Uwe), McKnight, B. (Barbara), Huang, J. (Jian), Holliday, E.G. (Elizabeth), McEvoy, M.A. (Mark A.), Starr, J.M. (John), Hysi, P.G. (Pirro), Hernandez, D.G. (Dena), Guan, W. (Weihua), Rivadeneira Ramirez, F. (Fernando), McArdle, W.L. (Wendy), Slagboom, P.E. (Eline), Zeller, T. (Tanja), Psaty, B.M. (Bruce), Uitterlinden, A.G. (André), Geus, E.J.C. (Eco) de, Stott, D.J. (David J.), Binder, H. (Harald), Hofman, A. (Albert), Franco, O.H. (Oscar), Rotter, J.I. (Jerome I.), Ferrucci, L. (Luigi), Spector, T.D. (Tim D.), Deary, I.J. (Ian), März, W. (Winfried), Greinacher, A. (Andreas), Wild, P.S. (Philipp S.), Cucca, F. (Francesco), Boomsma, D.I. (Dorret), Watkins, H. (Hugh), Tang, W. (Weihong), Ridker, P.M. (Paul), Jukema, J.W., Scott, R.J. (Rodney J.), Mitchell, P. (Paul), Hansen, T. (T.), O'Donnell, C.J. (Christopher J.), Smith, N.L. (Nicholas L.), Strachan, D.P. (David P.), and Dehghan, A. (Abbas)
Abstract: An increasing number of genome-wide association (GWA) studies are now using the higher resolution 1000 Genomes Project reference panel (1000G) for imputation, with the expectation that 1000G imputation will lead to the discovery of additional associated loci when compared to HapMap imputation. In order to assess the improvement of 1000G over HapMap imputation in identifying associated loci, we compared the results of GWA studies of circulating fibrinogen based on the two reference panels. Using both HapMap and 1000G imputation we performed a meta-analysis of 22 studies comprising the same 91,953 individuals. We identified six additional signals using 1000G imputation, while 29 loci were associated using both HapMap and 1000G imputation. One locus identified using HapMap imputation was not significant using 1000G imputation. The genome-wide significance threshold of 5×10-8 is based on the number of independent statistical tests using HapMap imputation, and 1000G imputation may lead to further independent tests that should be corrected for. When using a stricter Bonferroni correction for the 1000G GWA study (P-value < 2.5×10-8), the number of loci significant only using HapMap imputation increased to 4 while the number of loci significant only using 1000G decreased to 5. In conclusion, 1000G imputation enabled the identification of 20% more loci than HapMap imputation, although the advantage of 1000G imputation became less clear when a stricter Bonferroni correction was used. More generally, our results provide insights that are applicable to the implementation of other dense reference panels that are under development.
Published: 2017
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11. ADAMTS13 activity as a novel risk factor for incident type 2 diabetes mellitus: a population-based cohort study

Author: Vries, P.S. (Paul) de, Herpt, T.W. (Thijs) van, Ligthart, S. (Symen), Hofman, A. (Albert), Ikram, M.A. (Arfan), Hoek, M. (Mandy) van, Sijbrands, E.J.G. (Eric), Franco, O.H. (Oscar), Maat, M.P.M. (Moniek) de, Leebeek, F.W.G. (Frank), Dehghan, A. (Abbas), Vries, P.S. (Paul) de, Herpt, T.W. (Thijs) van, Ligthart, S. (Symen), Hofman, A. (Albert), Ikram, M.A. (Arfan), Hoek, M. (Mandy) van, Sijbrands, E.J.G. (Eric), Franco, O.H. (Oscar), Maat, M.P.M. (Moniek) de, Leebeek, F.W.G. (Frank), and Dehghan, A. (Abbas)
Abstract: Aims/hypothesis: ADAMTS13 is a protease that breaks down von Willebrand factor (VWF) multimers into smaller, less active particles. VWF has been associated with an increased risk of incident type 2 diabetes mellitus. Here, we determine whether ADAMTS13 activity and VWF antigen are associated with incident diabetes. Methods: This study included 5176 participants from the Rotterdam Study, a prospective population-based cohort study. Participants were free of diabetes at baseline and followed up for more than 20 years. Cox proportional hazards models were used to examine the association of ADAMTS13 activity and VWF antigen with incident diabetes. Results: ADAMTS13 activity was associated with an increased risk of incident diabetes (HR 1.17 [95% CI 1.08, 1.27]) after adjust
Published: 2017
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12. Obesity and Life Expectancy with and without Diabetes in Adults Aged 55 Years and Older in the Netherlands: A Prospective Cohort Study

Author: Dhana, K. (Klodian), Nano, J. (Jana), Ligthart, S. (Symen), Peeters, A. (Anna), Hofman, A. (Albert), Nusselder, W.J. (Wilma), Dehghan, A. (Abbas), Franco, O.H. (Oscar), Dhana, K. (Klodian), Nano, J. (Jana), Ligthart, S. (Symen), Peeters, A. (Anna), Hofman, A. (Albert), Nusselder, W.J. (Wilma), Dehghan, A. (Abbas), and Franco, O.H. (Oscar)
Abstract: Background: Overweight and obesity are associated with increased risk of type 2 diabetes. Limited evidence exists regarding the effect of excess weight on years lived with and without diabetes. We aimed to determine the association of overweight and obesity with the number of years lived with and without diabetes in a middle-aged and elderly population. Methods and Findings: The study included 6,499 individuals (3,656 women) aged 55 y and older from the population-based Rotterdam Study. We developed a multistate life table to calculate life expectancy for individuals who were normal weight, overweight, and obese and the difference in years lived with and without diabetes. For life table calculations, we used prevalence, incidence rate, and hazard ratios (HRs) for three transitions (healthy to diabetes, healthy to death, and diabetes to death), stratifying by body mass index (BMI) at baseline and adjusting for confounders. During a median follow-up of 11.1 y, we observed 697 incident diabetes events and 2,192 overall deaths. Obesity was associated with an increased risk of developing diabetes (HR: 2.13 [p < 0.001] for men and 3.54 [p < 0.001] for women). Overweight and obesity were not associated with mortality in men and women with or without diabetes. Total life expectancy remained unaffected by overweight and obesity. Nevertheless, men with obesity aged 55 y and older lived 2.8 (95% CI −6.1 to −0.1) fewer y without diabetes than normal weight individuals, whereas, for women, the difference between obese and normal weight counterparts was 4.7 (95% CI −9.0 to −0.6) y. Men and women with obesity lived 2.8 (95% CI 0.6 to 6.2) and 5.3
Published: 2016
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13. Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation

