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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.
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.
Importance:
Advancing paternal age is associated with increased genetic mutations during spermatogenesis, which research suggests may cause psychiatric morbidity in the offspring. The effects of advancing paternal age at childbearing on offspring morbidity remain unclear, however, because of inconsistent epidemiologic findings and the inability of previous studies to rigorously rule out confounding factors.
Objective:
To examine the associations between advancing paternal age at childbearing and numerous indexes of offspring morbidity.
Design, Setting, And Participants:
We performed a population-based cohort study of all individuals born in Sweden in 1973-2001 (N = 2,615,081), with subsets of the data used to predict childhood or adolescent morbidity. We estimated the risk of psychiatric and academic morbidity associated with advancing paternal age using several quasi-experimental designs, including the comparison of differentially exposed siblings, cousins, and first-born cousins.
Exposure:
Paternal age at childbearing.
Main Outcomes And Measures:
Psychiatric (autism, attention-deficit/hyperactivity disorder, psychosis, bipolar disorder, suicide attempt, and substance use problem) and academic (failing grades and low educational attainment) morbidity.
Results:
In the study population, advancing paternal age was associated with increased risk of some psychiatric disorders (eg, autism, psychosis, and bipolar disorders) but decreased risk of the other indexes of morbidity. In contrast, the sibling-comparison analyses indicated that advancing paternal age had a dose-response relationship with every index of morbidity, with the magnitude of the associations being as large or larger than the estimates in the entire population. Compared with offspring born to fathers 20 to 24 years old, offspring of fathers 45 years and older were at heightened risk of autism (hazard ratio [HR] = 3.45; 95% CI, 1.62-7.33), attention-deficit/hyperactivity disorder (HR = 13.13; 95% CI, 6.85-25.16), psychosis (HR = 2.07; 95% CI, 1.35-3.20), bipolar disorder (HR = 24.70; 95% CI, 12.12-50.31), suicide attempts (HR = 2.72; 95% CI, 2.08-3.56), substance use problems (HR = 2.44; 95% CI, 1.98-2.99), failing a grade (odds ratio [OR] = 1.59; 95% CI, 1.37-1.85), and low educational attainment (OR = 1.70; 95% CI, 1.50-1.93) in within-sibling comparisons. Additional analyses using several quasi-experimental designs obtained commensurate results, further strengthening the internal and external validity of the findings.
Conclusions And Relevance:
Advancing paternal age is associated with increased risk of psychiatric and academic morbidity, with the magnitude of the risks being as large or larger than previous estimates. These findings are consistent with the hypothesis that new genetic mutations that occur during spermatogenesis are causally related to offspring morbidity.
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