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Epidemiological survey of 214 families with bladder exstrophy-epispadias complex.

机译:214例膀胱​​外生上皮增生综合症的流行病学调查。

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PURPOSE: We sought to identify causative nongenetic and genetic risk factors for the bladder exstrophy-epispadias complex. MATERIALS AND METHODS: A total of 237 families with the bladder exstrophy-epispadias complex were invited to participate in the study, and information was obtained from 214 families, mainly from European countries. RESULTS: Two families showed familial occurrence. Male predominance was found among all subgroups comprising epispadias, classic bladder exstrophy and cloacal exstrophy, with male-to-female ratios of 1.4:1, 2.8:1 and 2.0:1, respectively (p = 0.001). No association with parental age, maternal reproductive history or periconceptional maternal exposure to alcohol, drugs, chemical noxae, radiation or infections was found. However, periconceptional maternal exposure to smoking was significantly more common in patients with cloacal exstrophy than in the combined group of patients with epispadias/classic bladder exstrophy (p = 0.009). Only 16.8% of mothers followed the current recommendations of periconceptional folic acid supplementation, and 17.6% had started supplementation before 10 weeks of gestation. Interestingly, in the latter group mothers of patients with cloacal exstrophy were more compliant with folic acid supplementation than were mothers of the combined group of patients with epispadias/classic bladder exstrophy (p = 0.037). Furthermore, mothers of children with cloacal exstrophy knew significantly more often prenatally that their child would have a congenital malformation than did mothers of children with epispadias/classic bladder exstrophy (p <0.0001). CONCLUSIONS: Our study corroborates the hypothesis that epispadias, classic bladder exstrophy and cloacal exstrophy are causally related, representing a spectrum of the same developmental defect, with a small risk of recurrence within families. Embryonic exposure to maternal smoking appears to enforce the severity, whereas periconceptional folic acid supplementation does not seem to alleviate it. There is a disproportional prenatal ultrasound detection rate between severe and mild phenotypes, possibly due to the neglect of imaging of full bladders with a focus on neural tube defects.
机译:目的:我们试图找出导致膀胱萎缩-上睑下垂复合体的非遗传和遗传危险因素。材料与方法:共邀请237个患有膀胱萎缩症-上睑外翻复合体的家庭参加该研究,并从214个主要来自欧洲国家的家庭中获得了信息。结果:两个家庭显示出家族性发生。在包括尿道上裂,经典膀胱萎缩症和泄殖腔萎缩症的所有亚组中发现了男性优势,男女比例分别为1.4:1、2.8:1和2.0:1(p = 0.001)。未发现与父母的年龄,孕产妇的生殖史或围产期的母亲暴露于酒精,毒品,化学物质,辐射或感染有关。然而,泄殖腔营养不良患者的围产期母体吸烟明显高于尿道上裂/经典膀胱营养不良合并患者(p = 0.009)。只有16.8%的母亲遵循目前的建议进行围孕期叶酸补充,而17.6%的母亲在妊娠10周之前开始补充叶酸。有趣的是,在后一组中,泄殖腔外溢患者的母亲比上尿道上裂/经典性膀胱外翻合并患者的母亲对叶酸补充的依从性更高(p = 0.037)。此外,患有泄殖腔营养不良的儿童的母亲比患有尿道上裂/经典膀胱营养不良的儿童的母亲在产前更频繁地知道他们的孩子患有先天性畸形(p <0.0001)。结论:我们的研究证实了尿道上裂,经典膀胱萎缩症和泄殖腔萎缩症有因果关系的假说,代表了一系列相同的发育缺陷,家庭内复发的风险很小。胚胎暴露于孕妇吸烟似乎会加剧病情的严重性,而围孕期补充叶酸似乎并不能缓解这种情况。重度和轻度表型之间的产前超声检测率不成比例,可能是由于忽略了全膀胱成像,而侧重于神经管缺陷。

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