Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/89811
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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