Browsing by Author "Winkler, T. W."

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    Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions.
    (School of Hygiene and Public Health of Johns Hopkins University,Baltimore., 2019) de Vries, P. S.; Brown, M. R.; Bentley, A. R.; Sung, Y. J.; Winkler, T. W.; Ntalla, I.; Schwander, K.; Kraja, A. T.; Guo, X.; Franceschini, N.; Cheng, C. Y.; Sim, X.; Vojinovic, D.; Huffman, J. E.; Musani, S. K.; Li, C.; Feitosa, M.F.; Richard, M.A.; Noordam, R.; Aschard, H.; Bartz, T. M.; Bielak, L. F.; Deng, X.; Dorajoo, R.; Lohman, K.K.; Manning, A. K.; Rankinen, T.; Smith, A. V.; Tajuddin, S. M.; Evangelou, E.; Graff, M.; Alver, M.; Boissel, M.; Chai, J. F.; Chen, X.; Divers, J.; Gandin, I.; Gao, C.; Goel, A.; Hagemeijer, Y.; Harris, S. E.; Hartwig, F. P.; He, M.; Horimoto, A. R. V. R.; Hsu, F. C.; Jackson, A. U.; Kasturiratne, A.; Komulainen, P.; Kühnel, B.; Laguzzi, F.; Lee, J. H.; Luan, J.; Lyytikäinen, L. P.; Matoba, N.; Nolte, I. M.; Pietzner, M.; Riaz, M.; Said, M. A.; Scott, R. A.; Sofer, T.; Stancáková, A.; Takeuchi, F.; Tayo, B. O.; van der Most, P. J.; Varga, T. V.; Wang, Y.; Ware, E. B.; Wen, W.; Yanek, L. R.; Zhang, W.; Zhao, J. H.; Afaq, S.; Amin, N.; Amini, M.; Arking, D. E.; Aung, T.; Ballantyne, C.; Boerwinkle, E.; Broeckel, U.; Campbell, A.; Canouil, M.; Charumathi, S.; Chen, Y. I.; Connell, J. M.; de Faire, U.; de Las Fuentes, L.; de Mutsert, R.; de Silva, H.J.; Ding, J.; Dominiczak, A. F.; Duan, Q.; Eaton, C. B.; Eppinga, R.N.; Faul, J. D.; Fisher, V.; Forrester, T.; Franco, O. H.; Friedlander, Y.; Ghanbari, M.; Giulianini, F.; Grabe, H. J.; Grove, M. L.; Gu, C. C.; Harris, T. B.; Heikkinen, S.; Heng, C. K.; Hirata, M.; Hixson, J. E.; Howard, B. V.; Ikram, M. A.; InterAct Consortium; Jr. Jacobs, D. R.; Johnson, C.; Jonas, J. B.; Kammerer, C. M.; Katsuya, T.; Khor, C. C.; Kilpeläinen, T. O.; Koh, W. P.; Koistinen, H. A.; Kolcic, I.; Kooperberg, C.; Krieger, J. E.; Kritchevsky, S. B.; Kubo, M.; Kuusisto, J.; Lakka, T. A.; Langefeld, C. D.; Langenberg, C.; Launer, L. J.; Lehne, B.; Lemaitre, R. N.; Li, Y.; Liang, J.; Liu, J.; Liu, K.; Loh, M.; Louie, T.; Mägi, R.; Manichaikul, A. W.; McKenzie, C. A.; Meitinger, T.; Metspalu, A.; Milaneschi, Y.; Milani, L.; Mohlke, K. L.; Jr. Mosley, T. H.; Nelson, C. P.; Mukamal, K. J.; Nalls, M. A.; Nauck, M.; Sotoodehnia, N.; O'Connell, J. R.; Palmer, N. D.; Pazoki, R.; Pedersen, N. L.; Peters, A.; Peyser, P. A.; Polasek, O.; Poulter, N.; Raffel, L. J.; Raitakari, O. T.; Reiner, A. P.; Rice, T. K.; Rich, S. S.; Robino, A.; Robinson, J. G.; Rose, L. M.; Rudan, I.; Schmidt, C. O.; Schreiner, P. J.; Scott, W. R.; Sever, P.; Shi, Y.; Sidney, S.; Sims, M.; Smith, B. H.; Smith, J. A.; Snieder, H.; Starr, J. M.; Strauch, K.; Tan, N.; Taylor, K. D.; Teo, Y. Y.; Tham, Y. C.; Uitterlinden, A. G.; van Heemst, D.; Vuckovic, D.; Waldenberger, M.; Wang, L.; Wang, Y.; Wang, Z.; Wei, W. B.; Williams, C.; Sr Wilson, G.; Wojczynski, M. K.; Yao, J.; Yu, B.; Yu, C.; Yuan, J. M.; Zhao, W.; Zonderman, A. B.; Becker, D. M.; Boehnke, M.; Bowden, D. W.; Chambers, J. C.; Deary, I. J.; Esko, T.; Farrall, M.; Franks, P. W.; Freedman, B. I.; Froguel, P.; Gasparini, P.; Gieger, C.; Horta, B. L.; Kamatani, Y.; Kato, N.; Kooner, J. S.; Laakso, M.; Leander, K.; Lehtimäki, T.; Lifelines