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Maternal oxidative stress during pregnancy associated with emotional and behavioural problems in early childhood: implications for foetal programming.

Authors :
Pham C
Thomson S
Chin ST
Vuillermin P
O'Hely M
Burgner D
Tanner S
Saffery R
Mansell T
Bong S
Holmes E
Sly PD
Gray N
Ponsonby AL
Source :
Molecular psychiatry [Mol Psychiatry] 2023 Sep; Vol. 28 (9), pp. 3760-3768. Date of Electronic Publication: 2023 Oct 16.
Publication Year :
2023

Abstract

Childhood mental disorders, including emotional and behavioural problems (EBP) are increasingly prevalent. Higher maternal oxidative stress (OS) during pregnancy ( <subscript>mat</subscript> OS <subscript>preg</subscript> ) is linked to offspring mental disorders. Environmental factors contribute to <subscript>mat</subscript> OS <subscript>preg</subscript> . However, the role of <subscript>mat</subscript> OS <subscript>preg</subscript> in childhood EBP is unclear. We investigated the associations between (i) <subscript>mat</subscript> OS <subscript>preg</subscript> and offspring EBP; (ii) social and prenatal environmental factors and <subscript>mat</subscript> OS <subscript>preg</subscript> ; and (iii) social and prenatal factors and childhood EBP and evaluated whether <subscript>mat</subscript> OS <subscript>preg</subscript> mediated these associations. Maternal urinary OS biomarkers, 8-hydroxyguanosine (8-OHGua; an oxidative RNA damage marker) and 8-hydroxy-2'-deoxyguanosine (8-OHdG; an oxidative DNA damage marker), at 36 weeks of pregnancy were quantified by liquid chromatography-mass spectrometry in a population-derived birth cohort, Barwon Infant Study (n = 1074 mother-infant pairs). Social and prenatal environmental factors were collected by mother-reported questionnaires. Offspring total EBP was measured by Child Behavior Checklist Total Problems T-scores at age two (n = 675) and Strengths and Difficulties Questionnaire Total Difficulties score at age four (n = 791). Prospective associations were examined by multivariable regression analyses adjusted for covariates. Mediation effects were evaluated using counterfactual-based mediation analysis. Higher maternal urinary 8-OHGua at 36 weeks ( <subscript>mat</subscript> 8-OHGua <subscript>36w</subscript> ) was associated with greater offspring total EBP at age four (β = 0.38, 95% CI (0.07, 0.69), P = 0.02) and age two (β = 0.62, 95% CI (-0.06, 1.30), P = 0.07). Weaker evidence of association was detected for 8-OHdG. Five early-life factors were associated with both <subscript>mat</subscript> 8-OHGua <subscript>36w</subscript> and childhood EBP (P-range < 0.001-0.05), including lower maternal education, socioeconomic disadvantage and prenatal tobacco smoking. These risk factor-childhood EBP associations were partly mediated by higher <subscript>mat</subscript> 8-OHGua <subscript>36w</subscript> (P-range = 0.01-0.05). Higher <subscript>mat</subscript> OS <subscript>preg</subscript> , particularly oxidant RNA damage, is associated with later offspring EBP. Effects of some social and prenatal lifestyle factors on childhood EBP were partly mediated by <subscript>mat</subscript> OS <subscript>preg</subscript> . Future studies are warranted to further elucidate the role of early-life oxidant damage in childhood EBP.<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
1476-5578
Volume :
28
Issue :
9
Database :
MEDLINE
Journal :
Molecular psychiatry
Publication Type :
Academic Journal
Accession number :
37845496
Full Text :
https://doi.org/10.1038/s41380-023-02284-9