Author: Ligthart, S. (Symen), Vaez, A. (Ahmad), Hsu, Y.-H. (Yi-Hsiang), Stolk, R.P. (Ronald), Uitterlinden, A.G. (André), Hofman, A. (Albert), Alizadeh, B.Z. (Behrooz), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Ligthart, S. (Symen), Vaez, A. (Ahmad), Hsu, Y.-H. (Yi-Hsiang), Stolk, R.P. (Ronald), Uitterlinden, A.G. (André), Hofman, A. (Albert), Alizadeh, B.Z. (Behrooz), Franco, O.H. (Oscar), and Dehghan, A. (Abbas)
Abstract: Background: Genome-wide association studies (GWAS) have identified multiple genetic loci for C-reactive protein (CRP) and lipids, of which some overlap. We aimed to identify genetic pleiotropy among CRP and lipids in order to better understand the shared biology of chronic inflammation and lipid metabolism. Results: In a bivariate GWAS, we combined summary statistics of published GWAS on CRP (n = 66,185) and lipids, including LDL-cholesterol, HDL-cholesterol, triglycerides, and total cholesterol (n = 100,184), using an empirical weighted linear-combined test statistic. We sought replication for novel CRP associations in an independent sample of 17,743 genotyped individuals, and performed in silico replication of novel lipid variants in 93,982 individuals. Fifty potentially pleiotropic SNPs were identified among CRP and lipids: 21 for LDL-cholesterol and CRP, 20 for HDL-cholesterol and CRP, 21 for triglycerides, and CRP and 20 for total cholesterol and CRP. We identified and significantly replicated three novel SNPs for CRP in or near CTSB/FDFT1 (rs10435719, Preplication: 2.6 × 10-5), STAG1/PCCB (rs7621025, Preplication: 1.4 × 10-3) and FTO (rs1558902, Preplication: 2.7 × 10-5). Seven pleiotropic lipid loci were replicated in the independent set of MetaboChip samples of the Global Lipids Genetics Consortium. Annotating the effect of replicated CRP SNPs to the expression of nearby genes, we observed an effect of rs10435719 on gene expression of FDFT1, and an effect of rs7621025 on PCCB. Conclusions: Our large scale combined GWAS analysis identified numerous pleiotropic loci for CRP and lipids providing further insight in the genetic interrelation between lipids and inflammation. In addition, we provide evidence for FDFT1, PCCB and FTO to be associated with CRP levels.
Published: 2016
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14. Tobacco smoking is associated with DNA methylation of diabetes susceptibility genes

Author: Ligthart, S. (Symen), Steenaard, R.V. (Rebecca), Peters, M.J. (Marjolein), Meurs, J.B.J. (Joyce) van, Sijbrands, E.J.G. (Eric), Uitterlinden, A.G. (André), Bonder, M.J. (Marc), Hofman, A. (Albert), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Ligthart, S. (Symen), Steenaard, R.V. (Rebecca), Peters, M.J. (Marjolein), Meurs, J.B.J. (Joyce) van, Sijbrands, E.J.G. (Eric), Uitterlinden, A.G. (André), Bonder, M.J. (Marc), Hofman, A. (Albert), Franco, O.H. (Oscar), and Dehghan, A. (Abbas)
Abstract: Aims/hypothesis: Tobacco smoking, a risk factor for diabetes, is an established modifier of DNA methylation. We hypothesised that tobacco smoking modifies DNA methylation of genes previously identified for diabetes. Methods: We annotated CpG sites available on the Illumina Human Methylation 450K array to diabetes genes previously identified by genome-wide association studies (GWAS), and investigated them for an association with smoking by comparing current to never smokers. The discovery study consisted of 630 individuals (Bonferroni-corrected p = 1.4 × 10−5), and we sought replication in an independent sample of 674 individuals. The replicated sites were tested for association with nearby genetic variants and gene expression and fasting glucose and insulin levels. Results: We annotated 3,620 CpG sites to the genes identified in the GWAS on type 2 diabetes. Comparing current smokers to never smokers, we found 12 differentially methylated CpG sites, of which five replicated: cg23161492 within ANPEP (p = 1.3 × 10−12); cg26963277 (p = 1.2 × 10−9), cg01744331 (p = 8.0 × 10−6) and cg16556677 (p = 1.2 × 10−5) within KCNQ1 and cg03450842 (p = 3.1 × 10−8) within ZMIZ1. The effect of smoking on DNA methylation at the replicated CpG sites attenuated after smoking cessation. Increased DNA methylation at cg23161492 was associated with decreased gene expression levels of ANPEP (p = 8.9 × 10−5). rs231356-T, which was associated with hypomethylation of cg26963277 (KCNQ1), was associated with a higher odds of diabetes (OR 1.06, p = 1.3 × 10−5). Additionally, hypomethylation of cg26963277 was associated with lower fasting insulin levels (p = 0.0
Published: 2016
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15. DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

Author: Ligthart, S. (Symen), Marzi, C. (Carola), Aslibekyan, S. (Stella), Mendelson, M.M. (Michael M.), Conneely, K.N. (Karen N.), Tanaka, T. (Toshiko), Colicino, E. (Elena), Waite, L. (Lindsay), Joehanes, R. (Roby), Guan, W. (Weihua), Brody, J.A. (Jennifer A.), Elks, C.E. (Cathy), Marioni, R.E. (Riccardo), Jhun, M.A. (Min A.), Agha, G. (Golareh), Bressler, J. (Jan), Ward-Caviness, C.K. (Cavin K.), Chen, B.H. (Brian), Huan, T. (Tianxiao), Bakulski, K.M. (Kelly M.), Salfati, E. (Elias), Fiorito, G. (Giovanni), Wahl, S. (Simone), Schramm, K. (Katharina), Sha, J. (Jin), Hernandez, D.G. (Dena), Just, A.C. (Allan C.), Smith, J.A. (Jennifer A), Sotoodehnia, N. (Nona), Pilling, L.C. (Luke), Pankow, J.S. (James), Tsao, P.S. (Phil S.), Liu, C. (Chunyu), Zhao, W. (Wei), Guarrera, S. (Simonetta), Michopoulos, V.J. (Vasiliki J.), Smith, A.K. (Alicia K.), Peters, M.J. (Marjolein), Melzer, D. (David), Vokonas, P. (Pantel), Fornage, M. (Myriam), Prokisch, H. (Holger), Bis, J.C. (Joshua), Chu, A.Y. (Audrey), Herder, C. (Christian), Grallert, H. (Harald), Yao, C. (Chen), Shah, S. (Sonia), McRae, A.F. (Allan F.), Lin, H., Horvath, S. (Steve), Fallin, D. (Daniele), Hofman, A. (Albert), Wareham, N.J. (Nick), Wiggins, K.L. (Kerri), Feinberg, A.P. (Andrew P.), Starr, J.M. (John), Visscher, P.M. (Peter), Murabito, J. (Joanne), Kardia, S.L.R. (Sharon L.R.), Absher, D. (Devin), Binder, E.B. (Elisabeth), Singleton, A. (Andrew), Bandinelli, S. (Stefania), Peters, A. (Annette), Waldenberger, M. (Melanie), Matullo, G., Schwartz, J.D. (Joel D.), Demerath, E.W. (Ellen), Uitterlinden, A.G. (André), Meurs, J.B.J. (Joyce B.J.), Franco, O.H. (Oscar), Chen, Y.D. (Y.), Levy, D. (Daniel), Turner, S.T. (Stephen), Deary, I.J. (Ian), Ressler, K.J. (Kerry), Dupuis, J. (Josée), Ferrucci, L. (Luigi), Ong, K.K. (Ken K.), Assimes, T.L. (Themistocles), Boerwinkle, E.A. (Eric), Koenig, W. (Wolfgang), Arnett, D.K. (Donna), Baccarelli, A.A. (Andrea), Benjamin, E.J. (Emelia), Dehghan, A. (Abbas), Ligthart, S. (Symen), Marzi, C. (Carola), Aslibekyan, S. (Stella), Mendelson, M.M. (Michael M.), Conneely, K.N. (Karen N.), Tanaka, T. (Toshiko), Colicino, E. (Elena), Waite, L. (Lindsay), Joehanes, R. (Roby), Guan, W. (Weihua), Brody, J.A. (Jennifer A.), Elks, C.E. (Cathy), Marioni, R.E. (Riccardo), Jhun, M.A. (Min A.), Agha, G. (Golareh), Bressler, J. (Jan), Ward-Caviness, C.K. (Cavin K.), Chen, B.H. (Brian), Huan, T. (Tianxiao), Bakulski, K.M. (Kelly M.), Salfati, E. (Elias), Fiorito, G. (Giovanni), Wahl, S. (Simone), Schramm, K. (Katharina), Sha, J. (Jin), Hernandez, D.G. (Dena), Just, A.C. (Allan C.), Smith, J.A. (Jennifer A), Sotoodehnia, N. (Nona), Pilling, L.C. (Luke), Pankow, J.S. (James), Tsao, P.S. (Phil S.), Liu, C. (Chunyu), Zhao, W. (Wei), Guarrera, S. (Simonetta), Michopoulos, V.J. (Vasiliki J.), Smith, A.K. (Alicia K.), Peters, M.J. (Marjolein), Melzer, D. (David), Vokonas, P. (Pantel), Fornage, M. (Myriam), Prokisch, H. (Holger), Bis, J.C. (Joshua), Chu, A.Y. (Audrey), Herder, C. (Christian), Grallert, H. (Harald), Yao, C. (Chen), Shah, S. (Sonia), McRae, A.F. (Allan F.), Lin, H., Horvath, S. (Steve), Fallin, D. (Daniele), Hofman, A. (Albert), Wareham, N.J. (Nick), Wiggins, K.L. (Kerri), Feinberg, A.P. (Andrew P.), Starr, J.M. (John), Visscher, P.M. (Peter), Murabito, J. (Joanne), Kardia, S.L.R. (Sharon L.R.), Absher, D. (Devin), Binder, E.B. (Elisabeth), Singleton, A. (Andrew), Bandinelli, S. (Stefania), Peters, A. (Annette), Waldenberger, M. (Melanie), Matullo, G., Schwartz, J.D. (Joel D.), Demerath, E.W. (Ellen), Uitterlinden, A.G. (André), Meurs, J.B.J. (Joyce B.J.), Franco, O.H. (Oscar), Chen, Y.D. (Y.), Levy, D. (Daniel), Turner, S.T. (Stephen), Deary, I.J. (Ian), Ressler, K.J. (Kerry), Dupuis, J. (Josée), Ferrucci, L. (Luigi), Ong, K.K. (Ken K.), Assimes, T.L. (Themistocles), Boerwinkle, E.A. (Eric), Koenig, W. (Wolfgang), Arnett, D.K. (Donna), Baccarelli, A.A. (Andrea), Benjamin, E.J. (Emelia), and Dehghan, A. (Abbas)
Abstract: Background: Chronic low-grade inflammation reflects a subclinical immune response implicated in the pathogenesis of complex diseases. Identifying genetic loci where DNA methylation is as
Published: 2016
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16. Thyroid function and risk of type 2 diabetes: A population-based prospective cohort study

