Specific parental depression symptoms as risk markers for new-onset depression in high-risk offspring
Becky Mars1, Gordon T Harold, Kit K Elam
1Institute of Psychological Medicine and Clinical Neurosciences, Medical Research Council (MRC) Centre for Neuropsychiatric Genetics and Genomics, Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff.
Insights
Parental appetite or weight changes, specifically loss, are significant risk factors for offspring depression. This highlights the importance of examining specific depression symptoms in families with recurrent depression history.
Area of Science:
- Psychiatry
- Genetics
- Developmental Psychology
Background:
- Recurrent parental depression poses a risk to offspring mental health.
- Understanding specific parental depression symptoms as risk markers is crucial for early intervention.
Purpose of the Study:
- To determine if specific parental depression symptoms predict future depression in high-risk offspring.
- To investigate the hypothesis that parental symptoms impacting offspring are of greatest importance.
Main Methods:
- Longitudinal family study with 337 parent-child dyads.
- Parents had a history of recurrent unipolar depression; offspring aged 9-17.
- New-onset mood disorder in offspring assessed via Child and Adolescent Psychiatric Assessment.
Main Results:
- Parental loss of appetite or weight strongly predicted offspring mood disorder (OR=4.47) and depression symptoms (β=0.12).
- This association remained significant after controlling for parental depression severity and other confounds.
Conclusions:
- Parental appetite/weight loss is a clinical risk marker for offspring depression.
- Highlights the need to study depression heterogeneity for better risk prediction.
- Further research is needed to explore underlying biological and environmental mechanisms.
Objective:
To disaggregate the depression construct and investigate whether specific depression symptoms in parents with a history of recurrent depression are clinical risk markers for future depression in their high-risk offspring. Our hypothesis was that parental symptoms of the type that might impact offspring would most likely be of greatest importance.
Method:
Data were drawn from a longitudinal high-risk family study. Families were mainly recruited from primary care and included 337 parent-child dyads. Parents had a history of recurrent DSM-IV unipolar depression and were aged 26-55 years. Their offspring (197 female and 140 male) were aged 9-17 years. Three assessments were conducted between April 2007 and April 2011. Ninety-one percent of families (n = 305) provided full interview data at baseline and at least 1 follow-up, of which 291 were included in the primary analysis. The main outcome measure was new-onset DSM-IV mood disorder in the offspring, which was assessed using the Child and Adolescent Psychiatric Assessment.
Results:
Of the 9 DSM-IV depression symptoms, parental change in appetite or weight, specifically loss of appetite or weight, most strongly predicted new-onset mood disorder (odds ratio [OR] = 4.47; 95% CI, 2.04-9.79; P < .001) and future depression symptoms in the offspring (β = 0.12; B = 0.21; 95% CI, 0.00-0.42; P = .050). The cross-generational association was not accounted for by measures of parental depression severity (total depression symptom score, episode recurrence, age at onset, and past impairment or hospitalization) or other potential confounds (parent physical health, eating disorder, or medication).
Conclusions:
Findings from this study suggest that loss of appetite or weight in parents with a history of recurrent depression is a marker of risk for depression in their offspring. The findings highlight the importance of examining depression heterogeneity. The biological and environmental mechanisms underlying this finding require investigation.
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