Maternal prenatal co-exposure to air pollution and psychological distress shapes the neonatal gut: microbiota-mediated pathways to early neurodevelopment.
Maternal prenatal co-exposure to air pollution and psychological distress shapes neonatal meconium microbiota composition, with Ruminococcus mediating the relationship between co-exposure patterns and infant neurodevelopment at 3 months of age.
Key Findings
Methods
Three distinct maternal prenatal air pollution-psychological distress co-exposure patterns were identified using a self-organizing map (SOM) among 309 mother-infant pairs.
309 mother-infant pairs were recruited from obstetrics departments of two tertiary hospitals.
The self-organizing map approach was used to identify co-exposure patterns combining air pollution and psychological distress data.
Both general environmental exposures (air pollution) and specific psychological exposures (psychological distress) were measured during pregnancy.
Results
Meconium microbiota composition differed among the three co-exposure patterns at both the phylum and genus levels.
Meconium samples were collected within 48 hours after birth.
Differential features of meconium microbiota in relation to co-exposure patterns were assessed using multivariate association of linear models (MaAsLin).
Differences were observed at both the phylum and genus taxonomic levels across the three co-exposure patterns.
Results
Ruminococcus mediated the relationship between maternal prenatal co-exposure patterns and infant neurodevelopment at 3 months of age.
The indirect effect (IE) of Ruminococcus as a mediator ranged from 0.181 to 0.261.
The mediation effect was statistically significant at pFDR < 0.001.
Infant neurodevelopmental outcomes were assessed using the Ages and Stages Questionnaire-3 (ASQ-3) at 1, 3, and 6 months postpartum.
The mediating role was specifically identified at the 3-month postpartum assessment time point.
Methods
Infant neurodevelopmental outcomes were longitudinally assessed at multiple postpartum time points using a standardized instrument.
The Ages and Stages Questionnaire-3 (ASQ-3) was used to assess neurodevelopmental outcomes.
Assessments were conducted at 1, 3, and 6 months postpartum.
Mediation analysis was used to analyze the role of meconium microbiota in linking co-exposure patterns to neurodevelopmental outcomes.
Conclusions
The study supports inclusion of infant gut microbiota within risk assessment frameworks for maternal prenatal environmental and psychological co-exposures.
The findings provide a scientific basis for identifying intervention targets for high-risk populations.
Air pollution is characterized as a 'general' external exposure and psychological distress as a 'specific' external exposure during pregnancy.
The joint influence of air pollution and psychological distress on early life gut microbiota had not previously been explored prior to this study.
Yang P, Pei Y, Huang Y, Dong M, Cui F, Nie S, et al.. (2026). Maternal prenatal co-exposure to air pollution and psychological distress shapes the neonatal gut: microbiota-mediated pathways to early neurodevelopment.. Gut microbes. https://doi.org/10.1080/19490976.2026.2614451