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Descriptive epidemiology of non-syndromic complete atrioventricular canal defects
A J Agopian1, Mousumi Moulik, Monesha Gupta-Malhotra
1Center for Human Genetics, Division of Epidemiology, Human Genetics and Environmental Sciences, University of Texas School of Public Health, Houston, TX 77030 USA.
Insights
Maternal diabetes and obesity are linked to an increased risk of non-syndromic complete atrioventricular canal defects (CAVC) in infants. This study highlights these conditions as significant risk factors for this common heart defect.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Public Health
Background:
- Complete atrioventricular canal defects (CAVC) are prevalent congenital heart conditions.
- Epidemiologic data on non-syndromic CAVC and its risk factors remain limited.
- Understanding risk factors is crucial for prevention and early intervention strategies.
Purpose of the Study:
- To investigate the association between parental sociodemographic and reproductive factors and the risk of non-syndromic CAVC in offspring.
- Specifically, to examine the roles of maternal diabetes and obesity as potential risk factors.
Main Methods:
- Utilized data from the Texas Birth Defects Registry, a population-based registry.
- Conducted Poisson regression analyses on 563 cases of non-syndromic CAVC.
- Evaluated sociodemographic and reproductive parental factors, including diabetes and obesity.
Main Results:
- Maternal pregestational diabetes showed a significant association (aPR 6.74; 95% CI 3.67, 12.37).
- Gestational diabetes was also associated with increased risk (aPR 1.69; 95% CI 1.03, 2.79).
- Maternal obesity demonstrated a significant association (aPR 1.69; 95% CI 1.24, 2.30).
Conclusions:
- Non-syndromic CAVC is identified as a birth defect associated with maternal diabetes.
- Maternal obesity is also linked to an increased risk of non-syndromic CAVC.
- These findings contribute to the understanding of risk factors for congenital heart defects.
Background:
Complete atrioventricular canal defects (CAVC) are a common heart defect, but few epidemiologic studies have evaluated non-syndromic CAVC. Risk factors for non-syndromic CAVC have not been well established.
Methods:
To assess the relationship between risk for non-syndromic CAVC in offspring and several sociodemographic and reproductive parental factors, including maternal diabetes and obesity, we conducted Poisson regression analyses, using data ascertained through the Texas Birth Defects Registry, a large, population-based birth defects registry. Data were evaluated for 563 non-syndromic cases with CAVC.
Results:
Significant associations were observed between non-syndromic CAVC in offspring and maternal pregestational diabetes (adjusted prevalence ratio (aPR) 6.74; 95% confidence interval (CI) 3.67, 12.37), gestational diabetes (aPR 1.69; 95% CI 1.03, 2.79) and obesity (aPR 1.69; 95% CI 1.24, 2.30).
Conclusions:
Our findings add non-syndromic CAVC to the growing list of birth defects that appear to be associated with maternal diabetes and obesity.
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