Key result
Early-pregnancy SSRI or venlafaxine exposure linked to ~13% higher birth-defect risk, attenuating in sibling analyses.
Why the study?
The association between use of specific SSRIs or venlafaxine in early pregnancy and risk of birth defects, especially cardiovascular defects, accounting for lifestyle and familial confounding, was uncertain.
Cohort
Yes
ObjeCtive To assess whether use of specific selective serotonin reuptake inhibitors (SSRIs) or venlafaxine in early pregnancy is associated with an increased risk of birth defects, with emphasis on cardiovascular birth defects even when accounting for lifestyle or other familial confounding. Multicountry population based cohort study, including sibling a birth defect compared with 3.1% of 2 266 875 unexposed infants, yielding a covariate adjusted odds ratio of 1.13 (95% confidence interval 1.06 to 1.20). In the sibling controlled analysis the adjusted odds ratio decreased to 1.06 (0.91 to 1.24). The odds ratios for any cardiac birth defect with use of any SSRI or venlafaxine were 1.15 (95% confidence interval 1.05 to 1.26) in the covariate adjusted analysis and 0.92 (0.72 to 1.17) in the sibling controlled analysis. For atrial and ventricular septal defects the covariate adjusted odds ratio was 1.17 (1.05 to 1.31). Exposure to any SSRI or venlafaxine increased the prevalence of right ventricular outflow tract obstruction defects, with a covariate adjusted odds ratio of 1.48 (1.15 to 1.89). In the sibling controlled analysis the adjusted odds ratio decreased to 0.56 (0.21 to 1.49) for any exposure to SSRIs or venlafaxine and right ventricular outflow tract obstruction defects.
No takes yet. Share an insight, caveat, or question.
A 2015 study conducted a cohort in Pregnancy. Selective serotonin reuptake inhibitors (SSRIs) or venlafaxine vs. Unexposed was evaluated on Birth defects (OR 1.13, 95% CI 1.06 to 1.20). Exposure to SSRIs or venlafaxine in early pregnancy was associated with an increased risk of birth defects (OR 1.13; 95% CI 1.06-1.20), but the association attenuated in sibling-controlled analysis.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: