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Association of Antidepressant Use During Pregnancy With Risk of Neurodevelopmental Disorders in Children
Elizabeth A Suarez1, Brian T Bateman2, Sonia Hernández-Díaz3
1Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Insights
Antidepressant use during pregnancy did not increase the risk of neurodevelopmental disorders in children. However, exposure may indicate a need for early screening and intervention for pregnant individuals and their offspring.
Area of Science:
- Perinatal Psychiatry
- Child Neurodevelopment
- Pharmacoepidemiology
Background:
- Previous studies suggest a link between prenatal antidepressant exposure and child neurodevelopmental disorders.
- Confounding factors such as parental mental health, genetics, and environment may explain these associations.
- The critical period of synaptogenesis (gestational week 19 to delivery) is a key focus for exposure assessment.
Purpose of the Study:
- To investigate the association between maternal antidepressant use during pregnancy and neurodevelopmental outcomes in children.
- To differentiate the direct effects of antidepressants from confounding factors in large healthcare datasets.
Main Methods:
- A large-scale cohort study utilizing health care utilization data from Medicaid Analytic eXtract (MAX) and IBM MarketScan Research Database.
- Inclusion of approximately 1.93 million pregnancies in MAX and 1.25 million in MarketScan, with children followed up to 14 years.
- Advanced statistical methods, including propensity score fine stratification, discontinuers comparison, and sibling analyses, were employed to control for confounding.
Main Results:
- Crude analyses suggested a potential doubling of risk for neurodevelopmental outcomes with prenatal antidepressant exposure.
- However, fully adjusted analyses, particularly sibling analyses, revealed no statistically significant association between antidepressant use and neurodevelopmental disorders.
- Hazard ratios for specific disorders, including autism spectrum disorder and ADHD, were consistently close to 1.0 across adjusted models.
Conclusions:
- Antidepressant use during pregnancy is not causally linked to an increased risk of neurodevelopmental disorders in children.
- The observed crude associations likely stem from unmeasured confounding factors.
- Prenatal antidepressant exposure may serve as a marker for identifying individuals who could benefit from early screening and targeted interventions.
Importance:
Antidepressant use during pregnancy has been associated with neurodevelopmental disorders in children in some studies. However, results may be explained by uncontrolled confounding by parental mental health status, genetics, and environmental factors.
Objective:
To evaluate the association between antidepressant use in pregnancy and neurodevelopmental outcomes in children.
Design, Setting, And Participants:
This cohort study of health care utilization data was separated into cohorts of publicly and privately insured pregnant individuals and their children nested in the Medicaid Analytic eXtract (MAX; 2000-2014) and the IBM MarketScan Research Database (MarketScan; 2003-2015). A total of 1.93 million pregnancies in MAX and 1.25 million pregnancies in MarketScan were recorded. Children were followed from birth until outcome diagnosis, disenrollment, death, or end of study (maximum 14 years). Analyses were conducted between August 2020 and July 2021.
Exposures:
Dispensing of antidepressant medication from gestational week 19 until delivery, the period of synaptogenesis.
Main Outcomes And Measures:
Neurodevelopmental disorders in children defined using validated algorithms. Early pregnancy exposure was considered in sensitivity analyses, and approaches to confounding adjustment included propensity score fine stratification, discontinuers comparison, and sibling analyses.
Results:
Among the individuals included in the analysis, there were 145 702 antidepressant-exposed and 3 032 745 unexposed pregnancies; the mean (SD) age among the antidepressant exposed and unexposed was 26.2 (5.7) and 24.3 (5.8) years in MAX and 32.7 (4.6) and 31.9 (4.6) years in MarketScan, respectively; and in MAX, which collected information on race and ethnicity, 72.4% of the antidepressant-exposed and 37.1% of the unexposed individuals were White. Crude results suggested up to a doubling in risk of neurodevelopmental outcomes associated with antidepressant exposure; however, no association was observed in the most fully adjusted analyses. When comparing antidepressant-exposed and unexposed siblings, hazard ratios were 0.97 (95% CI, 0.88-1.06) for any neurodevelopmental disorder, 0.86 (95% CI, 0.60-1.23) for autism spectrum disorder, 0.94 (95% CI, 0.81-1.08) for attention-deficit/hyperactivity disorder, 0.77 (95% CI, 0.42-1.39) for specific learning disorders, 1.01 (95% CI, 0.88-1.16) for developmental speech/language disorder, 0.79 (95% CI, 0.54-1.17) for developmental coordination disorder, 1.00 (95% CI, 0.45-2.22) for intellectual disability, and 0.95 (95% CI, 0.80-1.12) for behavioral disorders. Results were generally consistent for antidepressant classes and drugs and across exposure windows.
Conclusions And Relevance:
The results of this cohort study suggest that antidepressant use in pregnancy itself does not increase the risk of neurodevelopmental disorders in children. However, given strong crude associations, antidepressant exposure in pregnancy may be an important marker for the need of early screening and intervention.
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