Título: | International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci |
Autor: | Nievergelt, Caroline M. Maihofer, Adam X. Klengel, Torsten Atkinson, Elizabeth G. Chen, Chia Yen Choi, Karmel W. Coleman, Jonathan R.I. Dalvie, Shareefa Duncan, Laramie E. Gelernter, Joel Levey, Daniel F. Andreassen, Ole A. Arbisi, Paul A. Ashley-Koch, Allison E. Austin, S. Bryn Avdibegovic, Esmina Babić, Dragan Bækvad-Hansen, Marie Baker, Dewleen G. Beckham, Jean C. Bierut, Laura J. Martin, Nicholas G. Bisson, Jonathan I. Boks, Marco P. Bolger, Elizabeth A. Børglum, Anders D. Bradley, Bekh Brashear, Megan Breen, Gerome Bryant, Richard A. Bustamante, Angela C. Bybjerg-Grauholm, Jonas Maurer, Douglas Calabrese, Joseph R. JM, Caldas-de-Almeida Dale, Anders M. Daly, Mark J. Daskalakis, Nikolaos P. Deckert, Jürgen Delahanty, Douglas L. Dennis, Michelle F. Disner, Seth G. Domschke, Katharina Mavissakalian, Matig R. Dzubur-Kulenovic, Alma Erbes, Christopher R. Evans, Alexandra Farrer, Lindsay A. Feeny, Norah C. Flory, Janine D. Forbes, David Franz, Carol E. Galea, Sandro Garrett, Melanie E. McFarlane, Alexander Gelaye, Bizu Geuze, Elbert Gillespie, Charles Uka, Aferdita Goci Gordon, Scott D. Guffanti, Guia Hammamieh, Rasha Harnal, Supriya Hauser, Michael A. Heath, Andrew C. McGlinchey, Regina E. Hemmings, Sian M.J. Hougaard, David Michael Jakovljevic, Miro Jett, Marti Johnson, Eric Otto Jones, Ian Jovanovic, Tanja Qin, Xue Jun Junglen, Angela G. Karstoft, Karen Inge McLaughlin, Katie A. Kaufman, Milissa L. Kessler, Ronald Khan, Alaptagin Kimbrel, Nathan A. King, Anthony P. Koen, Nastassja Kranzler, Henry R. Kremen, William S. Lawford, Bruce R. Lebois, Lauren A.M. McLean, Samuel A. Lewis, Catrin E. Linnstaedt, Sarah D. Lori, Adriana Lugonja, Bozo Luykx, Jurjen J. Lyons, Michael J. Maples-Keller, Jessica Marmar, Charles Martin, Alicia R. McLeay, Sarah Mehta, Divya Milberg, William P. Logue, Mark W. Miller, Mark W. Morey, Rajendra A. Morris, Charles Phillip Mors, Ole Mortensen, Preben B. Neale, Benjamin M. Nelson, Elliot C. Nordentoft, Merete Norman, Sonya B. O'Donnell, Meaghan Polimanti, Renato Orcutt, Holly K. Panizzon, Matthew S. Peters, Edward S. Peterson, Alan L. Peverill, Matthew Pietrzak, Robert H. Polusny, Melissa A. Rice, John P. Ripke, Stephan Risbrough, Victoria B. Provost, Allison C. Roberts, Andrea L. Rothbaum, Alex O. Rothbaum, Barbara O. Roy-Byrne, Peter Ruggiero, Ken Rung, Ariane Rutten, Bart P.F. Saccone, Nancy L. Sanchez, Sixto E. Schijven, Dick Ratanatharathorn, Andrew Seedat, Soraya Seligowski, Antonia V. Seng, Julia S. Sheerin, Christina M. Silove, Derrick Smith, Alicia K. Smoller, Jordan W. Sponheim, Scott R. Stein, Dan J. Stevens, Jennifer S. Stein, Murray B. Sumner, Jennifer A. Teicher, Martin H. Thompson, Wesley K. Trapido, Edward Uddin, Monica Ursano, Robert J. van den Heuvel, Leigh Luella Van Hooff, Miranda Vermetten, Eric Vinkers, Christiaan H. Torres, Katy Voisey, Joanne Wang, Yunpeng Wang, Zhewu Werge, Thomas Williams, Michelle A. Williamson, Douglas E. Winternitz, Sherry Wolf, Christiane Wolf, Erika J. Wolff, Jonathan D. Aiello, Allison E. Yehuda, Rachel Young, Ross Mc D. Young, Keith A. Zhao, Hongyu Zoellner, Lori A. Liberzon, Israel Ressler, Kerry J. Haas, Magali Koenen, Karestan C. Almli, Lynn M. Amstadter, Ananda B. Andersen, Søren B. |
Palavras-chave: | Chemistry(all) Biochemistry, Genetics and Molecular Biology(all) Physics and Astronomy(all) |
Data: | 8-Out-2019 |
Resumo: | The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5-20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson's disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and expanding GWAS beyond European ancestry populations. |
Descrição: | This work was funded by Cohen Veterans Bioscience, the NIMH/U.S. Army Medical Research and Materiel Command Grant R01MH106595 to C.M.N., I.L., K.J.R. and K.C.K., One Mind, and supported by 5U01MH109539 to the Psychiatric Genomics Consortium. Statistical Analysis were carried out on the NL Genetic Cluster computer (URL) hosted by SURFsara. Genotyping of samples was supported in part through the Stanley Center for Psychiatric Genetics at the Broad Institute of MIT and Harvard. This research has been conducted using the UK biobank resource under application number 16577. This work would not have been possible without the contributions of the investigators who comprise the PGC-PTSD working group, and especially the more than 206,000 research participants worldwide who shared their life experiences and biological samples with PGC-PTSD investigators. Full acknowledgements are in the Supplementary Note 2. |
Peer review: | yes |
URI: | http://www.scopus.com/inward/record.url?scp=85073062147&partnerID=8YFLogxK http://hdl.handle.net/10362/89811 |
DOI: | https://doi.org/10.1038/s41467-019-12576-w |
ISSN: | 2041-1723 |
Aparece nas colecções: | NMS: CEDOC - Artigos em revista internacional com arbitragem científica
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