Keppler-Noreuil Kim M, Conway Kristin M, Shen Dereck, Rhoads Anthony J, Carey John C, Romitti Paul A
Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa.
Am J Med Genet A. 2017 Nov;173(11):2873-2885. doi: 10.1002/ajmg.a.38469. Epub 2017 Sep 28.
Cloacal exstrophy (CE) and persistent cloaca (PC) (alternatively termed urorectal septum malformation sequence [URSMS]), represent two major cloacal defects (CDs). Clinical characteristics and risk factors often are studied for both defects combined, rather than exploring if these defects have different etiologies. We enumerated clinical features for 47 CE and 54 PC (inclusive of URSMS) cases from the National Birth Defects Prevention Study. Thirty-three CE cases were classified as isolated and 14 as multiple (presence of unassociated major defects); respective totals for PC cases were 26 and 28. We compared selected child and maternal characteristics between 11,829 non-malformed controls and CE and PC cases using chi-square or Fisher's exact tests. Compared to controls, CE and PC cases were statistically more likely (p < 0.05) to be preterm; CE cases were more likely to be multiple births. We conducted logistic regression analysis to estimate odds ratios and 95% confidence intervals for any CD, CE, and PC with selected self-reported maternal prepregnancy and periconceptional (one month prior to 3 months following conception) exposures. In crude and adjusted analyses, we observed significant positive associations for any CD, CE, and PC with use of any fertility medication or assisted reproductive technology procedure. Significant positive associations observed only in crude analyses were any CD with maternal obesity or use of progesterone, any CD and CE with any x-ray, and any CD and PC with use of folate antagonist medications. Our findings provide some of the first insights into potential differing etiologies for CE and PC.
泄殖腔外翻(CE)和泄殖腔存留(PC)(也称为尿直肠隔畸形序列[URSMS]),是两种主要的泄殖腔缺陷(CDs)。临床特征和风险因素通常是针对这两种缺陷合并进行研究,而不是探究这些缺陷是否有不同的病因。我们从国家出生缺陷预防研究中列举了47例CE和54例PC(包括URSMS)病例的临床特征。33例CE病例被分类为孤立性,14例为多发性(存在不相关的主要缺陷);PC病例的相应总数分别为26例和28例。我们使用卡方检验或费舍尔精确检验,比较了11829例非畸形对照与CE和PC病例之间选定的儿童和母亲特征。与对照组相比,CE和PC病例在统计学上更有可能早产(p < 0.05);CE病例更有可能是多胞胎。我们进行了逻辑回归分析,以估计任何CD、CE和PC与选定的自我报告的母亲孕前和受孕前(受孕前1个月至受孕后3个月)暴露因素的比值比和95%置信区间。在粗分析和调整分析中,我们观察到任何CD、CE和PC与使用任何生育药物或辅助生殖技术程序之间存在显著的正相关。仅在粗分析中观察到的显著正相关包括任何CD与母亲肥胖或使用孕酮、任何CD和CE与任何X光检查,以及任何CD和PC与使用叶酸拮抗剂药物。我们的研究结果为CE和PC潜在的不同病因提供了一些初步见解。