This observational cohort study used Danish national registers to identify all children born from 1998-2015 and their relatives through 3-generation family linkage, comprising full maternal cousin pairs. The study examined associations between maternal diagnoses previously linked to offspring autism (e.g., postpartum hemorrhage, personality disorders, epilepsy) and autism diagnosis in cousins.
Comparisons were made between parallel and cross cousins to infer mechanisms. Several maternal diagnoses, including postpartum hemorrhage, personality disorders, and epilepsy, were associated with autism in both parallel and cross cousins, consistent with shared direct genetic effects. Other conditions, such as false labor, recurrent major depressive disorder, other anxiety disorders, and systemic connective tissue involvement, showed stronger associations in parallel than cross cousins, supporting additional indirect genetic effects operating through the prenatal environment.
Hazard ratios were estimated separately in parallel and cross cousins, but specific values, absolute numbers, p-values, and confidence intervals were not reported. Safety data, including adverse events and discontinuations, were not reported. The study is observational and uses hazard ratios to estimate associations; it infers mechanisms but does not establish causation.
Key limitations include the lack of reported effect sizes, confidence intervals, and p-values, as well as the absence of follow-up duration and sample size. Findings are based on registry data and family linkage, which may introduce unmeasured confounding. Practice relevance was not reported, and clinicians should not overstate the strength of effects without reported effect sizes or confidence intervals.
View Original Abstract ↓
Despite autism's prominent genetic etiology and early-life origins, parsing genetic effects contributing to the condition into those that operate directly (via allelic transmission to offspring) vs. indirectly (via influencing prenatal environment) remains challenging. We examined this using a novel design leveraging 3-generation family linkage in Danish national registers. The cohort included all children born in Denmark from 1998-2015 and their relatives identified through 3-generation family linkage. The analytic sample comprised full maternal cousin pairs, including parallel (children of mother's sister) and cross cousins (children of mother's brother). Exposures were diagnoses in the index mother previously associated with offspring autism; the outcome was autism diagnosis in cousins of the index child. We used Cox proportional hazards models to estimate associations separately in parallel and cross cousins, followed by comparisons of these hazard ratios to infer mechanisms. Several maternal diagnoses (e.g., postpartum hemorrhage, personality disorders, epilepsy) were associated with autism in both parallel and cross cousins, consistent with shared direct genetic effects. Other conditions (e.g., false labor, recurrent major depressive disorder, other anxiety disorders, systemic connective tissue involvement) showed stronger associations in parallel than cross cousins, supporting additional indirect genetic effects operating through the prenatal environment. Adjustment for the same diagnosis in the cousin's own mother did not substantially change estimates, providing no evidence for an additional role of non-genetic mechanisms associated with the diagnosis. These findings suggest that both direct and indirect genetic effects contribute to observed links between maternal health and offspring autism, highlighting etiologic heterogeneity and highlighting a registry-based family design to separate these pathways without genetic data.