Author: Chaker, L. (Layal), Ligthart, S. (Symen), Korevaar, T.I.M. (Tim), Hofman, A. (Albert), Franco, O.H. (Oscar), Peeters, R.P. (Robin), Dehghan, A. (Abbas), Chaker, L. (Layal), Ligthart, S. (Symen), Korevaar, T.I.M. (Tim), Hofman, A. (Albert), Franco, O.H. (Oscar), Peeters, R.P. (Robin), and Dehghan, A. (Abbas)
Abstract: __Background:__ The association of thyroid function with risk of type 2 diabetes remains elusive. We aimed to investigate the association of thyroid function with incident diabetes and progression from prediabetes to diabetes in a population-based prospective cohort study. __Methods:__ We included 8452 participants (mean age 65 years) with thyroid function measurement, defined by thyroid-stimulating hormone (TSH) and free thyroxine (FT4), and longitudinal assessment of diabetes incidence. Cox-models were used to investigate the association of TSH and FT4 with diabetes and progression from prediabetes to diabetes. Multivariable models were adjusted for age, sex, high-density lipoprotein cholesterol, and glucose at
Published: 2016
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17. Maternal plasma folate impacts differential DNA methylation in an epigenome-wide meta-analysis of newborns

Author: Joubert, B.R. (Bonnie), Dekker, H.T. (Herman) den, Felix, J.F. (Janine), Bohlin, J. (Jon), Ligthart, S. (Symen), Beckett, E. (Emma), Tiemeier, H.W. (Henning), Meurs, J.B.J. (Joyce) van, Uitterlinden, A.G. (André), Hofman, A. (Albert), Håberg, S.E. (Siri E), Reese, S.E. (Sarah E.), Peters, M.J. (Marjolein), Kulle Andreassen, B. (Bettina), Steegers, E.A.P. (Eric), Nilsen, R.M. (Roy M.), Vollset, S.E. (Stein E.), Midttun, . (Øivind), Ueland, P.M. (Per), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Jongste, J.C. (Johan) de, Wu, M.C. (Michael), Wang, T. (Tianyuan), Peddada, S.D. (Shyamal D.), Jaddoe, V.W.V. (Vincent), Nystad, W. (Wenche), Duijts, L. (Liesbeth), London, S.J. (Stephanie J), Joubert, B.R. (Bonnie), Dekker, H.T. (Herman) den, Felix, J.F. (Janine), Bohlin, J. (Jon), Ligthart, S. (Symen), Beckett, E. (Emma), Tiemeier, H.W. (Henning), Meurs, J.B.J. (Joyce) van, Uitterlinden, A.G. (André), Hofman, A. (Albert), Håberg, S.E. (Siri E), Reese, S.E. (Sarah E.), Peters, M.J. (Marjolein), Kulle Andreassen, B. (Bettina), Steegers, E.A.P. (Eric), Nilsen, R.M. (Roy M.), Vollset, S.E. (Stein E.), Midttun, . (Øivind), Ueland, P.M. (Per), Franco, O.H. (Oscar), Dehghan, A. (Abbas), Jongste, J.C. (Johan) de, Wu, M.C. (Michael), Wang, T. (Tianyuan), Peddada, S.D. (Shyamal D.), Jaddoe, V.W.V. (Vincent), Nystad, W. (Wenche), Duijts, L. (Liesbeth), and London, S.J. (Stephanie J)
Abstract: Folate is vital for fetal development. Periconceptional folic acid supplementation and food fortification are recommended to prevent neural tube defects. Mechanisms whereby periconceptional folate influences normal development and disease are poorly understood: epigenetics may be involved. We examine the association between maternal plasma folate during pregnancy and epigenome-wide DNA methylation using Illumina" s HumanMethyl450 Beadchip in 1,988 newborns from two European cohorts. Here we report the combined covariate-adjusted results using meta-analysis and employ pathway and gene expression analyses. Four-hundred forty-three CpGs (320 genes) are significantly associated with maternal plasma folate levels during pregnancy (false discovery rate 5%); 48 are significant after Bonferroni correction. Most genes are not known for folate biology, including APC2, GRM8, SLC16A12, OPCML, PRPH, LHX1, KLK4 and PRSS21. Some relate to birth defects other than neural tube defects, neurological functions or varied aspects of embryonic development. These findings may inform how maternal folate impacts the developing epigenome and health outcomes in offspring.
Published: 2016
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18. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis

