Khalilipalandi Sara, Lemieux Alyssia, Lauzon-Schnittka Jonathan, Perreault Laurence, Dubois Mélodie, Tousignant Angélique, Watelle Laurence, Pratte Gabriel, Dallaire Frédéric
Faculty of Medicine and Health Sciences, Université de Sherbrooke and Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebéc, Canada.
Faculty of Medicine and Health Sciences, Université de Sherbrooke and Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebéc, Canada.
Can J Cardiol. 2024 Dec;40(12):2476-2495. doi: 10.1016/j.cjca.2024.07.004. Epub 2024 Jul 10.
There is considerable heterogeneity in studies on prenatal risk factors for congenital heart diseases (CHDs). We performed a meta-analysis of all nongenetic factors of CHDs. This report presents results of factors related to maternal chronic diseases and parental exposures.
A systematic search encompassing concepts of CHD and risk factors was used, using the following inclusion criteria: (1) original peer-reviewed articles, (2) quantifying the effects of risk factors for CHDs, (3) between 1989 and 2022. Pooled odds ratios (ORs) and 95% confidence interval (CI) were calculated using a random-effect model.
Inclusion criteria were met for 170 studies. There was an association between being overweight or obese and CHDs (OR, 1.26; 95% CI, 1.15-1.37), with a dose-effect relationship. Pregestational diabetes (PGDM) was associated with CHDs (OR, 3.51; 95% CI, 2.86-4.3), without difference between type 1 and type 2 PGDM. The effect size of gestational diabetes was less than that of PGDM (OR, 1.38; 95% CI, 1.18-1.61). There was an association between CHDs and pre-eclampsia (OR, 2.01; 95% CI, 1.32-3.05), paternal smoking (OR, 1.32; 95% CI, 1.03-1.70), and alcohol use (OR, 1.50; 95% CI, 1.08-2.08). A smaller association was found with maternal smoking and advanced maternal age.
There exists robust evidence for increased risk of CHD in the presence of obesity, maternal diabetes, maternal smoking, and increased maternal age. The effect sizes were relatively modest, except for PGDM. The robustness of the evidence decreased when CHDs were divided into subgroups or when the analyses were restricted to severe CHDs.
先天性心脏病(CHD)产前危险因素的研究存在相当大的异质性。我们对CHD的所有非遗传因素进行了荟萃分析。本报告展示了与母亲慢性病和父母暴露相关因素的研究结果。
采用系统检索,涵盖CHD和危险因素的概念,使用以下纳入标准:(1)经同行评审的原始文章;(2)量化CHD危险因素的影响;(3)1989年至2022年期间。使用随机效应模型计算合并比值比(OR)和95%置信区间(CI)。
170项研究符合纳入标准。超重或肥胖与CHD之间存在关联(OR,1.26;95%CI,1.15 - 1.37),呈剂量效应关系。孕前糖尿病(PGDM)与CHD相关(OR,3.51;95%CI,2.86 - 4.3),1型和2型PGDM之间无差异。妊娠期糖尿病的效应大小小于PGDM(OR,1.38;95%CI,1.18 - 1.61)。CHD与子痫前期(OR,2.01;95%CI,1.32 - 3.05)、父亲吸烟(OR,1.32;95%CI,1.03 - 1.70)以及饮酒(OR,1.50;95%CI,1.08 - 2.08)之间存在关联。母亲吸烟和母亲高龄与之的关联较小。
有充分证据表明,肥胖、母亲糖尿病、母亲吸烟和母亲年龄增加会增加患CHD的风险。除PGDM外,效应大小相对较小。当将CHD分为亚组或分析仅限于严重CHD时,证据的稳健性降低。