Akin Yasemin, Ercan Oya, Telatar Berrin, Tarhan Fatih, Comert Serdar
Departments of Pediatrics IUrology I, Dr Lütfi Kırdar Kartal Training and Research HospitalDivisions of Pediatric Endocrinology and Adolescent Medicine, Cerrahpaşa Medical Faculty of Istanbul University, Istanbul, Turkey.
Pediatr Int. 2011 Oct;53(5):754-760. doi: 10.1111/j.1442-200X.2011.03340.x.
The aim of the present prospective study was to determine the incidence of hypospadias in newborns in one of the busiest teaching hospitals of Istanbul, and to investigate the risk factors.
All live-born boys delivered between September 2007 and December 2008 were screened for hypospadias. A questionnaire was given to the parents of the hypospadias and control subjects for investigation.
Out of 1750 boys examined, 34 had hypospadias, that is, the frequency was 19.4 per 1000 male live-births and 93.7 per 10,000 total live-born deliveries. The incidence of additional coexistent anomalies was 29.4%, predominantly urogenital (17.6%), the majority of which were cryptorchidism (14.7%). Twelve (35.3%) of the 34 hypospadiac boys had a second family member with a genital anomaly, nine (26.5%) of whom had hypospadias, three (8.8%) being the fathers. Mean birthweight, length and head circumference were significantly lower in the hypospadiac infants than the control group (P= 0.003, P= 0.025, P= 0.002). Although parity, parental consanguinity, hypospadias in family members, and low birthweight also varied significantly among the groups, logistic regression analysis indicated that maternal age, prematurity, coexistence of cryptorchidism and presence of genital anomaly among family members were independent risk factors for hypospadias (P= 0.016, P= 0.0001, P= 0.041, P= 0.0001, respectively).
Genetic predisposition and placental insufficiency in early gestation might play a role in the etiology of hypospadias.
本前瞻性研究的目的是确定伊斯坦布尔最繁忙的教学医院之一新生儿尿道下裂的发病率,并调查相关危险因素。
对2007年9月至2008年12月间出生的所有活产男婴进行尿道下裂筛查。向尿道下裂患儿及对照组患儿的父母发放问卷进行调查。
在1750名接受检查的男婴中,有34例患有尿道下裂,即发病率为每1000例男性活产儿中有19.4例,每10000例总活产儿中有93.7例。合并其他异常的发生率为29.4%,主要为泌尿生殖系统异常(17.6%),其中大多数为隐睾症(14.7%)。34例尿道下裂男童中有12例(35.3%)有第二位家庭成员患有生殖器异常,其中9例(26.5%)患有尿道下裂,3例(8.8%)为父亲。尿道下裂患儿的平均出生体重、身长和头围显著低于对照组(P = 0.003、P = 0.025、P = 0.002)。尽管各组间的产次、父母近亲结婚、家庭成员尿道下裂情况及低出生体重也有显著差异,但逻辑回归分析表明,母亲年龄、早产、隐睾症合并存在及家庭成员生殖器异常是尿道下裂的独立危险因素(分别为P = 0.016、P = 0.0001、P = 0.041、P = 0.0001)。
遗传易感性和妊娠早期胎盘功能不全可能在尿道下裂的病因中起作用。