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Sibling Control Analysis of Perinatal Health and Family Environment Factors Related to Childhood ADHD Symptoms
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Sibling Control Analysis of Perinatal Health and Family Environment Factors Related to Childhood ADHD Symptoms

Michael A. Mooney, Peter Ryabinin, Elizabeth Nousen, Jessica Tipsord, Nathan F. Dieckmann, Sarah L. Karalunas, Megan M. Herting, Molly Nikolas, Joel T. Nigg and Stephen V. Faraone
medRxiv
Cold Spring Harbor Laboratory Press, 1.1
06/17/2025
DOI: 10.1101/2025.06.16.25329516
PMCID: PMC12204260
PMID: 40585166
url
https://doi.org/10.1101/2025.06.16.25329516View
Preprint (Author's original)This preprint has not been evaluated by subject experts through peer review. Preprints may undergo extensive changes and/or become peer-reviewed journal articles. Open Access

Abstract

Background Numerous studies have reported associations between environmental exposures and ADHD. However, whether environmental effects are causal or due to confounding with other familial factors, such as genetic risk, is still unclear. A more complete understanding of which environmental risk factors are causal remains crucial. Methods Using one population (ABCD cohort, N=11646) and one case-control cohort (Oregon ADHD-1000, N=744), we conducted both full-cohort and sibling-control analyses (770 and 152 families in ABCD and Oregon ADHD-1000, respectively) to assess the association of family environment and perinatal risk factors with ADHD symptoms. Within-family effects were compared to effects estimated in the full cohorts. We also assessed the impact of gene-environment correlation using child polygenic risk scores and measures of maternal mental health. Results For both cohorts, full-cohort analyses yielded significant associations between child ADHD symptoms and family conflict, perinatal health factors, and breastfeeding duration (p-values <0.001). These associations were non-significant after accounting for family-level confounds (e.g., genetic risk and shared family environment) in exposure-discordant sibling-control analyses. In the full cohorts, effect sizes were substantially reduced (an average 43.7% decrease in effect size across all exposures tested in the ABCD cohort; average 47.6% decrease in Oregon ADHD-1000) after adjusting for child ADHD polygenic risk and measures related to maternal mental health. Conclusions The full-cohort associations between child ADHD symptoms and environmental risks confirm associations from prior research, but current findings do not indicate direct causal effects. Instead, much or all of the observed risk appears due to confounding with family-level factors, likely including genetic factors. Our results underscore the importance of accounting for familial risk factors that may confound relationships between behavioral traits and environmental exposures by using multiple study designs.
Psychiatry and Clinical Psychology

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