Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/163915
Título: Potential causal association between gut microbiome and posttraumatic stress disorder
Autor: He, Qiang
Wang, Wenjing
Xu, Dingkang
Xiong, Yang
Tao, Chuanyuan
You, Chao
Ma, Lu
Ma, Junpeng
Nievergelt, Caroline M.
Maihofer, Adam X.
Klengel, Torsten
Liberzon, Israel
Ressler, Kerry J.
Haas, Magali
Koenen, Karestan C.
Ratanatharathorn, Andrew
Stein, Murray B.
Torres, Katy
Aiello, Allison E.
Almli, Lynn M.
Amstadter, Ananda B.
Lugonja, Bozo
Andersen, Søren B.
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.
Luykx, Jurjen J.
Bierut, Laura J.
Bisson, Jonathan I.
Boks, Marco P.
Bolger, Elizabeth A.
Børglum, Anders D.
Bradley, Bekh
Brashear, Megan
Breen, Gerome
Bryant, Richard A.
Bustamante, Angela C.
Lyons, Michael J.
Bybjerg-Grauholm, Jonas
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.
Maples-Keller, Jessica
Domschke, Katharina
Dzubur-Kulenovic, Alma
Erbes, Christopher R.
Evans, Alexandra
Farrer, Lindsay A.
Feeny, Norah C.
Flory, Janine D.
Forbes, David
Franz, Carol E.
Galea, Sandro
Marmar, Charles
Garrett, Melanie E.
Gelaye, Bizu
Gelernter, Joel
Geuze, Elbert
Gillespie, Charles
Uka, Aferdita Goci
Gordon, Scott D.
Guffanti, Guia
Hammamieh, Rasha
Harnal, Supriya
Martin, Alicia R.
Hauser, Michael A.
Heath, Andrew C.
Hemmings, Sian M.J.
Hougaard, David Michael
Jakovljevic, Miro
Jett, Marti
Johnson, Eric Otto
Jones, Ian
Jovanovic, Tanja
Qin, Xue Jun
Martin, Nicholas G.
Junglen, Angela G.
Karstoft, Karen Inge
Kaufman, Milissa L.
Kessler, Ronald
Khan, Alaptagin
Kimbrel, Nathan A.
King, Anthony P.
Koen, Nastassja
Kranzler, Henry R.
Kremen, William S.
Maurer, Douglas
Lawford, Bruce R.
Lebois, Lauren A.M.
Lewis, Catrin E.
Linnstaedt, Sarah D.
Lori, Adriana
Mavissakalian, Matig R.
McFarlane, Alexander
Atkinson, Elizabeth G.
McGlinchey, Regina E.
McLaughlin, Katie A.
McLean, Samuel A.
McLeay, Sarah
Mehta, Divya
Milberg, William P.
Miller, Mark W.
Morey, Rajendra A.
Morris, Charles Phillip
Mors, Ole
Chen, Chia Yen
Mortensen, Preben B.
Neale, Benjamin M.
Nelson, Elliot C.
Nordentoft, Merete
Norman, Sonya B.
O’Donnell, Meaghan
Orcutt, Holly K.
Panizzon, Matthew S.
Peters, Edward S.
Peterson, Alan L.
Choi, Karmel W.
Peverill, Matthew
Pietrzak, Robert H.
Polusny, Melissa A.
Rice, John P.
Ripke, Stephan
Risbrough, Victoria B.
Roberts, Andrea L.
Rothbaum, Alex O.
Rothbaum, Barbara O.
Roy-Byrne, Peter
Coleman, Jonathan R.I.
Ruggiero, Ken
Rung, Ariane
Rutten, Bart P.F.
Saccone, Nancy L.
Sanchez, Sixto E.
Schijven, Dick
Seedat, Soraya
Seligowski, Antonia V.
Seng, Julia S.
Sheerin, Christina M.
Dalvie, Shareefa
Silove, Derrick
Smith, Alicia K.
Smoller, Jordan W.
Solovieff, Nadia
Sponheim, Scott R.
Stein, Dan J.
Sumner, Jennifer A.
Teicher, Martin H.
Thompson, Wesley K.
Trapido, Edward
Duncan, Laramie E.
Uddin, Monica
Ursano, Robert J.
van den Heuvel, Leigh Luella
van Hooff, Miranda
Vermetten, Eric
Vinkers, Christiaan H.
Voisey, Joanne
Wang, Yunpeng
Wang, Zhewu
Werge, Thomas
Logue, Mark W.
Williams, Michelle A.
Williamson, Douglas E.
Winternitz, Sherry
Wolf, Christiane
Wolf, Erika J.
Wolff, Jonathan D.
Yehuda, Rachel
Young, Keith A.
Young, Ross Mc D.
Zhao, Hongyu
Provost, Allison C.
Zoellner, Lori A.
Palavras-chave: Psychiatry and Mental health
Cellular and Molecular Neuroscience
Biological Psychiatry
SDG 3 - Good Health and Well-being
Data: 31-Jan-2024
Resumo: Background: The causal effects of gut microbiome and the development of posttraumatic stress disorder (PTSD) are still unknown. This study aimed to clarify their potential causal association using mendelian randomization (MR). Methods: The summary-level statistics for gut microbiome were retrieved from a genome-wide association study (GWAS) of the MiBioGen consortium. As to PTSD, the Freeze 2 datasets were originated from the Psychiatric Genomics Consortium Posttraumatic Stress Disorder Working Group (PGC-PTSD), and the replicated datasets were obtained from FinnGen consortium. Single nucleotide polymorphisms meeting MR assumptions were selected as instrumental variables. The inverse variance weighting (IVW) method was employed as the main approach, supplemented by sensitivity analyses to evaluate potential pleiotropy and heterogeneity and ensure the robustness of the MR results. We also performed reverse MR analyses to explore PTSD’s causal effects on the relative abundances of specific features of the gut microbiome. Results: In Freeze 2 datasets from PGC-PTSD, eight bacterial traits revealed a potential causal association between gut microbiome and PTSD (IVW, all P < 0.05). In addition, Genus.Dorea and genus.Sellimonas were replicated in FinnGen datasets, in which eight bacterial traits revealed a potential causal association between gut microbiome and the occurrence of PTSD. The heterogeneity and pleiotropy analyses further supported the robustness of the IVW findings, providing additional evidence for their reliability. Conclusion: Our study provides the potential causal impact of gut microbiomes on the development of PTSD, shedding new light on the understanding of the dysfunctional gut-brain axis in this disorder. Our findings present novel evidence and call for investigations to confirm the association between their links, as well as to illuminate the underlying mechanisms.
Descrição: Funding Information: We thank the participants and working staff including the Psychiatric Genomics Consortium Posttraumatic Stress Disorder Working Group, the FinnGen consortium, and the MiBioGen consortium. Publisher Copyright: © 2024, The Author(s).
Peer review: yes
URI: http://hdl.handle.net/10362/163915
DOI: https://doi.org/10.1038/s41398-024-02765-7
ISSN: 2158-3188
Aparece nas colecções:NMS - Artigos em revista internacional com arbitragem científica

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