Background Prenatal stress predicts offspring anxiety and depressive disorders and placental microRNA (miRNA) signaling in a sex-specific manner. Methods We prospectively examined associations of miRNAs measured in placental tissue and in extracellular vesicles (EVs) from prenatal maternal blood with preschool Child Behavior Checklist (CBCL) outcomes [Total Problems, Internalizing Problems, Diagnostic and Statistical Manual of Mental Disorders-oriented scales for Anxiety and Affective Problems]. We first used Least Absolute Shrinkage and Selection Operator regressions embedded in a stability selection procedure to identify miRNAs most consistently associated with CBCL outcomes. Then multivariable linear regressions examined all selected miRNAs in relation to each outcome within a single model. Finally, we examined miRNA-CBCL associations stratified by lifetime maternal stress measured prenatally and fetal sex and fit models including a three-way interaction term for stress, sex, and miRNA expression. Results Among miRNAs selected by the machine learning models, miR-330-5p in blood EVs and miR-548aw in placenta emerged as top candidates related to CBCL outcomes. When jointly considering fetal sex and lifetime maternal stress as modifiers, the association between blood miR-330-5p and affective problems was positive in females exposed to low stress (β: 0.73, 95%CI: 0.15, 1.3) but negative in males with high stress exposure (β: -1.64, 95%CI: -3.01, -0.28), pint=0.03. Placental Let-7b expression was negatively associated with total problems among males with high stress exposure (β: -6.58, 95%CI: -12.45, -0.71) but positively associated among males with low stress (β: 3.63, 95%CI: 1.26, 6.01), pint=0.04. Top KEGG pathways included Hippo, FoxO, and PI3K/mTOR signaling. Conclusions Prenatal miRNA signaling may play a role in sex-specific lifetime maternal stress effects on neuropsychological development.
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Wright et al. (2026) studied this question.
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