Author: Joubert, B.R. (Bonnie), Felix, J.F. (Janine), Yousefi, P. (Paul), Bakulski, K.M. (Kelly M.), Just, A.C. (Allan C.), Breton, C. (Carrie), Reese, S.E. (Sarah E.), Markunas, C.A. (Christina A.), Richmond, R.C. (Rebecca C.), Xu, C.-J. (Cheng-Jian), Küpers, L.K. (Leanne), Oh, S.S. (Sam S.), Hoyo, C. (Cathrine), Gruzieva, O. (Olena), Söderhäll, C. (Cilla), Salas, L.A. (Lucas A.), Baïz, N. (Nour), Zhang, H. (Hongmei), Lepeule, J. (Johanna), Ruiz, C. (Carlos), Ligthart, S. (Symen), Wang, T. (Tianyuan), Taylor, J.A. (Jack A.), Duijts, L. (Liesbeth), Sharp, G.C. (Gemma C.), Jankipersadsing, S.A. (Soesma A.), Nilsen, R.M. (Roy M.), Vaez, A. (Ahmad), Fallin, M.D. (M. Daniele), Hu, D. (Donglei), Litonjua, A.A. (Augusto), Fuemmeler, B.F. (Bernard F.), Huen, K. (Karen), Kere, J. (Juha), Kull, C.A. (Christian), Munthe-Kaas, M.C. (Monica Cheng), Gehring, U. (Ulrike), Bustamante, M. (Mariona), Saurel-Coubizolles, M.J. (Marie José), Quraishi, B.M. (Bilal M.), Ren, J. (Jie), Tost, J. (Jörg), Gonzalez, J.R. (Juan R.), Peters, M.J. (Marjolein), Håberg, S.E. (Siri E), Xu, Z. (Zongli), Meurs, J.B.J. (Joyce) van, Gaunt, T.R. (Tom), Kerkhof, M. (Marjan), Corpeleijn, W.E. (Willemijn), Feinberg, A.P. (Andrew P.), Eng, C. (Celeste), Baccarelli, A.A. (Andrea), Benjamin Neelon, S.E. (Sara E.), Bradman, A. (Asa), Merid, S.K. (Simon Kebede), Bergström, A. (Anna), Herceg, Z. (Zdenko), Hernandez-Vargas, H. (Hector), Brunekreef, B. (Bert), Pinart, M. (Mariona), Heude, B. (Barbara), Ewart, S. (Susan), Yao, J. (Jin), Lemonnier, N. (Nathanaël), Franco, O.H. (Oscar), Wu, M.C. (Michael), Hofman, A. (Albert), McArdle, W.L. (Wendy), Vlies, P. (P.) van der, Falahi, F. (Fahimeh), Gillman, M.W. (Matthew W.), Barcellos, L.F. (Lisa), Kumar, A. (Ashish), Wickman, M. (Magnus), Guerra, S. (S.), Charles, M.-A. (Marie-Aline), Holloway, J. (John), Auffray, C. (C.), Tiemeier, H.W. (Henning), Smith, A.V. (Davey), Postma, D.S. (Dirkje), Hivert, M.-F. (Marie-France), Eskenazi, B. (Brenda), Vrijheid, M. (Martine), Arshad, H. (Hasan), Anto, J.M. (Josep), Dehghan, A. (Abbas), Karmaus, W. (Wilfried), Annesi-Maesano, I. (Isabella), Sunyer, J. (Jordi), Ghantous, A. (Akram), Pershagen, G. (Göran), Holland, N. (Nina), Murphy, S.K. (Susan K.), Demeo, D.L. (Dawn), Burchard, E.G. (Esteban), Ladd-Acosta, C. (Christine), Snieder, H. (Harold), Nystad, W. (Wenche), Koppelman, G.H. (Gerard), Relton, C.L. (Caroline), Jaddoe, V.W.V. (Vincent), Wilcox, A.J. (Allen), Melén, E. (Erik), London, S.J. (Stephanie J.), Joubert, B.R. (Bonnie), Felix, J.F. (Janine), Yousefi, P. (Paul), Bakulski, K.M. (Kelly M.), Just, A.C. (Allan C.), Breton, C. (Carrie), Reese, S.E. (Sarah E.), Markunas, C.A. (Christina A.), Richmond, R.C. (Rebecca C.), Xu, C.-J. (Cheng-Jian), Küpers, L.K. (Leanne), Oh, S.S. (Sam S.), Hoyo, C. (Cathrine), Gruzieva, O. (Olena), Söderhäll, C. (Cilla), Salas, L.A. (Lucas A.), Baïz, N. (Nour), Zhang, H. (Hongmei), Lepeule, J. (Johanna), Ruiz, C. (Carlos), Ligthart, S. (Symen), Wang, T. (Tianyuan), Taylor, J.A. (Jack A.), Duijts, L. (Liesbeth), Sharp, G.C. (Gemma C.), Jankipersadsing, S.A. (Soesma A.), Nilsen, R.M. (Roy M.), Vaez, A. (Ahmad), Fallin, M.D. (M. Daniele), Hu, D. (Donglei), Litonjua, A.A. (Augusto), Fuemmeler, B.F. (Bernard F.), Huen, K. (Karen), Kere, J. (Juha), Kull, C.A. (Christian), Munthe-Kaas, M.C. (Monica Cheng), Gehring, U. (Ulrike), Bustamante, M. (Mariona), Saurel-Coubizolles, M.J. (Marie José), Quraishi, B.M. (Bilal M.), Ren, J. (Jie), Tost, J. (Jörg), Gonzalez, J.R. (Juan R.), Peters, M.J. (Marjolein), Håberg, S.E. (Siri E), Xu, Z. (Zongli), Meurs, J.B.J. (Joyce) van, Gaunt, T.R. (Tom), Kerkhof, M. (Marjan), Corpeleijn, W.E. (Willemijn), Feinberg, A.P. (Andrew P.), Eng, C. (Celeste), Baccarelli, A.A. (Andrea), Benjamin Neelon, S.E. (Sara E.), Bradman, A. (Asa), Merid, S.K. (Simon Kebede), Bergström, A. (Anna), Herceg, Z. (Zdenko), Hernandez-Vargas, H. (Hector), Brunekreef, B. (Bert), Pinart, M. (Mariona), Heude, B. (Barbara), Ewart, S. (Susan), Yao, J. (Jin), Lemonnier, N. (Nathanaël), Franco, O.H. (Oscar), Wu, M.C. (Michael), Hofman, A. (Albert), McArdle, W.L. (Wendy), Vlies, P. (P.) van der, Falahi, F. (Fahimeh), Gillman, M.W. (Matthew W.), Barcellos, L.F. (Lisa), Kumar, A. (Ashish), Wickman, M. (Magnus), Guerra, S. (S.), Charles, M.-A. (Marie-Aline), Holloway, J. (John), Auffray, C. (C.), Tiemeier, H.W. (Henning), Smith, A.V. (Davey), Postma, D.S. (Dirkje), Hivert, M.-F. (Marie-France), Eskenazi, B. (Brenda), Vrijheid, M. (Martine), Arshad, H. (Hasan), Anto, J.M. (Josep), Dehghan, A. (Abbas), Karmaus, W. (Wilfried), Annesi-Maesano, I. (Isabella), Sunyer, J. (Jordi), Ghantous, A. (Akram), Pershagen, G. (Göran), Holland, N. (Nina), Murphy, S.K. (Susan K.), Demeo, D.L. (Dawn), Burchard, E.G. (Esteban), Ladd-Acosta, C. (Christine), Snieder, H. (Harold), Nystad, W. (Wenche), Koppelman, G.H. (Gerard), Relton, C.L. (Caroline), Jaddoe, V.W.V. (Vincent), Wilcox, A.J. (Allen), Melén, E. (Erik), and London, S.J. (Stephanie J.)
Abstract: Epigenetic modifications, including DNA methylation, represent a potential mechanism for environmental impacts on human disease. Maternal smoking in pregnancy remains an important public health problem that impacts child health in a myriad of ways and has potential lifelong consequences. The mechanisms are largely unknown, but epigenetics most likely plays a role. We formed the Pregnancy And Childhood Epigenetics (PACE) consortium and meta-analyzed, across 13 cohorts (n = 6,685), the association between maternal smoking in pregnancy and newborn blood DNA methylation at over 450,000 CpG sites (CpGs) by using the Illumina 450K BeadChip. Over 6,000 CpGs were differentially methylated in relation to maternal smoking at genome-wide statistical significance (false discovery rate, 5%), including 2,965 CpGs corresponding to 2,017 genes not previously related to smoking and methylation in either newborns or adults. Several genes are relevant to diseases that can be caused by maternal smoking (e.g., orofacial clefts and asthma) or adult smoking (e.g., certain cancers). A number of differentially methylated CpGs were associated with gene expression. We observed enrichment in pathwa
Published: 2016
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19. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

