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妊娠期酒精使用诊断编码与后代圆锥干及心内膜垫心脏缺陷的关联。

Association of Alcohol Use Diagnostic Codes in Pregnancy and Offspring Conotruncal and Endocardial Cushion Heart Defects.

机构信息

Department of Surgery Keck School of Medicine of University of Southern California Los Angeles CA.

Department of Pediatrics and Herbert Wertheim School of Public Health and Longevity Science University of California San Diego La Jolla CA.

出版信息

J Am Heart Assoc. 2022 Jan 18;11(2):e022175. doi: 10.1161/JAHA.121.022175. Epub 2022 Jan 11.

DOI:10.1161/JAHA.121.022175
PMID:35014860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9238516/
Abstract

Background The pathogenesis of congenital heart disease (CHD) remains largely unknown, with only a small percentage explained solely by genetic causes. Modifiable environmental risk factors, such as alcohol, are suggested to play an important role in CHD pathogenesis. We sought to evaluate the association between prenatal alcohol exposure and CHD to gain insight into which components of cardiac development may be most vulnerable to the teratogenic effects of alcohol. Methods and Results This was a retrospective analysis of hospital discharge records from the California Office of Statewide Health Planning and Development and linked birth certificate records restricted to singleton, live-born infants from 2005 to 2017. Of the 5 820 961 births included, 16 953 had an alcohol-related code during pregnancy. Log linear regression was used to calculate risk ratios (RR) for CHD among individuals with an alcohol-related code during pregnancy versus those without. Three models were created: (1) unadjusted, (2) adjusted for maternal demographic factors, and (3) adjusted for maternal demographic factors and comorbidities. Maternal alcohol-related code was associated with an increased risk for CHD in all models (RR, 1.33 to 1.84); conotruncal (RR, 1.62 to 2.11) and endocardial cushion (RR, 2.71 to 3.59) defects were individually associated with elevated risk in all models. Conclusions Alcohol-related diagnostic codes in pregnancy were associated with an increased risk of an offspring with a CHD, with a particular risk for endocardial cushion and conotruncal defects. The mechanistic basis for this phenotypic enrichment requires further investigation.

摘要

背景

先天性心脏病(CHD)的发病机制在很大程度上仍然未知,仅有一小部分可以仅归因于遗传原因。可改变的环境风险因素,如酒精,被认为在 CHD 的发病机制中起着重要作用。我们试图评估产前酒精暴露与 CHD 之间的关联,以深入了解心脏发育的哪些成分可能最容易受到酒精的致畸作用的影响。

方法和结果

这是对加利福尼亚州全州卫生规划与发展办公室的医院出院记录和 2005 年至 2017 年的链接出生证明记录进行的回顾性分析,仅限于单胎、活产婴儿。在包括的 5820961 例分娩中,有 16953 例在怀孕期间有与酒精相关的 代码。对数线性回归用于计算怀孕期间有与酒精相关的 代码的个体与没有的个体之间 CHD 的风险比(RR)。创建了三个模型:(1)未调整,(2)调整了母亲的人口统计学因素,以及(3)调整了母亲的人口统计学因素和合并症。在所有模型中,母亲的酒精相关代码与 CHD 的风险增加相关(RR,1.33 至 1.84);圆锥动脉干(RR,1.62 至 2.11)和心内膜垫(RR,2.71 至 3.59)缺陷在所有模型中均与风险升高相关。

结论

怀孕期间与酒精相关的诊断代码与后代 CHD 的风险增加相关,与心内膜垫和圆锥动脉干缺陷的风险特别相关。这种表型富集的机制基础需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd32/9238516/bf1638e7396e/JAH3-11-e022175-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd32/9238516/6af87dbbc91d/JAH3-11-e022175-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd32/9238516/bf1638e7396e/JAH3-11-e022175-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd32/9238516/6af87dbbc91d/JAH3-11-e022175-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd32/9238516/bf1638e7396e/JAH3-11-e022175-g001.jpg

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