Abstract
Maternal perinatal depression is associated with risk of adverse child developmental outcomes and differences in offspring brain structure. Evidence from low- and middle-income countries is lacking as is an investigation of antenatal, postnatal, and persistent depression in the same sample. In a South African birth cohort, we investigated the effect of antenatal and postpartum maternal depressive symptoms on offspring brain structure at 2–3 years of age. Magnetic resonance imaging was performed, extracting cortical thickness and surface areas in frontal cortex regions of interest and subcortical volumes using FreeSurfer software. Maternal depressive symptoms were measured using the Edinburgh Postpartum Depression Scale and the Beck Depression Inventory II antenatally and at 6–10 weeks, 6 months, 12 months, and 18 months postpartum and analyzed dichotomously and continuously. Linear regressions were used controlling for child age, sex, intracranial volume, maternal education, age, smoking, alcohol use and HIV. 146 children were included with 38 (37%) exposed to depressive symptoms antenatally and 44 (35%) exposed postnatally. Of these, 16 (13%) were exposed to both. Postpartum, but not antenatal, depressive symptoms were associated with smaller amygdala volumes in children (B = −74.73, p = 0.01). Persistent maternal depressive symptoms across pregnancy and postpartum were also independently associated with smaller amygdala volumes (B = −78.61, p = 0.047). Differences in amygdala volumes among children exposed to postnatal as well as persistent maternal depressive symptomatology underscore the importance of identifying women at-risk for depression during the entire perinatal period.
| Original language | English |
|---|---|
| Article number | 96 |
| Journal | Translational Psychiatry |
| Volume | 13 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 2023 |
| Externally published | Yes |
Funding
| Funders | Funder number |
|---|---|
| National Research Foundation of Korea | |
| Medical Research Council | |
| UK Government’s Newton Fund | |
| SA NRF | |
| Carnegie Corporation of New York | |
| National Research Foundation | |
| National Institute on Alcohol Abuse and Alcoholism | R21AA023887, R01 AA026834-01 |
| Wellcome Trust | 203525, 203525/Z/16/Z |
| Bill and Melinda Gates Foundation | OPP 1017641 |
| National Institute of Mental Health | K01MH112443 |
| Academy of Medical Sciences Newton | NAF002/1001 |
| Collaborative Initiative on Fetal Alcohol Spectrum Disorders | U24 AA014811 |
| US Brain and Behavior Foundation | 24467 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 5 Gender Equality
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