Paternal age and risk for selected birth defects in a large South American sample

Author:

Gili Juan A.123ORCID,Rittler Monica124ORCID,Heisecke Silvina5ORCID,Campaña Hebe126ORCID,Giménez Lucas127ORCID,Santos María Rita1268ORCID,Ratowiecki Julia12ORCID,Cosentino Viviana129ORCID,López Camelo Jorge127ORCID,Poletta Fernando A.127ORCID

Affiliation:

1. Laboratorio de Epidemiología Genética, Centro de Educación Médica e Investigaciones Clínicas‐Consejo Nacional de Investigaciones Científicas y Técnicas (CEMIC‐CONICET) Ciudad Autónoma de Buenos Aires Buenos Aires Argentina

2. Estudio Colaborativo Latinoamericano de Malformaciones Congénitas (ECLAMC), Centro de Educación Médica e Investigaciones Clínicas‐Consejo Nacional de Investigaciones Científicas y Técnicas (CEMIC‐CONICET) Ciudad Autónoma de Buenos Aires Buenos Aires Argentina

3. Instituto Académico Pedagógico de Ciencias Humanas Universidad Nacional de Villa María Córdoba Argentina

4. Hospital Materno Infantil Ramón Sardá Buenos Aires Argentina

5. Dirección de Investigación, Centro de Educación Médica e Investigaciones Clínicas‐Consejo Nacional de Investigaciones Científicas y Técnicas (CEMIC‐ CONICET) Ciudad Autónoma de Buenos Aires Buenos Aires Argentina

6. Comisión de Investigaciones Científicas (CICPBA) Buenos Aires Argentina

7. Instituto Nacional de Genética Médica Populacional (INAGEMP), CEMIC‐CONICET Ciudad Autónoma de Buenos Aires Buenos Aires Argentina

8. Instituto Multidisciplinario de Biología Celular (IMBICE, CONICET‐UNLP‐CICPBA) Buenos Aires Argentina

9. Hospital Interzonal General de Agudos Luisa C. de Gandulfo Buenos Aires Argentina

Abstract

AbstractBackgroundThe relationship between maternal age (MA) and birth defects (BD) has been extensively studied while much less research, mostly with discordant results, has focused on the risk of paternal age (PA) for BD. Furthermore, no consensus has been reached on the best way to control the association of PA with MA.ObjectivesThe aim of the study was to evaluate the risk of PA increase, at 1‐year intervals, for selected BD, especially controlling for the confounding effect of MA.MethodsThe sample comprised of 27,944 liveborns presenting 1 of 18 selected isolated BD. Conditional logistic regressions were applied to evaluate the risk of advanced PA and its yearly increase, adjusting by MA and other variables.ResultsOf the 18 analyzed BD, only the risk for preaxial polydactyly (PreP) showed a significant association with increasing PA, while advanced MA was of low risk. For esophageal and anal atresia, associations with both PA and MA increases were observed.ConclusionsResults support the hypothesis of advanced PA as a risk factor for PreP and helps clarify the so far unexplained nonrandom association between this defect and Down syndrome.

Funder

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

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