Association of paternal age with prevalence of selected birth defects

Natalie P Archer1, Peter H Langlois, Lucina Suarez

  • 1Epidemiology and Disease Surveillance Unit, Texas Department of State Health Services, 1100 West 49th Street, Austin, Texas 78756, USA. natalie.archer@dshs.state.tx.us

Insights

Paternal age influences birth defect risks, with younger fathers having higher gastroschisis rates and older fathers having lower trisomy 13 rates. Study data source impacts findings on paternal age and birth defects.

Area of Science:

  • Reproductive Health
  • Pediatrics
  • Genetics

Background:

  • Paternal age's impact on birth defects is understudied compared to maternal age.
  • Texas birth defect registry data (1996-2002) was used to investigate this association.
  • Focus on selected structural birth defects.

Purpose of the Study:

  • To evaluate the association between paternal age and the prevalence of specific structural birth defects.
  • To identify potential risks linked to advanced or young paternal age.

Main Methods:

  • Poisson regression analysis was employed.
  • Prevalence ratios (PRs) and 95% confidence intervals (CIs) were calculated.
  • Adjustments were made for maternal age, race/ethnicity, and parity.

Main Results:

  • Fathers aged 20-24 had increased gastroschisis risk (PR 1.47) compared to fathers 25-29.
  • Fathers aged 40+ had decreased trisomy 13 risk (PR 0.40).
  • No significant association was found for anencephaly or encephalocele; selection bias noted for other defects.

Conclusions:

  • Paternal age is a factor in certain birth defect prevalences.
  • The validity of findings on paternal age and birth defects can be influenced by data source and potential biases.
Abstract

Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Nondisjunction01:21

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers.  Nondisjunction is common during anaphase I or anaphase II of meiosis.  Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...
Probability Laws01:49

Probability Laws

Overview
Pedigree Analysis01:35

Pedigree Analysis

Overview
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Meiosis vs. Mitosis02:57

Meiosis vs. Mitosis

Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...