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Maternal Body Mass Index and Risk of Congenital Heart Defects in Infants: A Dose-Response Meta-Analysis

机译:婴幼儿母体体重指数和先天性心脏缺陷的风险:剂量 - 反应元分析

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摘要

Objective. The exact shape of the dose-response relationship between maternal body mass index (BMI) and the risk of congenital heart defects (CHDs) in infants has not been clearly defined yet. This study aims to further clarify the relationship between maternal obesity and the risk of CHDs in infants by an overall and dose-response meta-analysis. Methods. PubMed, Embase, and Web of Science databases were searched to identify all related studies. The studies were limited to human cohort or case-control studies in English language. Random-effect models and dose-response meta-analysis were used to synthesize the results. Heterogeneity, subgroup analysis, sensitivity analysis, and publication bias were also assessed. Results. Nineteen studies with 2,416,546 participants were included in our meta-analysis. Compared with the mothers with normal weight, the pooled relative risks (RRs) of infants with CHDs were 1.08 (95% CI=1.03-1.13) in overweight and 1.23 (95% CI=1.17-1.29) in obese mothers. According to the findings from the linear meta-analysis, we observed an increased risk of infants with CHDs (RR=1.07, 95% CI=1.06-1.08) for each 5 kg/m2 increase in maternal BMI. A nonlinear relationship between maternal BMI and risk of infants with CHDs was also found (p=0.012). Conclusion. The results from our meta-analysis indicate that increased maternal BMI is related to increased risk of CHDs in infants.
机译:客观的。孕妇体体重指数(BMI)与婴儿中先天性心脏缺陷(CHD)的风险的确切形状尚未明确定义。本研究旨在进一步阐明母体肥胖症与婴儿CHD风险的关系,通过整体和剂量 - 反应荟萃分析。方法。搜索PubMed,Embase和科学数据库网络,以确定所有相关的研究。这些研究仅限于英语的人群或病例对照研究。随机效应模型和剂量反应META分析用于合成结果。还评估了异质性,亚组分析,敏感性分析和出版物偏见。结果。 19项研究与2,416,546名参与者纳入我们的荟萃分析中。与具有正常体重的母亲相比,在肥胖的母亲中,患有CHD的婴儿的汇集相对风险(RRS)婴儿的婴儿的汇集相对风险(RRS)是1.08(95%CI = 1.03-1.13),1.23(95%CI = 1.17-1.29)。根据线性Meta分析的发现,我们观察到每次5kg / m 2增加母体BMI的CHDS(RR = 1.07,95%CI = 1.06-1.08)的婴儿的风险增加。还发现了母体BMI之间的非线性关系以及CHDS的婴儿的风险(p = 0.012)。结论。我们的Meta分析的结果表明,增加的母体BMI与婴儿CHD的风险增加有关。

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