Potential causal association between gut microbiome and posttraumatic stress disorder.
| dc.contributor.author | He, Qiang | |
| dc.contributor.author | Wang, Wenjing | |
| dc.contributor.author | Xu, Dingkang | |
| dc.contributor.author | Xiong, Yang | |
| dc.contributor.author | Tao, Chuanyuan | |
| dc.contributor.author | You, Chao | |
| dc.contributor.author | Ma, Lu | |
| dc.contributor.author | Ma, Junpeng | |
| dc.date.accessioned | 2024-05-01T18:20:10Z | |
| dc.date.available | 2024-05-01T18:20:10Z | |
| dc.date.issued | 2024-01 | |
| dc.description.abstract | BackgroundThe 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).MethodsThe 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.ResultsIn 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.ConclusionOur 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. | |
| dc.identifier | 10.1038/s41398-024-02765-7 | |
| dc.identifier.issn | 2158-3188 | |
| dc.identifier.issn | 2158-3188 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Springer Science and Business Media LLC | |
| dc.relation.ispartof | Translational psychiatry | |
| dc.relation.isversionof | 10.1038/s41398-024-02765-7 | |
| dc.rights.uri | ||
| dc.subject | Psychiatric Genomics Consortium Posttraumatic Stress Disorder Working Group | |
| dc.subject | Humans | |
| dc.subject | Reproducibility of Results | |
| dc.subject | Stress Disorders, Post-Traumatic | |
| dc.subject | Dietary Supplements | |
| dc.subject | Genome-Wide Association Study | |
| dc.subject | Gastrointestinal Microbiome | |
| dc.title | Potential causal association between gut microbiome and posttraumatic stress disorder. | |
| dc.type | Journal article | |
| pubs.begin-page | 67 | |
| pubs.issue | 1 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | Sanford School of Public Policy | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Biostatistics & Bioinformatics | |
| pubs.organisational-group | Molecular Genetics and Microbiology | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Psychiatry & Behavioral Sciences | |
| pubs.organisational-group | Medicine, Nephrology | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | University Institutes and Centers | |
| pubs.organisational-group | Duke Institute for Brain Sciences | |
| pubs.organisational-group | Duke Molecular Physiology Institute | |
| pubs.organisational-group | Center for Child and Family Policy | |
| pubs.organisational-group | Psychiatry & Behavioral Sciences, Behavioral Medicine & Neurosciences | |
| pubs.publication-status | Published | |
| pubs.volume | 14 |
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