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Parental age as a risk factor for isolated congenital malformations in a Polish population
Anna Materna-Kiryluk1, Katarzyna Wiśniewska, Magdalena Badura-Stronka
1Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, Poland. akiryluk@amp.edu.pl
Insights
Parental age influences congenital malformation risk. Young parents face higher gastroschisis and neural tube defect risks, while advanced parental age is linked to heart defects and certain orofacial clefts.
Area of Science:
- Medical Science
- Genetics
- Epidemiology
Background:
- Inconsistent data exists on parental age and congenital malformations.
- Accurate assessment requires large datasets and adjusted analyses.
Purpose of the Study:
- To investigate the independent associations of maternal and paternal age with isolated non-syndromic congenital malformations.
- To clarify conflicting findings in previous research.
Main Methods:
- Utilized data from the Polish Registry of Congenital Malformations (PRCM).
- Analyzed 8,683 cases of congenital malformations from 902,452 livebirths.
- Employed logistic regression for simultaneous adjustment of maternal and paternal age risks.
Main Results:
- Young maternal and paternal ages independently associated with gastroschisis.
- Young maternal age, not paternal, linked to neural tube defects.
- Advanced maternal and paternal ages independently associated with congenital heart defects.
- Advanced paternal age linked to hypospadias, cleft lip/palate.
- No significant parental age association found for microcephaly, hydrocephaly, intestinal atresia, ano-rectal atresia, renal anomalies, or omphalocele.
Conclusions:
- Parental age is an independent risk factor for specific congenital malformations.
- Maternal and paternal age effects vary depending on the malformation type.
- Findings provide crucial data for risk assessment and counseling.
Abstract:
Currently available data on the relationship between the prevalence of isolated congenital malformations and parental age are inconsistent and frequently divergent. We utilised the data from the Polish Registry of Congenital Malformations (PRCM) to accurately assess the interplay between maternal and paternal age in the risk of isolated non-syndromic congenital malformations. Out of 902 452 livebirths we studied 8683 children aged 0-2 years registered in the PRCM. Logistic regression was used to simultaneously adjust the risk estimates for maternal and paternal age. Our data indicated that paternal and maternal age were independently associated with several congenital malformations. Based on our data, young maternal and paternal ages were independently associated with gastroschisis. In addition, young maternal age, but not young paternal age, carried a higher risk of neural tube defects. Advanced maternal and paternal ages were both independently associated with congenital heart defects. Moreover, there was a positive association between advanced paternal age and hypospadias, cleft palate, and cleft lip (with or without cleft palate). No significant relationships between parental age and the following congenital malformations were detected: microcephaly, hydrocephaly, oesophageal atresia, atresia or stenosis of small and/or large intestine, ano-rectal atresia or stenosis, renal agenesis or hypoplasia, cystic kidney disease, congenital hydronephrosis, diaphragmatic hernia and omphalocele.
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