Association of transforming growth factor-β1 gene polymorphism with familial Vesicoureteral reflux

被引:8
作者
Kuroda, Seika
Solari, Valeria
Puri, Prent [1 ]
机构
[1] Our Ladys Hosp Sick Children, Childrens Res Ctr, Dublin 12, Ireland
[2] Natl Childrens Hosp, Dublin, Ireland
关键词
bladder; ureter; polymorphism; genetic; vesico-ureteral reflux; transforming growth factor beta;
D O I
10.1016/j.juro.2007.03.199
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: Familial clustering of vesicoureteral reflux suggests that genetic factors have an important role in the pathogenesis of vesicoureteral reflux. Transforming growth factor-beta 1 is a multifunctional peptide that controls proliferation and differentiation in many cell types. Recently an association between the transforming growth factor-beta 1 -509 and +869 gene polymorphism, and renal parenchymal scarring was reported. We investigated the genetic contribution of transforming growth factor-beta 1 in familial vesicoureteral reflux by examining the genotype frequencies of transforming growth factor-beta 1 polymorphic variants. Materials and Methods: The study included 141 families in which I or more siblings had primary vesicoureteral reflux. Renal parenchymal scarring was assessed using dimercapto-succinic acid scans. Genotyping was performed in 280 patients with vesicoureteral reflux, including 133 index patients and 147 siblings, and in 74 controls for the position -509 and the coding region at position 10 (+869) of the transforming growth factor-PI gene polymorphism by polymerase chain reaction, gel analysis and appropriate restriction digest. Results: The genotype frequency of -509CC was significantly increased in the familial vesicoureteral reflux group compared to controls (58% vs 33%, p < 0.01), whereas -509TT genotype frequency was significantly lower in the familial vesicoureteral reflux group compared to controls (7.5% vs 28%, p < 0.01). Similarly there was a significant increase in the +869TT genotype (52% vs 32%, p < 0.05), while the +869CC genotype was significantly lower in patients with familial vesicoureteral reflux compared to controls (11% vs 24%, p < 0.01). There were no significant differences in transforming growth factor-beta 1. genotype distribution between patients with vesicoureteral reflux with and without renal parenchymal scarring. Conclusions: To our knowledge this study demonstrates for the first time the association of the cytokine transforming growth factor-beta 1 gene polymorphism in patients with familial vesicoureteral reflux. Individuals with the transforming growth factor-beta 1 -509CC and 869TT genotype may have increased susceptibility to vesicoureteral reflux.
引用
收藏
页码:1650 / 1653
页数:4
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