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Study 9 of 13ARA 290 literatureGut microbes · Observational2026

Antenatal depressive symptoms impair offspring neurodevelopment by inducing maternal gut microbiota dysbiosis during pregnancy.

Maternal antenatal depressive symptoms may negatively impact infant neurodevelopment through changes in gut microbiota, highlighting the importance of maternal mental health during pregnancy.

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Where it sits

this study against the rest of the ara 290 corpus
2
Preclinical
9
Observational · this one
0
Open-label
0
Randomised
2
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Summary and findings

This study measured the association between maternal antenatal depressive symptoms and offspring neurodevelopment in a cohort of 2053 pregnant women. It reported that elevated depressive symptoms were significantly associated with delayed infant neurodevelopment. Additionally, fecal microbiota transplantation (FMT) from women with depressive symptoms led to impaired cognitive outcomes in offspring.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Not reported in abstract.2026

Abstract

The authors’ words, as Gut microbes supplied them

The effects of maternal antenatal depression (AND) across different stages of pregnancy on offspring neurodevelopment remain poorly understood, and the underlying microbiota-related mechanisms are largely unknown. In a multicenter prospective cohort of 2053 pregnant women, we found that elevated depressive symptoms at any trimester were significantly associated with delayed infant neurodevelopment. Using a nested case‒control design with 16S rRNA sequencing of 504 maternal fecal samples, we identified a consistent reduction of butyrate-producing bacteria and disruption of amino acid metabolism in women with AND symptoms - features that correlated with poorer infant cognitive outcomes. To establish causality, fecal microbiota transplantation (FMT) from women with AND symptoms was administered to germ-free dams, resulting in impaired intestinal barrier integrity, heightened neuroinflammatory signaling, and altered polyunsaturated fatty acid and amino acid metabolism in fetal brains at E18.5, leading to postnatal cognitive deficits in the offspring. Remarkably, maternal butyrate supplementation partially rescued these molecular and neurodevelopmental abnormalities. Together, these findings reveal a mechanistic link between maternal mood, gut microbial ecology, and fetal brain development, and identify the maternal gut microbiota and its metabolites as potential therapeutic targets to prevent the intergenerational effects of antenatal depression.

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