Evidence map›Paper›PMID 42825823›Full record

ArticleEuropean journal of pediatrics2026

Parental and grandparental age in relation to Down syndrome risk and congenital heart disease in affected children: a case-control study in Peru.

Hugo Abarca-Barriga, Alejandra Paola Espinosa Suárez, Miara Yahaira Amayo Cabrera

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Article in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Hugo Abarca-BarrigaCarrera Profesional de Medicina Humana, Universidad Científica del Sur, Lima, Perú. habarca@cientifica.edu.pe.
Alejandra Paola Espinosa SuárezCarrera Profesional de Medicina Humana, Universidad Científica del Sur, Lima, Perú.
Miara Yahaira Amayo CabreraCarrera Profesional de Medicina Humana, Universidad Científica del Sur, Lima, Perú.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to assess the association between grandparental age and the risk of Down syndrome and evaluate the relationship between paternal age and congenital heart disease (CHD) among affected children in Peru. A retrospective case-control study was conducted at a national pediatric referral center in Peru, including 290 participants (145 cases with free trisomy 21 and 145 controls without genetic disorders). Logistic regression models were used to estimate the odds ratios (ORs) and 95% confidence intervals (CIs). Parental ages were higher in cases than in controls, but there were no significant differences in grandparental ages. Maternal age was the strongest risk factor for Down syndrome (OR = 1.16 per additional year; 95% CI: 1.09-1.23). No significant association was found between maternal grandmother's age and Down syndrome (OR = 0.96 per additional year; 95% CI: 0.91-1.02). Paternal age ≥ 32.6 years (categorical analysis based on the Liu-derived cut-off) was associated with an increased risk of congenital heart disease in the presence of FT21, compared with a reference group combining FT21 without CHD and healthy controls (aOR = 3.64; 95% CI: 1.96-6.77).

conclusionIn this Latin American cohort, maternal age remains the primary risk factor for Down syndrome, with no evidence supporting an effect of maternal grandmother's age at the birth of the mother. Notably, advanced paternal age was independently associated with higher odds of congenital heart disease among children with Down syndrome. These findings warrant confirmation in independent populations before being considered for clinical application. WHAT IS KNOWN: • Advanced maternal age is the main established risk factor for Down syndrome. • The maternal grandmother's age at the birth of the mother remains uncertain, with inconsistent evidence. The contribution of paternal age to congenital heart disease in affected individuals has been insufficiently studied. WHAT IS NEW: • In this case-control study from a Latin American population, the maternal grandmother's age at the birth of the mother was not associated with DS • Advanced paternal age was independently associated with higher odds of congenital heart disease among children with Down syndrome.

Indexed as

Down SyndromeGrandparentsHeart Defects, CongenitalMaternal AgePaternal AgeAdolescentAdultCase-Control StudiesChildChild, PreschoolFemaleHumansInfantLogistic ModelsMaleOdds RatioCongenital heart diseaseDown syndromeGrandparentsPaternal age

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.