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Analysis of Congenital Heart Defects in Mouse Embryos Using Qualitative and Quantitative Histological Methods
Published on: March 10, 2020
Paternal age and offspring congenital heart defects: a national cohort study
Xiu Juan Su1, Wei Yuan2, Guo Ying Huang3
1Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China; Section for Epidemiology, Department of Public health, Aarhus University, Aarhus, Denmark.
Insights
Advanced paternal age is linked to a higher risk of patent ductus arteriosus (PDA) in offspring. This study found no overall link between paternal age and congenital heart defects (CHDs).
Area of Science:
- Reproductive Health
- Pediatric Cardiology
- Epidemiology
Background:
- Paternal age is a potential risk factor for congenital heart defects (CHDs) due to accumulated germ cell mutations.
- Previous evidence on the paternal age-CHD link is inconclusive, and subtype-specific risks are unknown.
Purpose of the Study:
- To investigate the association between paternal age and the risk of offspring CHDs and their common subtypes.
- To analyze data from a large Danish national cohort to clarify this relationship.
Main Methods:
- Utilized Danish national register data for 1,893,899 singletons born between 1977 and 2008.
- Employed Cox proportional hazards models to estimate hazard ratios for paternal age and CHD subtypes (PDA, VSD, ASD, TOF, CoA).
- Controlled for maternal age in subanalyses.
Main Results:
- No overall association was found between paternal age and congenital heart defects (CHDs).
- Paternal age over 45 was associated with a 69% increased risk of patent ductus arteriosus (PDA) compared to fathers aged 25-29.
- This association remained significant after adjusting for maternal age.
Conclusions:
- Advanced paternal age is specifically associated with an increased risk of patent ductus arteriosus (PDA) in offspring.
- The study highlights a subtype-specific effect of paternal age on congenital heart defects.
- Findings suggest a targeted approach for monitoring PDA risk in relation to paternal age.
Abstract:
Paternal age has been associated with offspring congenital heart defects (CHDs), which might be caused by increased mutations in the germ cell line because of cumulated cell replications. Empirical evidences, however, remain inconclusive. Furthermore, it is unknown whether all subtypes of CHDs are affected by paternal age. We aimed to explore the relationship between paternal age and the risk of offspring CHDs and its five common subtypes using national register data in Denmark. A total of 1,893,899 singletons born in Denmark from 1977 to 2008 were included in this national-based cohort study. Cox's proportion hazards model with robust sandwich estimate option was used to estimate the hazards ratio (95% confidence interval) for the associations between paternal age and all CHDs, as well as subtypes of CHDs (patent ductus arteriosus (PDA), ventricular septal defect (VSD), atrial septal defect (ASD), tetralogy of fallot (TOF) and coarctation of the aorta (CoA)). We did not observe an overall association between paternal age and offspring CHDs. However, compared to the paternal age of 25-29 years, paternal age of older than 45 years was associated with a 69% increased risk of PDA (HR45+ = 1.69, 95%CI:1.17-2.43). We observed similar results when subanalyses were restricted to children born to mothers of 27-30 years old. After taking into consideration of maternal age, our data suggested that advanced paternal age was associated with an increased prevalence of one subtype of offspring congenital heart defects (CHDs), namely patent ductus arteriosus (PDA).
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