Gambhir L, Höller T, Müller M, Schott G, Vogt H, Detlefsen B, Ebert A-K, Fisch M, Beaudoin S, Stein R, Boyadjiev S A, Gearhart J P, Rösch W, Utsch B, Boemers T M, Reutter H, Ludwig M
Department of Clinical Biochemistry and Clinical Pharmacology, University of Bonn, Bonn, Germany.
J Urol. 2008 Apr;179(4):1539-43. doi: 10.1016/j.juro.2007.11.092. Epub 2008 Mar 4.
We sought to identify causative nongenetic and genetic risk factors for the bladder exstrophy-epispadias complex.
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.
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).
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.
我们试图确定膀胱外翻-尿道上裂综合征的非遗传和遗传致病危险因素。
共邀请了237个患有膀胱外翻-尿道上裂综合征的家庭参与研究,主要从欧洲国家的214个家庭获取了信息。
两个家庭显示出家族性发病情况。在包括尿道上裂、典型膀胱外翻和泄殖腔外翻的所有亚组中均发现男性占优势,男性与女性的比例分别为1.4:1、2.8:1和2.0:1(p = 0.001)。未发现与父母年龄、母亲生育史或受孕前后母亲接触酒精、药物、化学毒物、辐射或感染有关。然而,受孕前后母亲吸烟在泄殖腔外翻患者中比在尿道上裂/典型膀胱外翻患者的合并组中更为常见(p = 0.009)。只有16.8%的母亲遵循了目前关于受孕前后补充叶酸的建议,17.6%的母亲在妊娠10周前开始补充。有趣的是,在后一组中,泄殖腔外翻患者的母亲比尿道上裂/典型膀胱外翻患者合并组的母亲更遵守叶酸补充规定(p = 0.037)。此外,泄殖腔外翻患儿的母亲在产前比尿道上裂/典型膀胱外翻患儿的母亲更常知道自己的孩子会有先天性畸形(p <0.0001)。
我们的研究证实了以下假设,即尿道上裂、典型膀胱外翻和泄殖腔外翻存在因果关系,代表了同一发育缺陷的一系列表现,家族内复发风险较小。胚胎期暴露于母亲吸烟似乎会加重病情,而受孕前后补充叶酸似乎并不能缓解病情。严重和轻度表型之间的产前超声检测率不成比例,可能是由于在关注神经管缺陷时忽视了对全膀胱的成像。