Author: Ligthart, S. (Symen), Vries, P.S. (Paul) de, Uitterlinden, A.G. (André), Hofman, A. (Albert), Franco, O.H. (Oscar), Chasman, D.I. (Daniel), Dehghan, A. (Abbas), Dupuis, J. (Josée), Barbalic, M. (maja), Bis, J.C. (Joshua), Eiriksdottir, G. (Gudny), Lu, C. (Chen), Pellikka, N. (Niina), Wallaschofski, H. (Henri), Kettunen, J. (Johannes), Henneman, P. (Peter), Baumert, J. (Jens), Strachan, D.P. (David), Fuchsberger, C. (Christian), Vitart, V. (Veronique), Wilson, J.F. (James F), Paré, G. (Guillaume), Naitza, S. (Silvia), Rudock, M.E. (Megan), Surakka, I. (Ida), Geus, E.J.C. (Eco) de, Alizadeh, B.Z. (Behrooz), Guralnik, J.M. (Jack), Shuldiner, A.R. (Alan), Tanaka, T. (Toshiko), Zee, R.Y.L. (Robert), Schnabel, R.B. (Renate), Nambi, V. (Vijay), Kavousi, M. (Maryam), Ripatti, S. (Samuli), Nauck, M. (Matthias), Smith, N.L. (Nicholas L.), Smith, A.V. (Albert Vernon), Sundvall, J. (Jouko), Scheet, P. (Paul), Liu, Y. (YongMei), Ruokonen, A. (Aimo), Rose, L.M. (Lynda), Larson, M.G. (Martin), Hoogeveen, R.C. (Ron), Freimer, N.B. (Nelson), Teumer, A. (Alexander), Tracy, R.P. (Russell), Launer, L.J. (Lenore), Buring, J.E. (Julie), Yamamoto, J.F. (Jennifer), Folsom, A.R. (Aaron), Sijbrands, E.J.G. (Eric), Pankow, J.S. (James), Elliott, P. (Paul), Keaney, J.F. (John), Sun, W. (Wei), Sarin, A.-P., Fontes, M. (Michel), Badola, S. (Sunita), Astor, B.C. (Brad), Pouta, A. (Anneli), Werda, K. (Karl), Greiser, K.H. (Karin Halina), Kuss, O. (Oliver), Schwabedissen, H.E.M.Z. (Henriette E. Meyer Zu), Thiery, J. (Joachim), Jamshidi, Y. (Yalda), Nolte, I.M. (Ilja M.), Soranzo, N. (Nicole), Spector, T.D. (Timothy), Völzke, H. (Henry), Parker, A.N. (Alex), Aspelund, T. (Thor), Bates, D. (David), Young, L. (Lauren), Tsui, K. (Kim), Siscovick, D.S. (David), Guo, X. (Xiuqing), Rotter, J.I. (Jerome I.), Uda, M. (Manuela), Schlessinger, D., Rudan, I. (Igor), Hicks, A.A. (Andrew), Penninx, B.W.J.H. (Brenda), Thorand, B. (Barbara), Gieger, C. (Christian), Coresh, J. (Josef), Willemsen, G.A.H.M. (Gonneke), Harris, T.B. (Tamara), Jarvelin, M.-R. (Marjo-Riitta), Rice, K.M. (Kenneth), Radke, D. (Dörte), Salomaa, V. (Veikko), Willems van Dijk, J.A.P. (Ko), Boerwinkle, E.A. (Eric), Vasan, R.S. (Ramachandran Srini), Ferrucci, L. (Luigi), Gibson, Q. (Quince), Bandinelli, S. (Stefania), Snieder, H. (Harold), Boomsma, D.I. (Dorret), Xiao, X. (Xiangjun), Campbell, H. (Harry), Hayward, C. (Caroline), Pramstaller, P.P. (Peter Paul), Duijn, C.M. (Cornelia) van, Peltonen, L. (Leena Johanna), Psaty, B.M. (Bruce), Gudnason, V. (Vilmundur), Ridker, P.M. (Paul), Homuth, G. (Georg), Koenig, W. (Wolfgang), Ballantyne, C. (Christie), Witteman, J.C.M. (Jacqueline), Benjamin, E.J. (Emelia), Perola, M. (Markus), Chasman., D.I. (Daniel I.), Ligthart, S. (Symen), Vries, P.S. (Paul) de, Uitterlinden, A.G. (André), Hofman, A. (Albert), Franco, O.H. (Oscar), Chasman, D.I. (Daniel), Dehghan, A. (Abbas), Dupuis, J. (Josée), Barbalic, M. (maja), Bis, J.C. (Joshua), Eiriksdottir, G. (Gudny), Lu, C. (Chen), Pellikka, N. (Niina), Wallaschofski, H. (Henri), Kettunen, J. (Johannes), Henneman, P. (Peter), Baumert, J. (Jens), Strachan, D.P. (David), Fuchsberger, C. (Christian), Vitart, V. (Veronique), Wilson, J.F. (James F), Paré, G. (Guillaume), Naitza, S. (Silvia), Rudock, M.E. (Megan), Surakka, I. (Ida), Geus, E.J.C. (Eco) de, Alizadeh, B.Z. (Behrooz), Guralnik, J.M. (Jack), Shuldiner, A.R. (Alan), Tanaka, T. (Toshiko), Zee, R.Y.L. (Robert), Schnabel, R.B. (Renate), Nambi, V. (Vijay), Kavousi, M. (Maryam), Ripatti, S. (Samuli), Nauck, M. (Matthias), Smith, N.L. (Nicholas L.), Smith, A.V. (Albert Vernon), Sundvall, J. (Jouko), Scheet, P. (Paul), Liu, Y. (YongMei), Ruokonen, A. (Aimo), Rose, L.M. (Lynda), Larson, M.G. (Martin), Hoogeveen, R.C. (Ron), Freimer, N.B. (Nelson), Teumer, A. (Alexander), Tracy, R.P. (Russell), Launer, L.J. (Lenore), Buring, J.E. (Julie), Yamamoto, J.F. (Jennifer), Folsom, A.R. (Aaron), Sijbrands, E.J.G. (Eric), Pankow, J.S. (James), Elliott, P. (Paul), Keaney, J.F. (John), Sun, W. (Wei), Sarin, A.-P., Fontes, M. (Michel), Badola, S. (Sunita), Astor, B.C. (Brad), Pouta, A. (Anneli), Werda, K. (Karl), Greiser, K.H. (Karin Halina), Kuss, O. (Oliver), Schwabedissen, H.E.M.Z. (Henriette E. Meyer Zu), Thiery, J. (Joachim), Jamshidi, Y. (Yalda), Nolte, I.M. (Ilja M.), Soranzo, N. (Nicole), Spector, T.D. (Timothy), Völzke, H. (Henry), Parker, A.N. (Alex), Aspelund, T. (Thor), Bates, D. (David), Young, L. (Lauren), Tsui, K. (Kim), Siscovick, D.S. (David), Guo, X. (Xiuqing), Rotter, J.I. (Jerome I.), Uda, M. (Manuela), Schlessinger, D., Rudan, I. (Igor), Hicks, A.A. (Andrew), Penninx, B.W.J.H. (Brenda), Thorand, B. (Barbara), Gieger, C. (Christian), Coresh, J. (Josef), Willemsen, G.A.H.M. (Gonneke), Harris, T.B. (Tamara), Jarvelin, M.-R. (Marjo-Riitta), Rice, K.M. (Kenneth), Radke, D. (Dörte), Salomaa, V. (Veikko), Willems van Dijk, J.A.P. (Ko), Boerwinkle, E.A. (Eric), Vasan, R.S. (Ramachandran Srini), Ferrucci, L. (Luigi), Gibson, Q. (Quince), Bandinelli, S. (Stefania), Snieder, H. (Harold), Boomsma, D.I. (Dorret), Xiao, X. (Xiangjun), Campbell, H. (Harry), Hayward, C. (Caroline), Pramstaller, P.P. (Peter Paul), Duijn, C.M. (Cornelia) van, Peltonen, L. (Leena Johanna), Psaty, B.M. (Bruce), Gudnason, V. (Vilmundur), Ridker, P.M. (Paul), Homuth, G. (Georg), Koenig, W. (Wolfgang), Ballantyne, C. (Christie), Witteman, J.C.M. (Jacqueline), Benjamin, E.J. (Emelia), Perola, M. (Markus), and Chasman., D.I. (Daniel I.)
Abstract: Pleiotropic genetic variants have independent effects on different phenotypes. C-reactive protein (CRP) is associated with several cardiometabolic phenotypes. Shared genetic backgrounds may partially underlie these associations. We conducted a genome-wide analysis to identify the shared genetic background of inflammation and cardiometabolic phenotypes using published genome-wide association studies (GWAS). We also evaluated whether the pleiotropic effects of such loci were biological or mediated in nature. First, we examined whether 283 common variants identified for 10 cardiometabolic phenotypes in GWAS are associated with CRP level. Second, we tested whether 18 variants identified for serum CRP are associated with 10 cardiometabolic phenotypes. We used a Bonferroni corrected p-value of 1.1×10-04 (0.05/463) as a threshold of significance. We evaluated the independent pleiotropic effect on both phenotypes using individual level data from the Women Genome Health Study. Evaluating the genetic overlap between inflammation and cardiometabolic phenotypes, we found 13 pleiotropic regions. Additional analyses showed that 6 regions (APOC1, HNF1A, IL6R, PPP1R3B, HNF4A and IL1F10) appeared to have a pleiotropic effect on CRP independent of the effects on the cardiometabolic phenotypes. These included loci where individuals carrying the risk allele for CRP encounter higher lipid levels and risk of type 2 diabetes. In addition, 5 regions (GCKR, PABPC4, BCL7B, FTO and TMEM18) had an effect on CRP largely mediated through the cardiometabolic phenotypes. In conclusion, our results show genetic pleiotropy among inflammation and cardiometabolic phenotypes. In addition to reverse causation, our data suggests that pleiotropic genetic variants partially underlie the association between CRP and cardiometabolic phenotypes.
Published: 2015
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20. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

