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Objective A robust literature has identified associations between prenatal maternal depression and adverse child social-emotional and cognitive outcomes. The majority of prior research is from high-income countries despite increased reporting of perinatal depression in low/middle-income countries (LMICs). Additionally, despite the comorbidity between depression and anxiety, few prior studies have examined their joint impact on child neurodevelopment. The objective of the current analysis was to examine associations between prenatal maternal depression and anxiety with child social-emotional and cognitive development in a cohort from the Western Cape Province of South Africa. Design Prenatal maternal depression and anxiety were measured using the Edinburgh Postnatal Depression Scale and the State-Trait Anxiety Inventory Scale at 20-24 weeks’ gestation. Child neurobehaviour was assessed at age 3 using the Brief Infant-Toddler Social Emotional Assessment and the Bayley Scales of Infant Development III Screening Test (BSID-III ST). We used linear regression models to examine the independent and joint association between prenatal maternal depression, anxiety and child developmental outcomes. Results Participants consisted of 600 maternal-infant dyads (274 females; gestational age at birth: 38.89 weeks±2.03). Children born to mothers with both prenatal depression and trait anxiety had higher social-emotional problems (mean difference: 4.66; 95% CI 3.43 to 5.90) compared with children born to mothers with no prenatal depression or trait anxiety, each condition alone, or compared with mothers with depression and state anxiety. Additionally, children born to mothers with prenatal maternal depression and trait anxiety had the greatest reduction in mean cognitive scores on the BSID-III ST (mean difference: -1.04; 95% CI -1.99 to -0.08). Conclusions The observed association between comorbid prenatal maternal depression and chronic anxiety with subsequent child social-emotional and cognitive development underscores the need for targeting mental health support among perinatal women in LMICs to improve long-term child neurobehavioural outcomes.
Participants were a subset of infants with available outcome data at age 3 enrolled in the Safe Passage study conducted by the Prenatal Alcohol and SIDS and Stillbirth Network, a multi-centre study investigating the role of prenatal exposure in risk for sudden infant death syndrome, stillbirth and fetal alcohol spectrum disorders. Eligibility criteria for the Safe Passage study included the ability to provide informed consent in English or Afrikaans, 16 years of age or older at the time of consent, and a gestational age between 6 weeks and 40 weeks at the time of consent based on estimated delivery date.31 Exclusion criteria for prenatal maternal enrolment into the Safe Passage study included planned therapeutic abortion, moving out of the catchment area prior to estimated date of delivery and clinical judgement. Maternal-infant medical charts were abstracted to obtain maternal age at delivery, gestational age at birth, mode of delivery and the infant’s biological sex. Measures to collect prenatal alcohol, tobacco and recreational drug exposure have been previously described.31 32 Prenatal maternal alcohol and tobacco use behaviours were previously characterised using cluster analysis.33 34 Through study specific case report forms, participants indicated demographic and socioeconomic information including race, maternal educational attainment, household crowding (persons per room in household), access to running water inside the house, prenatal care during pregnancy and marital status. Information regarding maternal mental health during pregnancy was obtained at 20–24 weeks’ gestation. Depressive symptoms were measured using the Edinburgh Postnatal Depression Scale (EPDS), a depression screening tool developed to specifically assess depressive symptoms in perinatal women where higher scores indicate more severe depressive symptoms.35 36 The EPDS is widely used and has been validated in English and Afrikaans in South Africa.35 37 Prior studies have used a cut-off score of ≥12 or ≥13 to be indicative of major depression within perinatal women living in South Africa.35 37 Maternal anxiety symptoms were measured using the State-Trait Anxiety Inventory (STAI),38 an anxiety screening tool to distinguish anxiety symptoms from depressive symptoms which has also been validated in both languages.39 The STAI has two subscales, state anxiety which reflects the participant’s current state of anxiety when completing the questionnaires and trait anxiety, which is thought to be consistent across time and reflect personality traits. In HICs, the STAI has a cut-off score of ≥40 on both the state anxiety and trait anxiety subscales to indicate a threshold for clinical levels of anxiety. Based on these prior studies, we used a cut-off of ≥13 to indicate maternal depression, a cut-off of >40 on the STAI-state subscale to indicate state anxiety and a cut-off of >40 on the STAI-trait subscale to indicate trait anxiety. The Bayley Scales of Infant Development III Screening Test (BSID-III ST) were designed as a rapid assessment of cognitive, language and motor functioning in infants and young children in order to determine if a child’s development is within normal limits and identify risk for developmental delay. The BSID-III ST has high test–retest reliability: cognitive (0.85), receptive language (0.88), expressive language (0.88), fine motor (0.82) and gross motor (0.86). Although the BSID-III ST does not identify degree of impairment, the cut-off points indicate whether a child shows competence in age-appropriate tasks, evidence of emerging age-appropriate skills and evidence of being at risk for developmental delay. The BSID has been validated and widely used throughout South Africa.40 41 The Brief Infant-Toddler Social and Emotional Assessment (BITSEA) is a 42-item parental report measure of social-emotional development, behavioural problems and delays in competence.42 Domains assessed within the BITSEA include: externalising (activity/impulsivity, aggression/defiance, peer aggression), internalising (depression/withdrawal, anxiety, separation distress, inhibition to novelty), dysregulation (sleep, negative emotionality, eating, sensory sensitivity) and competence (compliance, attention, imitation/play, mastery motivation, empathy and pro-social peer relations).42 Findings from the BITSEA validation study provide preliminary support for the BITSEA as a reliable and valid brief screener for infant-toddler social-emotional and behavioural problems in addition to delays in competence.43 When used in socioeconomically and ethnically diverse community-based populations, the BITSEA demonstrated excellent test–retest reliability and good inter-rater agreement between parents.42 Using multiple linear regression models, we estimated independent and joint effects of maternal depression and state and trait anxiety on social-emotional problem, social emotional competence and cognitive development scores. Two, separate four-level categorical prenatal maternal mental health variables were created to assess the impact of prenatal maternal depression, trait anxiety and state anxiety. We created a prenatal maternal depression and trait anxiety variable with four categories: (1) no prenatal depression or trait anxiety (n=199; 33.17%, reference category), (2) prenatal depression only (106; 17.67%), (3) prenatal trait anxiety only (n=68; 11.33%) and (4) prenatal maternal depression and trait anxiety (n=227; 37.83%) (table 1). In separate models we additionally examined the independent and joint effects of prenatal maternal depression and state anxiety. We created a prenatal maternal depression and state anxiety variable with four categories: (1) no prenatal depression or state anxiety (n=248; 41.33%; reference category), (2) prenatal depression only (n=237; 39.50%), (3) prenatal state anxiety only (n=19; 3.17%) and (4) prenatal maternal depression and state anxiety (n=96; 16%) (table 1). For each regression model, either no prenatal maternal depression or trait anxiety or no prenatal maternal depression and state anxiety was set as the reference category. Minimally adjusted models included sex, gestational age at birth and age at follow-up as covariates. Fully adjusted models additionally controlled for prenatal maternal alcohol use, prenatal maternal tobacco use, maternal employment status at delivery, maternal educational attainment at delivery, parity and the household crowding index. We used missing indicator methods and median imputation to account for missing categorical and continuous covariate data, respectively (described in table 1). All analyses were performed in SAS software V.9.4 (SAS Institute). Sociodemographic characteristics