Cohort, Groningen,; The Netherlands (Lifelines Cohort Study); Magnusson, P. K. E.; Penninx, B.; Pereira, A. C.; Rauramaa, R.; Samani, N.J.; Scott, J.; Shu, X. O.; van der Harst, P.; Wagenknecht, L. E.; Wang, Y. X.; Wareham, N. J.; Watkins, H.; Weir, D. R.; Wickremasinghe, A.R.; Zheng, W.; Elliott, P.; North, K. E.; Bouchard, C.; Evans, M. K.; Gudnason, V.; Liu, C. T.; Liu, Y.; Psaty, B. M.; Ridker, P. M.; van Dam, R. M.; Kardia, S. L. R.; Zhu, X.; Rotimi, C. N.; Mook-Kanamori, D. O.; Fornage, M.; Kelly, T. N.; Fox, E. R.; Hayward, C.; van Duijn, C. M.; Tai, E. S.; Wong, T. Y.; Liu, J.; Rotter, J. I.; Gauderman, W. J.; Province, M. A.; Munroe, P. B.; Rice, K.; Chasman, D. I.; Cupples, L. A.; Rao, D. C.; Morrison, A. C.
    An individual's lipid profile is influenced by genetic variants and alcohol consumption, but the contribution of interactions between these exposures has not been studied. We therefore incorporated gene-alcohol interactions into a multi-ancestry genome-wide association study of levels of high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and triglycerides. We included 45 studies in Stage 1 (genome-wide discovery) and 66 studies in Stage 2 (focused follow-up), for a total of 394,584 individuals from five ancestry groups. Genetic main and interaction effects were jointly assessed by a 2 degrees of freedom (DF) test, and a 1 DF test was used to assess the interaction effects alone. Variants at 495 loci were at least suggestively associated (P < 1 × 10-6) with lipid levels in Stage 1 and were evaluated in Stage 2, followed by combined analyses of Stage 1 and Stage 2. In the combined analysis of Stage 1 and Stage 2, 147 independent loci were associated with lipid levels at P < 5 × 10-8 using 2 DF tests, of which 18 were novel. No genome-wide significant associations were found testing the interaction effect alone. The novel loci included several genes (PCSK5, VEGFB, and A1CF) with a putative role in lipid metabolism based on existing evidence from cellular and experimental models.
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    Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
    (Nature Publications, 2019) Kilpeläinen, T.O.; Bentley, A.R.; Noordam, R.; Sung, Y. J.; Schwander, K.; Winkler, T. W.; Jakupović, H.; Chasman, D. I.; Manning, A.; Ntalla, I.; Aschard, H.; Brown, M. R.; de Las Fuentes, L.; Franceschini, N.; Guo, X.; Vojinovic, D.; Aslibekyan, S.; Feitosa, M. F.; Kho, M.; Musani, S. K.; Richard, M.; Wang, H.; Wang, Z.; Bartz, T. M.; Bielak, L. F.; Campbell, A.; Dorajoo, R.; Fisher, V.; Hartwig, F. P.; Horimoto, A. R. V. R.; Li, C.; Lohman, K. K.; Marten, J.; Sim, X.; Smith, A. V.; Tajuddin, S. M.; Alver, M.; Amini, M.; Boissel, M.; Chai, J. F.; Chen, X.; Divers, J.; Evangelou, E.; Gao, C.; Graff, M.; Harris, S. E.; He, M.; Hsu, F. C.; Jackson, A. U.; Zhao, J. H.; Kraja, A. T.; Kühnel, B.; Laguzzi, F.; Lyytikäinen, L. P.; Nolte, I. M.; Rauramaa, R.; Riaz, M.; Robino, A.; Rueedi, R.; Stringham, H. M.; Takeuchi, F.; van der Most, P. J.; Varga, T. V.; Verweij, N.; Ware, E. B.; Wen, W.; Li, X.; Yanek, L. R.; Amin, N.; Arnett, D. K.; Boerwinkle, E.; Brumat, M.; Cade, B.; Canouil, M.; Chen, Y. I.; Concas, M. P.; Connell, J.; de