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Research work
Potential causal association between gut microbiome and posttraumatic stress disorder
Authors
Allison E. Aiello
Lynn M. Almli
+184 more
Ananda B. Amstadter
Søren B. Andersen
Ole A. Andreassen
Paul A. Arbisi
Allison E. Ashley-Koch
Elizabeth G. Atkinson
S. Bryn Austin
Esmina Avdibegovic
Dragan Babić
Dewleen G. Baker
Jean C. Beckham
Laura J. Bierut
Jonathan I. Bisson
Marco P. Boks
Elizabeth A. Bolger
Bekh Bradley
Megan Brashear
Gerome Breen
Richard A. Bryant
Angela C. Bustamante
Jonas Bybjerg-Grauholm
Marie Bækvad-Hansen
Anders D. Børglum
Joseph R. Calabrese
José M. Caldas-de-Almeida
Chia Yen Chen
Karmel W. Choi
Jonathan R.I. Coleman
Anders M. Dale
Shareefa Dalvie
Mark J. Daly
Nikolaos P. Daskalakis
Jürgen Deckert
Douglas L. Delahanty
Michelle F. Dennis
Seth G. Disner
Katharina Domschke
Laramie E. Duncan
Alma Dzubur-Kulenovic
Christopher R. Erbes
Alexandra Evans
Lindsay A. Farrer
Norah C. Feeny
Janine D. Flory
David Forbes
Carol E. Franz
Sandro Galea
Melanie E. Garrett
Bizu Gelaye
Joel Gelernter
Elbert Geuze
Charles Gillespie
Scott D. Gordon
Guia Guffanti
Magali Haas
Rasha Hammamieh
Supriya Harnal
Michael A. Hauser
Qiang He
Andrew C. Heath
Sian M.J. Hemmings
David Michael Hougaard
Miro Jakovljevic
Marti Jett
Eric Otto Johnson
Ian Jones
Tanja Jovanovic
Angela G. Junglen
Karen Inge Karstoft
Milissa L. Kaufman
Ronald C. Kessler
Alaptagin Khan
Nathan A. Kimbrel
Anthony P. King
Torsten Klengel
Nastassja Koen
Karestan C. Koenen
Henry R. Kranzler
William S. Kremen
Bruce R. Lawford
Lauren A.M. Lebois
Catrin E. Lewis
Israel Liberzon
Sarah D. Linnstaedt
Mark W. Logue
Adriana Lori
Bozo Lugonja
Jurjen J. Luykx
Michael J. Lyons
Junpeng Ma
Lu Ma
Adam X. Maihofer
Jessica Maples-Keller
Charles Marmar
Alicia R. Martin
Nicholas G. Martin
Douglas Maurer
Matig R. Mavissakalian
Alexander McFarlane
Regina E. McGlinchey
Katie A. McLaughlin
Samuel A. McLean
Sarah McLeay
Divya Mehta
William P. Milberg
Mark W. Miller
Rajendra A. Morey
Charles Phillip Morris
Ole Mors
Preben B. Mortensen
Benjamin M. Neale
Elliot C. Nelson
Caroline M. Nievergelt
Merete Nordentoft
Sonya B. Norman
Holly K. Orcutt
and other
Meaghan O’Donnell
Matthew S. Panizzon
Edward S. Peters
Alan L. Peterson
Matthew Peverill
Robert H. Pietrzak
Melissa A. Polusny
Allison C. Provost
Xue Jun Qin
Andrew Ratanatharathorn
Kerry J. Ressler
John P. Rice
Stephan Ripke
Victoria B. Risbrough
Andrea L. Roberts
Alex O. Rothbaum
Barbara O. Rothbaum
Peter Roy-Byrne
Ken Ruggiero
Ariane Rung
Bart P.F. Rutten
Nancy L. Saccone
Sixto E. Sanchez
Dick Schijven
Soraya Seedat
Antonia V. Seligowski
Julia S. Seng
Christina M. Sheerin
Derrick Silove
Alicia K. Smith
Jordan W. Smoller
Nadia Solovieff
Scott R. Sponheim
Dan J. Stein
Murray B. Stein
Jennifer A. Sumner
Chuanyuan Tao
Martin H. Teicher
Wesley K. Thompson
Katy Torres
Edward Trapido
Monica Uddin
Aferdita Goci Uka
Robert J. Ursano
Leigh Luella van den Heuvel
Miranda van Hooff
Eric Vermetten
Christiaan H. Vinkers
Joanne Voisey
Wenjing Wang
Yunpeng Wang
Zhewu Wang
Thomas Werge
Michelle A. Williams
Douglas E. Williamson
Sherry Winternitz
Christiane Wolf
Erika J. Wolf
Jonathan D. Wolff
Yang Xiong
Dingkang Xu
Rachel Yehuda
Chao You
Keith A. Young
Ross Mc D. Young
Hongyu Zhao
Lori A. Zoellner
Publication date
1 January 2024
Publisher
Doi
Abstract
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).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.publishersversionpublishe
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Hochschulbibliothekszentrum des Landes Nordrhein-Westfalen (hbz)
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