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Potential causal association between gut microbiome and posttraumatic stress disorder

  • The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Working Group
  • Sichuan University
  • Chinese Academy of Medical Sciences
  • University of California at San Diego
  • Harvard University
  • Broad Institute
  • King's College London
  • University of Cape Town
  • Stanford University
  • National Center for PTSD at Boston VA Healthcare System, Boston, MA, USA
  • Cohen Veterans Bioscience
  • UNC Gillings School of Global Public Health
  • Carter Consulting, Incorporated
  • Virginia Commonwealth University
  • Danish Veteran Centre
  • University of Oslo
  • Minneapolis Veterans Affairs Health Care System
  • Duke University
  • Children's Hospital Boston
  • University Clinical Center Tuzla
  • Department of Nuclear Medicine, University Hospital Mostar, Mostar, Bosnia and Herzegovina
  • Statens Serum Institut
  • Washington University St. Louis
  • Cardiff University
  • University Medical Center Utrecht
  • Aarhus University
  • Atlanta Veterans Administration Health Care System
  • Louisiana State University Health Sciences Center
  • National Institute for Health Research Biomedical Research Centre at University Hospitals Birmingham NHS Foundation Trust and the University of Birmingham, UK
  • University of New South Wales
  • University of Michigan, Ann Arbor
  • Case Western Reserve University
  • Lisbon Institute of Global Mental Health
  • Massachusetts General Hospital
  • University of Würzburg
  • Kent State University
  • University of Freiburg
  • University of Sarajevo
  • Boston University
  • Icahn School of Medicine at Mount Sinai
  • University of Melbourne
  • Department of Veterans Affairs
  • Defense Healthcare Organization, Ministry of Defense, Utrecht, The Netherlands
  • Emory University
  • University Clinical Center of Kosovo
  • Queensland Institute of Medical Research
  • United States Army
  • Stellenbosch University
  • University of Zagreb
  • RTI International
  • University of Pennsylvania
  • Queensland University of Technology
  • University of North Carolina at Chapel Hill
  • University Medical Center of Southern Nevada
  • New York University
  • University of Adelaide
  • Gallipoli Medical Research Foundation
  • The Lundbeck Foundation Initiative for Integrative Psychiatric Research
  • National Center for Posttraumatic Stress Disorder
  • Northern Illinois University
  • University of Texas at San Antonio
  • University of Washington
  • Medical University of South Carolina
  • Maastricht UMC+
  • Universidad Peruana de Ciencias Aplicadas
  • Columbia University
  • Sankt Hans Psychiatric Hospital
  • University of Illinois at Urbana-Champaign
  • Uniformed Services University of the Health Sciences
  • Arq Psychotrauma Expert Group
  • Amsterdam UMC - University of Amsterdam
  • McLean Hospital
  • Baylor Scott & White Health
  • Yale University
  • National Center for PTSD
  • The Danish Veteran Centre
  • Harvard Medical School
  • University Clinical Center of Tuzla
  • University Clinical Center of Mostar
  • Utrecht University
  • Atlanta Veterans Affairs Health Care System
  • University of Oxford
  • Ministry of Defense
  • University Clinical Center of Kosova
  • UMC Utrecht, Netherlands
  • Gallipoli Medical Research Institute
  • Maastricht University
  • Arq Psychotrauma Research Expert Group

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

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.

Original languageEnglish
Article number67
JournalTranslational psychiatry
Volume14
Issue number1
DOIs
Publication statusPublished - 1 Dec 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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