Brite J, Laughon S K, Troendle J, Mills J
1] Epidemiology Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA [2] Epidemiology and Biostatistics, CUNY School of Public Health at Hunter College, New York, NY, USA [3] CUNY Institute for Demographic Research (CIDR), New York, NY, USA.
Epidemiology Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
Int J Obes (Lond). 2014 Jun;38(6):878-82. doi: 10.1038/ijo.2013.244. Epub 2013 Dec 23.
Obesity is a risk factor for congenital heart defects (CHDs), but whether risk is independent of abnormal glucose metabolism remains unknown. Data on whether overweight status increases the risk are also conflicting.
We included 121 815 deliveries from a cohort study, the Consortium on Safe Labor (CSL), after excluding women with pregestational diabetes as recorded in the electronic medical record. CHD was identified via medical record discharge summaries. Adjusted odds ratios (ORs) for any CHD were calculated for prepregnancy body mass index (BMI) categories of overweight (25-<30 kg m(-2)), obese (30-<40 kg m(-2)) and morbidly obese (≥40 kg m(-2)) compared with normal weight (18.5-<25 kg m(-2)) women, and for specific CHD with obese groups combined (≥30 kg m(-2)). A subanalysis adjusting for oral glucose tolerance test (OGTT) results where available was performed as a proxy for potential abnormal glucose metabolism present at the time of organogenesis.
There were 1388 (1%) infants with CHD. Overweight (OR=1.15, 95% confidence interval (95% CI): 1.01-1.32), obese (OR=1.26, 95% CI: 1.09-1.44) and morbidly obese (OR=1.34, 95% CI: 1.02-1.76) women had greater OR of having a neonate with CHD than normal weight women (P<0.001 for trend). Obese women (BMI≥30 kg m(-2)) had higher OR of having an infant with conotruncal defects (OR = 1.33, 95% CI: (1.03–1.72) [corrected], atrial septal defects (OR=1.22, 95% CI: 1.04-1.43) and ventricular septal defects (OR=1.38, 95% CI: 1.06-1.79). Being obese remained a significant predictor of CHD risk after adjusting for OGTT.
Increasing maternal weight class was associated with an increased risk for CHD. In obese women, abnormal glucose metabolism did not completely explain the increased risk for CHD; the possibility that other obesity-related factors are teratogenic requires further investigation.
肥胖是先天性心脏病(CHD)的一个危险因素,但该风险是否独立于异常糖代谢尚不清楚。关于超重状态是否会增加风险的数据也存在矛盾。
我们纳入了一项队列研究——安全分娩联盟(CSL)中的121815例分娩病例,排除了电子病历中记录的孕前糖尿病女性。通过病历出院小结确定CHD。计算超重(25-<30 kg m(-2))、肥胖(30-<40 kg m(-2))和病态肥胖(≥40 kg m(-2))的孕前体重指数(BMI)类别与正常体重(18.5-<25 kg m(-2))女性相比患任何CHD的校正比值比(OR),以及肥胖组(≥30 kg m(-2))合并患特定CHD的校正比值比。对可用口服葡萄糖耐量试验(OGTT)结果进行校正的亚分析作为器官形成时潜在异常糖代谢的替代指标。
有1388例(1%)婴儿患有CHD。超重(OR=1.15,95%置信区间(95%CI):1.01-1.32)、肥胖(OR=1.26,95%CI:1.09-1.44)和病态肥胖(OR=1.34,95%CI:1.02-1.76)的女性比正常体重女性生育患CHD新生儿的OR更高(趋势P<0.001)。肥胖女性(BMI≥30 kg m(-2))生育患圆锥干畸形(OR = 1.33,95%CI:(1.03–1.72) [校正])、房间隔缺损(OR=1.22,95%CI:1.04-1.43)和室间隔缺损(OR=1.38,95%CI:1.06-1.79)婴儿的OR更高。校正OGTT后,肥胖仍然是CHD风险的显著预测因素。
孕妇体重类别增加与CHD风险增加相关。在肥胖女性中,异常糖代谢并不能完全解释CHD风险增加;其他与肥胖相关的因素具有致畸性的可能性需要进一步研究。