Birth Defects Research Part A Clinical and Molecular Teratology, volume 103, issue 7, pages 617-629
Maternal periconceptional alcohol consumption and congenital heart defects
Yong Zhu
1
,
Paul A. Romitti
1
,
Kristin M Caspers Conway
1
,
Dereck H Shen
1
,
Lixian Sun
1
,
Marilyn L. Browne
2, 3
,
Lorenzo D. Botto
4
,
Angela E. Lin
5
,
Charlotte M. Druschel
2, 3
2
New York State Department of Health; Albany New York
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Publication type: Journal Article
Publication date: 2015-06-27
SJR: —
CiteScore: —
Impact factor: —
ISSN: 15420752, 15420760
PubMed ID:
26118863
General Medicine
Developmental Biology
Embryology
Pediatrics, Perinatology and Child Health
Abstract
Background Congenital heart defects (CHDs) are the leading cause of infant death from birth defects. Animal studies suggest in utero alcohol exposure is a teratogen for cardiogenesis; however, results from epidemiologic studies are mixed. Methods Data from the National Birth Defects Prevention Study were used to estimate associations between CHDs and case (n = 7076) and control (n = 7972) mother reports of periconceptional (1 month before pregnancy through the first trimester) alcohol consumption with expected delivery dates during 1997 to 2007. CHDs were examined by category (conotruncal, septal, left ventricular outflow tract obstruction, and right ventricular outflow tract obstruction, heterotaxy with CHD) and subtype (e.g., tetralogy of Fallot [TOF]). Alcohol measures examined were any consumption, maximum average drinks per month, binge drinking, and alcohol type. Adjusted odds ratios and 95% confidence intervals were estimated using unconditional logistic regression analysis. Results Increased risks, albeit marginally statistically significant, were observed for TOF and each maternal alcohol measure examined and for right ventricular outflow tract obstruction and heterotaxy with CHD and consumption of distilled spirits. Significantly reduced risks were observed for several CHD categories (septal defects, left ventricular outflow tract obstruction, and right ventricular outflow tract obstruction) and some corresponding subtypes with different alcohol measures. Significant risks were not observed for the other CHDs examined. Conclusion Analysis of this large, well-defined study sample did not show statistically significant increased risks between measures of maternal alcohol consumption and most CHDs examined. These findings may reflect, in part, limitations with retrospective exposure assessment or unmeasured confounders. Additional studies with continued improvement in measurement of alcohol consumption are recommended.
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