Noruega
Estados Unidos
Noruega
Background and Objectives: Evidence on postpartum antidepressant effectiveness is limited. We sought to deter- mine the association between different timings of antidepressant initiation within the 0–6 months postpartum and mental outcomes at 6- and 18-months following childbirth.
Methods: Using data from the Norwegian Mother, Father and Child Cohort Study (MoBa) linked to a sub-sample of MoBa Genetics, we included 1146 women with psychiatric history before and/or during early pregnancy: 154 (13.4%) antidepressant initiators in the 0–6 months postpartum (37.0% within 0–3, and 63.0% within 4–6 months), and 992 (86.6%) with unmedicated new mental illness episode within same period. Depression/anxiety symptom outcomes at 6 and 18 months postpartum were self-reported. To control for measured confounding, we fit linear and modified Poisson models using overlap weighting, overall and stratified by polygenic score for antidepressant response.
Results: Antidepressant initiators within 0–3 months postpartum had reduced severity of depression/anxiety symptoms at 6, but not at 18 months postpartum, compared with unmedicated women (weighted mean differ- ence (MD): -0.23, 95% CI = -0.39, -0.06) and a 44% lower risk of having active, clinically relevant depressive/ anxiety symptoms at 6 months (weighted RR= 0.56, 95% CI = 0.35, 0.91). No association was observed for initiation at 4–6 months postpartum at the 6-month assessment. The associations were evident only among women having high polygenic score for positive antidepressant response (weighted MD: -0.50, 95% CI: -0.84, -0.16), and that persisted at 18 months.
Conclusions: Initiation of antidepressant in first 3 months postpartum, but not in months 4–6, is associated with reduced severity of depression/anxiety symptoms at 6 months post-delivery. Effects were most evident among women with higher polygenic scores; however, these findings are exploratory and warrant larger studies.