Maternal perinatal depression and child brain structure at 2-3 years in a South African birth cohort study

• Published in: Translational psychiatry Vol. 13; no. 1; p. 96
• Main Authors: Pellowski, Jennifer A., Wedderburn, Catherine J., Groenewold, Nynke A., Roos, Annerine, Subramoney, Sivenesi, Hoffman, Nadia, Fouche, Jean-Paul, Joshi, Shantanu H., Woods, Roger P., Narr, Katherine L., Zar, Heather J., Donald, Kirsten A., Stein, Dan J.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.03.2023; Nature Publishing Group
• Subjects: 59/57; 631/378; 631/443; 692/699/476/1414; Behavioral Sciences; Biological Psychology; Brain - diagnostic imaging; Brain - pathology; Child; Children & youth; Cohort analysis; Cohort Studies; Depression - complications; Depression - diagnostic imaging; Depression, Postpartum - diagnostic imaging; Female; Humans; Medicine; Medicine & Public Health; Mental depression; Neurosciences; Pharmacotherapy; Pregnancy; Pregnancy Complications; Psychiatry; South Africa; South Africa
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/s41398-023-02395-5

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.