Abstract

This study aimed to examine effect modification of maternal risk factor exposures and congenital heart disease (CHD) by maternal folic acid supplementation (FAS)/non-FAS. We included 8379 CHD cases and 6918 CHD-free controls from 40 clinical centers in Guangdong Province, Southern China, 2004–2016. Controls were randomly chosen from malformation-free fetuses and infants and frequency matched to the echocardiogram-confirmed cases by enrollment hospital and year of birth. We used multiple regression models to evaluate interactions between FAS/non-FAS and risk factors on CHDs and major CHD categories, adjusted for confounding variables. We detected statistically significant additive and multiplicative interactions between maternal FAS/non-FAS and first-trimester fever, viral infection, and threatened abortion on CHDs. An additive interaction on CHDs was also identified between non-FAS and living in a newly renovated home. We observed a statistically significant dose-response relationship between non-FAS and a greater number of maternal risk factors on CHDs. Non-FAS and maternal risk factors interacted additively on multiple critical CHDs, conotruncal defects, and right ventricular outflow tract obstruction. Maternal risk factor exposures may have differential associations with CHD risk in offspring, according to FAS. These findings may inform the design of targeted interventions to prevent CHDs in highly susceptible population groups.

Highlights

  • Congenital heart diseases (CHDs) rank first among birth defects worldwide and affect approximately 1% of all live births [1]

  • After adjustment for covariates, first-trimester maternal folic acid supplementation (FAS) was associated with a lower risk of CHDs in offspring (OR = 0.69, 95% confidence interval (CI): 0.62–0.76)

  • Among the statistically significant additive interactions, we found the greatest risk of CHD among offspring among non-FAS mothers exposed to first-trimester viral infection (OR = 4.73, 95% CI: 3.85–5.80)

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Summary

Introduction

Congenital heart diseases (CHDs) rank first among birth defects worldwide and affect approximately 1% of all live births [1]. Burden of Disease Study, more than 11 million individuals live with CHDs globally, and CHDs have caused approximately 89 thousand years lived with a disability [4]. This impact implies a tremendous economic burden for both the affected families and society as a whole. The etiology of CHDs is multifactorial, consisting of both genetic and environmental factors. There have been major breakthroughs in understanding the inherited causes of CHDs over the past 50 years, including the identification of specific genetic abnormalities for selected CHD phenotypes [6,7].

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