Author: Ligthart, S. (Symen), Vries, P.S. (Paul) de, Uitterlinden, A.G. (André), Hofman, A. (Albert), Franco, O.H. (Oscar), Chasman, D.I. (Daniel), Dehghan, A. (Abbas), Dupuis, J. (Josée), Barbalic, M. (maja), Bis, J.C. (Joshua), Eiriksdottir, G. (Gudny), Lu, C. (Chen), Pellikka, N. (Niina), Wallaschofski, H. (Henri), Kettunen, J. (Johannes), Henneman, P. (Peter), Baumert, J. (Jens), Strachan, D.P. (David), Fuchsberger, C. (Christian), Vitart, V. (Veronique), Wilson, J.F. (James F), Paré, G. (Guillaume), Naitza, S. (Silvia), Rudock, M.E. (Megan), Surakka, I. (Ida), Geus, E.J.C. (Eco) de, Alizadeh, B.Z. (Behrooz), Guralnik, J.M. (Jack), Shuldiner, A.R. (Alan), Tanaka, T. (Toshiko), Zee, R.Y.L. (Robert), Schnabel, R.B. (Renate), Nambi, V. (Vijay), Kavousi, M. (Maryam), Ripatti, S. (Samuli), Nauck, M. (Matthias), Smith, N.L. (Nicholas L.), Smith, A.V. (Albert Vernon), Sundvall, J. (Jouko), Scheet, P. (Paul), Liu, Y. (YongMei), Ruokonen, A. (Aimo), Rose, L.M. (Lynda), Larson, M.G. (Martin), Hoogeveen, R.C. (Ron), Freimer, N.B. (Nelson), Teumer, A. (Alexander), Tracy, R.P. (Russell), Launer, L.J. (Lenore), Buring, J.E. (Julie), Yamamoto, J.F. (Jennifer), Folsom, A.R. (Aaron), Sijbrands, E.J.G. (Eric), Pankow, J.S. (James), Elliott, P. (Paul), Keaney, J.F. (John), Sun, W. (Wei), Sarin, A.-P., Fontes, M. (Michel), Badola, S. (Sunita), Astor, B.C. (Brad), Pouta, A. (Anneli), Werda, K. (Karl), Greiser, K.H. (Karin Halina), Kuss, O. (Oliver), Schwabedissen, H.E.M.Z. (Henriette E. Meyer Zu), Thiery, J. (Joachim), Jamshidi, Y. (Yalda), Nolte, I.M. (Ilja M.), Soranzo, N. (Nicole), Spector, T.D. (Timothy), Völzke, H. (Henry), Parker, A.N. (Alex), Aspelund, T. (Thor), Bates, D. (David), Young, L. (Lauren), Tsui, K. (Kim), Siscovick, D.S. (David), Guo, X. (Xiuqing), Rotter, J.I. (Jerome I.), Uda, M. (Manuela), Schlessinger, D., Rudan, I. (Igor), Hicks, A.A. (Andrew), Penninx, B.W.J.H. (Brenda), Thorand, B. (Barbara), Gieger, C. (Christian), Coresh, J. (Josef), Willemsen, G.A.H.M. (Gonneke), Harris, T.B. (Tamara), Jarvelin, M.-R. (Marjo-Riitta), Rice, K.M. (Kenneth), Radke, D. (Dörte), Salomaa, V. (Veikko), Willems van Dijk, J.A.P. (Ko), Boerwinkle, E.A. (Eric), Vasan, R.S. (Ramachandran Srini), Ferrucci, L. (Luigi), Gibson, Q. (Quince), Bandinelli, S. (Stefania), Snieder, H. (Harold), Boomsma, D.I. (Dorret), Xiao, X. (Xiangjun), Campbell, H. (Harry), Hayward, C. (Caroline), Pramstaller, P.P. (Peter Paul), Duijn, C.M. (Cornelia) van, Peltonen, L. (Leena Johanna), Psaty, B.M. (Bruce), Gudnason, V. (Vilmundur), Ridker, P.M. (Paul), Homuth, G. (Georg), Koenig, W. (Wolfgang), Ballantyne, C. (Christie), Witteman, J.C.M. (Jacqueline), Benjamin, E.J. (Emelia), Perola, M. (Markus), Chasman., D.I. (Daniel I.), Ligthart, S. (Symen), Vries, P.S. (Paul) de, Uitterlinden, A.G. (André), Hofman, A. (Albert), Franco, O.H. (Oscar), Chasman, D.I. (Daniel), Dehghan, A. (Abbas), Dupuis, J. (Josée), Barbalic, M. (maja), Bis, J.C. (Joshua), Eiriksdottir, G. (Gudny), Lu, C. (Chen), Pellikka, N. (Niina), Wallaschofski, H. (Henri), Kettunen, J. (Johannes), Henneman, P. (Peter), Baumert, J. (Jens), Strachan, D.P. (David), Fuchsberger, C. (Christian), Vitart, V. (Veronique), Wilson, J.F. (James F), Paré, G. (Guillaume), Naitza, S. (Silvia), Rudock, M.E. (Megan), Surakka, I. (Ida), Geus, E.J.C. (Eco) de, Alizadeh, B.Z. (Behrooz), Guralnik, J.M. (Jack), Shuldiner, A.R. (Alan), Tanaka, T. (Toshiko), Zee, R.Y.L. (Robert), Schnabel, R.B. (Renate), Nambi, V. (Vijay), Kavousi, M. (Maryam), Ripatti, S. (Samuli), Nauck, M. (Matthias), Smith, N.L. (Nicholas L.), Smith, A.V. (Albert Vernon), Sundvall, J. (Jouko), Scheet, P. (Paul), Liu, Y. (YongMei), Ruokonen, A. (Aimo), Rose, L.M. (Lynda), Larson, M.G. (Martin), Hoogeveen, R.C. (Ron), Freimer, N.B. (Nelson), Teumer, A. (Alexander), Tracy, R.P. (Russell), Launer, L.J. (Lenore), Buring, J.E. (Julie), Yamamoto, J.F. (Jennifer), Folsom, A.R. (Aaron), Sijbrands, E.J.G. (Eric), Pankow, J.S. (James), Elliott, P. (Paul), Keaney, J.F. (John), Sun, W. (Wei), Sarin, A.-P., Fontes, M. (Michel), Badola, S. (Sunita), Astor, B.C. (Brad), Pouta, A. (Anneli), Werda, K. (Karl), Greiser, K.H. (Karin Halina), Kuss, O. (Oliver), Schwabedissen, H.E.M.Z. (Henriette E. Meyer Zu), Thiery, J. (Joachim), Jamshidi, Y. (Yalda), Nolte, I.M. (Ilja M.), Soranzo, N. (Nicole), Spector, T.D. (Timothy), Völzke, H. (Henry), Parker, A.N. (Alex), Aspelund, T. (Thor), Bates, D. (David), Young, L. (Lauren), Tsui, K. (Kim), Siscovick, D.S. (David), Guo, X. (Xiuqing), Rotter, J.I. (Jerome I.), Uda, M. (Manuela), Schlessinger, D., Rudan, I. (Igor), Hicks, A.A. (Andrew), Penninx, B.W.J.H. (Brenda), Thorand, B. (Barbara), Gieger, C. (Christian), Coresh, J. (Josef), Willemsen, G.A.H.M. (Gonneke), Harris, T.B. (Tamara), Jarvelin, M.-R. (Marjo-Riitta), Rice, K.M. (Kenneth), Radke, D. (Dörte), Salomaa, V. (Veikko), Willems van Dijk, J.A.P. (Ko), Boerwinkle, E.A. (Eric), Vasan, R.S. (Ramachandran Srini), Ferrucci, L. (Luigi), Gibson, Q. (Quince), Bandinelli, S. (Stefania), Snieder, H. (Harold), Boomsma, D.I. (Dorret), Xiao, X. (Xiangjun), Campbell, H. (Harry), Hayward, C. (Caroline), Pramstaller, P.P. (Peter Paul), Duijn, C.M. (Cornelia) van, Peltonen, L. (Leena Johanna), Psaty, B.M. (Bruce), Gudnason, V. (Vilmundur), Ridker, P.M. (Paul), Homuth, G. (Georg), Koenig, W. (Wolfgang), Ballantyne, C. (Christie), Witteman, J.C.M. (Jacqueline), Benjamin, E.J. (Emelia), Perola, M. (Markus), and Chasman., D.I. (Daniel I.)
Abstract: Pleiotropic genetic variants have independent effects on different phenotypes. C-reactive protein (CRP) is associated with several cardiometabolic phenotypes. Shared genetic backgrounds may partially underlie these associations. We conducted a genome-wide analysis to identify the shared genetic background of inflammation and cardiometabolic phenotypes using published genome-wide association studies (GWAS). We also evaluated whether the pleiotropic effects of such loci were biological or mediated in nature. First, we examined whether 283 common variants identified for 10 cardiometabolic phenotypes in GWAS are associated with CRP level. Second, we tested whether 18 variants identified for serum CRP are associated with 10 cardiometabolic phenotypes. We used a Bonferroni corrected p-value of 1.1×10-04 (0.05/463) as a threshold of significance. We evaluated the independent pleiotropic effect on both phenotypes using individual level data from the Women Genome Health Study. Evaluating the genetic overlap between inflammation and cardiometabolic phenotypes, we found 13 pleiotropic regions. Additional analyses showed that 6 regions (APOC1, HNF1A, IL6R, PPP1R3B, HNF4A and IL1F10) appeared to have a pleiotropic effect on CRP independent of the effects on the cardiometabolic phenotypes. These included loci where individuals carrying the risk allele for CRP encounter higher lipid levels and risk of type 2 diabetes. In addition, 5 regions (GCKR, PABPC4, BCL7B, FTO and TMEM18) had an effect on CRP largely mediated through the cardiometabolic phenotypes. In conclusion, our results show genetic pleiotropy among inflammation and cardiometabolic phenotypes. In addition to reverse causation, our data suggests that pleiotropic genetic variants partially underlie the association between CRP and cardiometabolic phenotypes.
Published: 2015
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21. Vitamin D and C-reactive protein

