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.

Plos One
|March 26, 2015
PubMed

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.

Related Concept Videos

Development of the Heart01:27

Development of the Heart

The development of the human heart, a crucial organ, commences from the mesoderm on the 18th or 19th day after fertilization. This process initiates in the cardiogenic area, a group of mesodermal cells at the embryo's head end, which evolves into elongated strands known as cardiogenic cords. These cords undergo a transformation to form hollow-centered endocardial tubes.
As the embryo undergoes lateral folding, these paired tubes approach each other, merging into a single primitive heart...
3.9K
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.
112.7K
Imbalances in Cardiac Output01:26

Imbalances in Cardiac Output

The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
3.5K
Heart Failure I: Introduction01:27

Heart Failure I: Introduction

Heart failure refers to a clinical syndrome caused by structural or functional cardiac disorders that prevent the heart from pumping an adequate amount of blood to meet the body's metabolic needs. This condition often arises from myocardial infarction or ischemia, leading to decreased cardiac output, reduced tissue perfusion, impaired gas exchange, fluid volume imbalance, and decreased functional ability.Heart failure can result from disruptions in the mechanisms that regulate cardiac output...
1.3K
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...
75.2K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
793