Paternal age at childbearing and offspring psychiatric and academic morbidity

Brian M D'Onofrio1, Martin E Rickert1, Emma Frans2

  • 1Department of Psychological and Brain Sciences, Indiana University, Bloomington.

JAMA Psychiatry
|March 1, 2014
PubMed

Insights

Older fathers increase offspring risks for autism, ADHD, psychosis, and academic issues. Advancing paternal age is linked to higher rates of psychiatric and academic morbidity in children.

Area of Science:

  • Reproductive biology
  • Genetics
  • Psychiatry
  • Epidemiology

Background:

  • Advancing paternal age is linked to increased genetic mutations during spermatogenesis.
  • Previous research suggests a potential link between paternal age and offspring psychiatric morbidity.
  • Epidemiologic findings are inconsistent, and confounding factors limit previous studies.

Purpose of the Study:

  • To investigate the association between advancing paternal age at childbearing and offspring morbidity.
  • To examine risks for psychiatric and academic morbidity in relation to paternal age.

Main Methods:

  • Population-based cohort study of 2,615,081 individuals born in Sweden (1973-2001).
  • Utilized quasi-experimental designs, including sibling, cousin, and first-born cousin comparisons.
  • Assessed psychiatric (autism, ADHD, psychosis, bipolar disorder, suicide attempt, substance use) and academic (failing grades, low educational attainment) morbidity.

Main Results:

  • Advancing paternal age showed a dose-response relationship with all assessed psychiatric and academic morbidities in sibling-comparison analyses.
  • Offspring of fathers aged 45+ had significantly higher risks for autism, ADHD, psychosis, bipolar disorder, suicide attempts, substance use problems, failing grades, and low educational attainment compared to offspring of fathers aged 20-24.
  • Quasi-experimental designs yielded consistent results, strengthening the findings' validity.

Conclusions:

  • Advancing paternal age is associated with a substantially increased risk of psychiatric and academic morbidity in offspring.
  • The magnitude of these risks is comparable to or greater than previous estimates.
  • Findings support the hypothesis that de novo genetic mutations during spermatogenesis contribute causally to offspring morbidity.
Abstract

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