Author: Liefaard, M.C. (Marte C.), Ligthart, S. (Symen), Vitezova, A. (Anna), Hofman, A. (Albert), Uitterlinden, A.G. (André), Kiefte-de Jong, J.C. (Jessica), Franco, O.H. (Oscar), Zillikens, M.C. (Carola), Dehghan, A. (Abbas), Liefaard, M.C. (Marte C.), Ligthart, S. (Symen), Vitezova, A. (Anna), Hofman, A. (Albert), Uitterlinden, A.G. (André), Kiefte-de Jong, J.C. (Jessica), Franco, O.H. (Oscar), Zillikens, M.C. (Carola), and Dehghan, A. (Abbas)
Abstract: Vitamin D deficiency is widely prevalent and has been associated with many diseases. It has been suggested that vitamin D has effects on the immune system and inhibits inflammation. The aim of our study was to investigate whether vitamin D has an inhibitory effect on systemic inflammation by assessing the association between serum levels of vitamin D and C-reactive protein. We studied the association between serum 25-hydroxyvitamin D and C-reactive protein through linear regression in 9,649 participants of the Rotterdam Study, an observational, prospective population-based cohort study. We used genetic variants related to vitamin D and CRP to compute a genetic risk score and perform bi-directional Mendelian randomization analysis. In linear regression adjusted for age, sex, cohort and other confounders, natural log-transformed CRP decreased with 0.06 (95% CI: -0.08, -0.03) unit per standard deviation increase in 25-hydroxyvitamin D. Bi-directional Mendelian randomization analyses showed no association between the vitamin D genetic risk score and lnCRP (Beta per SD = -0.018; p = 0.082) or the CRP genetic risk score and 25-hydroxyvitamin D (Beta per SD = 0.001; p = 0.998). In conclusion, higher levels of Vitamin D are associated with lower levels of C-reactive protein. In this study we did not find evidence for this to be the result of a causal relationship. Copyright
Published: 2015
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22. Pleiotropic genes for metabolic syndrome and inflammation