Mutsert, R.; de Silva, H.J.; de Vries, P.S.; Demirkan, A.; Ding, J.; Eaton, C. B.; Faul, J. D.; Friedlander, Y.; Gabriel, K. P.; Ghanbari, M.; Giulianini, F.; Gu, C. C.; Gu, D.; Harris, T. B.; He J, J.; Heikkinen, S.; Heng, C. K.; Hunt, S. C.; Ikram, M. A.; Jonas, J. B.; Koh, W. P.; Komulainen, P.; Krieger, J. E.; Kritchevsky, S. B.; Kutalik, Z.; Kuusisto, J.; Langefeld, C. D.; Langenberg, C.; Launer, L. J.; Leander, K.; Lemaitre, R. N.; Lewis, C. E.; Liang, J.; Lifelines Cohort Study; Liu, J.; Mägi, R.; Manichaikul, A.; Meitinger, T.; Metspalu, A.; Milaneschi, Y.; Mohlke, K. L.; Mosley, T. H.; Murray, A. D.; Nalls, M. A.; Nang, E. K.; Nelson, C. P.; Nona, S.; Norris, J. M.; Nwuba, C. V.; O'Connell, J.; Palmer, N. D.; Papanicolau, G. J.; Pazoki, R.; Pedersen, N. L.; Peters, A.; Peyser, P. A.; Polasek, O.; Porteous, D. J.; Poveda, A.; Raitakari, O. T.; Rich, S. S.; Risch, N.; Robinson, J. G.; Rose, L. M.; Rudan, I.; Schreiner, P. J.; Scott, R. A.; Sidney, S. S.; Sims, M.; Smith, J. A.; Snieder, H.; Sofer, T.; Starr, J. M.; Sternfeld, B.; Strauch, K.; Tang, H.; Taylor, K. D.; Tsai, M. Y.; Tuomilehto, J.; Uitterlinden, A. G.; van der Ende, M. Y.; van Heemst, D.; Voortman, T.; Waldenberger, M.; Wennberg, P.; Wilson, G.; Xiang, Y. B.; Yao, J.; Yu, C.; Yuan, J. M.; Zhao, W.; Zonderman, A. B.; Becker, D. M.; Boehnke, M.; Bowden, D. W.; de Faire, U.; Deary, I. J.; Elliott, P.; Esko, T.; Freedman, B. I.; Froguel, P.; Gasparini, P.; Gieger, C.; Kato, N.; Laakso, M.; Lakka, T. A.; Lehtimäki, T.; Magnusson, P. K. E.; Oldehinkel, A. J.; Penninx, B. W. J. H.; Samani, N. J.; Shu, X. O.; van der Harst, P.; Van Vliet-Ostaptchouk, J. V.; Vollenweider, P.; Wagenknecht, L. E.; Wang, Y. X.; Wareham, N. J.; Weir, D. R.; Wu, T.; Zheng, W.; Zhu, X.; Evans, M. K.; Franks, P. W.; Gudnason, V.; Hayward, C.; Horta, B. L.; Kelly, T. N.; Liu, Y.; North, K. E.; Pereira, A. C.; Ridker, P. M.; Tai, E. S.; van Dam, R. M.; Fox, E. R.; Kardia, S. L. R.; Liu, C. T.; Province, M. A.; Mook-Kanamori, D. O.; Redline, S.; van Duijn, C. M.; Rotter, J. I.; Kooperberg, C. B.; Gauderman, W. J.; Psaty, B. M.; Rice, K.; Munroe, P. B.; Fornage, M.; Cupples, L. A.; Rotimi, C. N.; Morrison, A. C.; Rao, D. C.; Loos, R. J. F.
    Many genetic loci affect circulating lipid levels, but it remains unknown whether lifestyle factors, such as physical activity, modify these genetic effects. To identify lipid loci interacting with physical activity, we performed genome-wide analyses of circulating HDL cholesterol, LDL cholesterol, and triglyceride levels in up to 120,979 individuals of European, African, Asian, Hispanic, and Brazilian ancestry, with follow-up of suggestive associations in an additional 131,012 individuals. We find four loci, in/near CLASP1, LHX1, SNTA1, and CNTNAP2, that are associated with circulating lipid levels through interaction with physical activity; higher levels of physical activity enhance the HDL cholesterol-increasing effects of the CLASP1, LHX1, and SNTA1 loci and attenuate the LDL cholesterol-increasing effect of the CNTNAP2 locus. The CLASP1, LHX1, and SNTA1 regions harbor genes linked to muscle function and lipid metabolism. Our results elucidate the role of physical activity interactions in the genetic contribution to blood lipid levels.