Zhu Yong, Romitti Paul A, Caspers Conway Kristin M, Shen Dereck H, Sun Lixian, Browne Marilyn L, Botto Lorenzo D, Lin Angela E, Druschel Charlotte M
Department of Epidemiology, The University of Iowa, Iowa City, Iowa.
New York State Department of Health, Albany, New York.
Birth Defects Res A Clin Mol Teratol. 2015 Jul;103(7):617-29. doi: 10.1002/bdra.23352. Epub 2015 Jun 27.
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.
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.
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.
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.
先天性心脏病(CHD)是出生缺陷导致婴儿死亡的主要原因。动物研究表明,子宫内酒精暴露是心脏发生的致畸剂;然而,流行病学研究的结果却不一致。
利用国家出生缺陷预防研究的数据,估计1997年至2007年期间,先天性心脏病与病例组(n = 7076)和对照组(n = 7972)母亲报告的受孕前(怀孕前1个月至孕早期)酒精摄入量以及预期分娩日期之间的关联。按类别(圆锥动脉干、间隔、左心室流出道梗阻、右心室流出道梗阻、合并先天性心脏病的内脏异位)和亚型(如法洛四联症[TOF])检查先天性心脏病。所检查的酒精摄入量指标包括是否饮酒、每月最大平均饮酒量、暴饮以及酒精类型。使用无条件逻辑回归分析估计调整后的比值比和95%置信区间。
观察到法洛四联症以及所检查的每项母亲酒精摄入量指标、右心室流出道梗阻、合并先天性心脏病的内脏异位和饮用蒸馏酒的风险增加,尽管在统计学上仅略有显著意义。在几个先天性心脏病类别(间隔缺损、左心室流出道梗阻和右心室流出道梗阻)以及一些相应亚型中,观察到不同酒精摄入量指标的风险显著降低。在所检查的其他先天性心脏病中未观察到显著风险。
对这个大型、定义明确的研究样本的分析未显示母亲酒精摄入量指标与所检查的大多数先天性心脏病之间存在统计学上显著增加的风险。这些发现可能部分反映了回顾性暴露评估或未测量混杂因素的局限性。建议进一步开展研究,持续改进酒精摄入量的测量方法。