Author: Kraja, A. (Aldi), Chasman, D.I. (Daniel), North, K.E. (Kari), Reiner, A. (Alexander), Yanek, L.R. (Lisa), Kilpeläinen, T.O. (Tuomas), Smith, J.A. (Jennifer), Dehghan, A. (Abbas), Dupuis, J. (Josée), Johnson, A.D. (Andrew), Feitosa, M.F. (Mary Furlan), Tekola-Ayele, F. (Fasil), Chu, A.Y. (Audrey), Nolte, I.M. (Ilja), Dastani, Z. (Zari), Morris, A.P. (Andrew), Pendergrass, S.A. (Sarah), Sun, Y.V. (Yan), Ritchie, M.D. (Marylyn), Vaez, A. (Ahmad), Lin, H. (Honghuang), Ligthart, S. (Symen), Marullo, L. (Letizia), Rohde, R. (Rebecca), Shao, Y. (Yaming), Ziegler, M.A. (Mark), Im, K.M. (Kate), Schnabel, R.B. (Renate), Jorgensen, T. (Torben), Jørgensen, M.E. (Marit), Hansen, T. (T.), Pedersen, O. (Oluf), Stolk, R.P. (Ronald), Snieder, H. (Harold), Hofman, A. (Albert), Uitterlinden, A.G. (André), Franco, O.H. (Oscar), Ikram, M.A. (Arfan), Richards, J.B. (Brent), Rotimi, C. (Charles), Wilson, J.G. (James), Lange, L.A. (Leslie), Ganesh, S.K. (Santhi), Nalls, M.A. (Michael), Rasmussen-Torvik, L.J. (Laura), Pankow, J.S. (James), Coresh, J. (Josef), Tang, W. (Weihong), Kao, W.-H.L. (Linda), Boerwinkle, E.A. (Eric), Morrison, A.C. (Alanna), Ridker, P.M. (Paul), Becker, D.M. (Diane), Rotter, J.I. (Jerome), Kardia, S.L.R. (Sharon), Loos, R.J.F. (Ruth), Larson, M.G. (Martin), Hsu, Y.-H. (Yi-Hsiang), Province, M.A. (Mike), Tracy, R.P. (Russell), Voight, B.F. (Benjamin), Vaidya, D. (Dhananjay), O'Donnell, C.J. (Christopher), Benjamin, E.J. (Emelia), Alizadeh, B.Z. (Behrooz), Prokopenko, I. (Inga), Meigs, J.B. (James), Borecki, I.B. (Ingrid), Kraja, A. (Aldi), Chasman, D.I. (Daniel), North, K.E. (Kari), Reiner, A. (Alexander), Yanek, L.R. (Lisa), Kilpeläinen, T.O. (Tuomas), Smith, J.A. (Jennifer), Dehghan, A. (Abbas), Dupuis, J. (Josée), Johnson, A.D. (Andrew), Feitosa, M.F. (Mary Furlan), Tekola-Ayele, F. (Fasil), Chu, A.Y. (Audrey), Nolte, I.M. (Ilja), Dastani, Z. (Zari), Morris, A.P. (Andrew), Pendergrass, S.A. (Sarah), Sun, Y.V. (Yan), Ritchie, M.D. (Marylyn), Vaez, A. (Ahmad), Lin, H. (Honghuang), Ligthart, S. (Symen), Marullo, L. (Letizia), Rohde, R. (Rebecca), Shao, Y. (Yaming), Ziegler, M.A. (Mark), Im, K.M. (Kate), Schnabel, R.B. (Renate), Jorgensen, T. (Torben), Jørgensen, M.E. (Marit), Hansen, T. (T.), Pedersen, O. (Oluf), Stolk, R.P. (Ronald), Snieder, H. (Harold), Hofman, A. (Albert), Uitterlinden, A.G. (André), Franco, O.H. (Oscar), Ikram, M.A. (Arfan), Richards, J.B. (Brent), Rotimi, C. (Charles), Wilson, J.G. (James), Lange, L.A. (Leslie), Ganesh, S.K. (Santhi), Nalls, M.A. (Michael), Rasmussen-Torvik, L.J. (Laura), Pankow, J.S. (James), Coresh, J. (Josef), Tang, W. (Weihong), Kao, W.-H.L. (Linda), Boerwinkle, E.A. (Eric), Morrison, A.C. (Alanna), Ridker, P.M. (Paul), Becker, D.M. (Diane), Rotter, J.I. (Jerome), Kardia, S.L.R. (Sharon), Loos, R.J.F. (Ruth), Larson, M.G. (Martin), Hsu, Y.-H. (Yi-Hsiang), Province, M.A. (Mike), Tracy, R.P. (Russell), Voight, B.F. (Benjamin), Vaidya, D. (Dhananjay), O'Donnell, C.J. (Christopher), Benjamin, E.J. (Emelia), Alizadeh, B.Z. (Behrooz), Prokopenko, I. (Inga), Meigs, J.B. (James), and Borecki, I.B. (Ingrid)
Abstract: Metabolic syndrome (MetS) has become a health and financial burden worldwide. The MetS definition captures clustering of risk factors that predict higher risk for diabetes mellitus and cardiovascular disease. Our study hypothesis is that additional to genes influencing individual MetS risk factors, genetic variants exist that influence MetS and inflammatory markers forming a predisposing MetS genetic network. To test this hypothesis a staged approach was undertaken. (a) We analyzed 17 metabolic and inflammatory traits in more than 85,500 participants from 14 large epidemiological studies within the Cross Consortia Pleiotropy Group. Individuals classified with MetS (NCEP definition), versus those without, showed on average significantly different levels for most inflammatory markers studied. (b) Paired average correlations between 8 metabolic traits and 9 inflammatory markers from the same studies as above, estimated with two methods, and factor analyses on large simulated data, helped in identifying 8 combinations of traits for follow-up
Published: 2014
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22 results on '"Ligthart, S. (Symen)"'

1. Genetic analysis of over half a million people characterises C-reactive protein loci

2. The trans-ancestral genomic architecture of glycemic traits

3. Lifetime risk to progress from pre-diabetes to type 2 diabetes among women and men: comparison between American

4. Molecular Epidemiology of Inflammation: Link with Type 2 Diabetes and Coronary Heart Disease

5. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

6. Association of methylation signals with incident coronary heart disease in an epigenome-wide assessment of circulating tumor necrosis factor α

7. Novel inflammatory markers for incident pre-diabetes and type 2 diabetes: the Rotterdam Study

8. Age at natural menopause and risk of type 2 diabetes

9. Serum magnesium and the risk of prediabetes: a population-based cohort study

10. Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study

11. ADAMTS13 activity as a novel risk factor for incident type 2 diabetes mellitus: a population-based cohort study

12. Obesity and Life Expectancy with and without Diabetes in Adults Aged 55 Years and Older in the Netherlands: A Prospective Cohort Study

13. Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation

14. Tobacco smoking is associated with DNA methylation of diabetes susceptibility genes

15. DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

16. Thyroid function and risk of type 2 diabetes: A population-based prospective cohort study

17. Maternal plasma folate impacts differential DNA methylation in an epigenome-wide meta-analysis of newborns

18. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis

19. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

20. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

21. Vitamin D and C-reactive protein

22. Pleiotropic genes for metabolic syndrome and inflammation

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22 results on '"Ligthart, S. (Symen)"'

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