4.5 Article

Testing lifecourse theories characterising associations between maternal depression and offspring depression in emerging adulthood: the Avon Longitudinal Study of Parents and Children

Journal

Publisher

WILEY
DOI: 10.1111/jcpp.13699

Keywords

accumulation; ALSPAC; depression; depressive symptoms; lifecourse; sensitive periods

Funding

  1. UK Medical Research Council
  2. Wellcome [217065/Z/19/Z]
  3. University of Bristol
  4. Wellcome Trust
  5. UK Economic and Social Research Council [ES/P010229/1, ES/R008930/1]
  6. National Institute of Mental Health of the National Institutes of Health [R01MH113930]

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Maternal depression during different periods, especially in mid-childhood, is associated with increased risk of depressive symptoms in offspring during emerging adulthood, with variations by sex. Accumulation model is more appropriate for males, while exposure to maternal depression in mid-childhood has the largest effect on depressive symptoms in females compared to other time-periods. Early interventions are necessary due to the long-term impact of maternal depression.
Background Maternal depression is a major determinant of offspring mental health. Yet, little is understood about how the duration and timing of maternal depression shapes youth risk for depressive symptoms, which if understood could inform when best to intervene. This study aimed to determine how the timing and duration of maternal depression was related to offspring depression in emerging adulthood, and if these associations varied by sex. Methods We analysed data from the Avon Longitudinal Study of Parents and Children (a prenatal cohort in the Avon area of England, 1991-2003), n = 3,301. We applied the structured lifecourse modelling approach to maternal depression (assessed at 13 points from prenatal period to adolescence) and emerging adult depressive symptoms (age 21). Lifecourse models assessed were accumulation (sum of timepoints when maternal depression was reported), sensitive periods (each period assessed as one during which maternal depression has a stronger effect) and instability (frequent fluctuations in maternal depression). Results Female adolescents (n = 2,132) had higher SMFQ scores (mean = 6.15, SD = 5.90) than males (n = 1,169, mean = 4.87, SD = 4.82). Maternal depression was most common in the infancy period (21.2% males; 21.4% females). For males, accumulation was the most appropriate lifecourse model; for each additional period of maternal depression, depressive symptoms in emerging adulthood increased by 0.11 (95% CI: 0.07, 0.15, one-sided p value <= .001). For females, exposure to maternal depression was associated with increasing depressive symptoms in emerging adulthood, with the largest effect in mid-childhood (increase of 0.27 units, 95% CI 0.03-0.50, p = .015 for difference between mid-childhood and other time-periods) and a smaller, equal effect at all other time-periods (increase of 0.07 units per time-period, 95% CI: 0.03-0.12, p = .002). Conclusions This study highlights the importance of ongoing maternal depression for the development of depression in offspring through to emerging adulthood. Because long-term exposure to maternal depression was particularly important, early interventions are warranted.

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