Aug 2026· Gut microbes· Vol 18· 0 citations· 68 references
Medicine
TL;DR
This study provides the first data-driven evidence for a potential causal role of gut microbiota in the pathophysiology of depression in humans, and employs state-of-the-art causal inference tools within Judea Pearl's framework.
Abstract
Abstract Major Depressive Disorder (MDD) is a highly prevalent, severe mental health condition that constitutes one of the leading causes of disability worldwide. While recent animal studies suggest a causal role of the gut microbiome in the pathophysiology of MDD models, evidence in humans is still unclear due to small sample sizes, inconsistent clinical assessment of MDD diagnosis, and methodological limitations regarding causal inference in cross-sectional data. Here, we explicitly address these shortcomings to investigate the potential causal link between the gut microbiome and MDD: First, we replicate previously reported microbiome-depression associations using one of the largest multicenter MDD cohorts for which microbiome data and in-depth diagnostic assessment are available (N = 1,269 MDD patients and controls). We find a significant difference between healthy controls and MDD patients for the relative abundance of four taxa: Eggerthella, Hungatella, Coprobacillus, and Lachnospiraceae FCS020. Second, we employ state-of-the-art, fully data-driven causal inference tools within Judea Pearl's framework, allowing us to derive model constraints from the data rather than relying on potentially strong, unrealistic assumptions. Using this approach, we found evidence for Eggerthella and Hungatella as potential causal contributors to MDD. Furthermore, we show that the potential causal effects of Eggerthella and Hungatella on MDD persist beyond the influence of body mass index, revealing two distinct potential causal pathways linking the gut microbiome to MDD. Finally, the difference in relative abundance of these taxa between healthy and MDD patients was independent of antidepressant medication. Our study provides the first data-driven evidence for a potential causal role of gut microbiota in the pathophysiology of depression in humans.
Gut microbiome provides a candidate approach for potential risk stratification in psychiatric populations, and MDD + RBD may represent a biologically distinct depression subtype associated with potential neurodegenerative risk.
Yuhua Yang, Ningning Li, Li Zhou et al.· Molecular Psychiatry· 0 citations
The results highlight the potential of gut bacterial and viral biomarkers as candidate biomarkers and potential auxiliary tools for MDD assessment and suggest that integrating multi-domain microbial features may improve prediction accuracy.
Xuan Wang, Wei Chen, Hanlin Zhang et al.· Frontiers in Cellular and In...· 0 citations
Evidence emerged that gut microbiome variations seem to be associated with brain structural and functional alterations in both Major Depressive Disorder and Bipolar Depression, with preliminary evidence also suggesting significant neurobiological effects of probiotics in MDD.
Federico Bottaro, P. Enrico, C. Cabasino et al.· Journal of Affective Disorde...· 0 citations
The microbiota-gut-brain axis has emerged as a key framework for understanding how peripheral biological systems influence brain function and behaviour, and microbial metabolites and immune mediators emerge as key mediators, although direct causal mechanisms in humans remain incompletely established.
Sultan Almarzooqi, Lidya K. Yassin, Fatima Alnuaimi et al.· Translational Psychiatry· 0 citations
The results suggested that associations between proinflammatory gut microbiota and the herpes simplex virus type 1 infection pathway may contribute to the onset of MDD through inflammatory processes.
Gut microbiota-targeted interventions are effective for alleviating depressive symptoms in adults with MDD-a finding supported by low-to-moderate certainty of evidence, but this finding should be interpreted with caution due to the limited certainty of evidence.
Shuo Jin, Chenming Li, Ni Sun et al.· Nutrition reviews· 0 citations
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