Yim Hyung Eun, Bae In Sun, Yoo Kee Hwan, Hong Young Sook, Lee Joo Won
Department of Pediatrics, College of Medicine, Korea University, Seoul, 152-703, Korea.
Pediatr Res. 2007 Aug;62(2):183-7. doi: 10.1203/PDR.0b013e31809871f1.
We investigated whether genetic polymorphisms of vascular endothelial growth factor (VEGF) and transforming growth factor-beta1 (TGF-beta1), potential candidate genes in the pathogenesis of urinary tract infection (UTI) and vesicoureteral reflux (VUR), are associated with the susceptibility to UTI and VUR, and renal scarring. We recruited 89 controls and 86 UTI and 58 VUR children. The UTI group was subdivided into two groups according to renal scarring. Two polymorphisms of VEGF and three of TGF-beta1 genes were investigated by using PCR-restriction fragment length polymorphism analysis. In both UTI and VUR groups, there was an increase in frequency of the VEGF -460 CC (control, 4.3; UTI, 15.9; VUR, 17.8%; p < 0.05), TGF-beta1 -509 CC (control, 8.7; UTI, 34.6; VUR, 35.1%; p < 0.001), and TGF-beta1 -800 GG genotypes (control, 19.1; UTI, 40.5; VUR, 40.4%; p < 0.05). An increase in the TGF-beta1 +869 CC (scar-positive, 35.4; scar-negative, 10.3%; p < 0.05) and a decrease in the +869 TC genotype (scar-positive, 29.2; scar-negative, 55.2%; p < 0.05) were observed in the scar-positive subjects. There were no differences in +405 VEGF genotype frequencies. The VEGF T-460C and the TGF-beta1 C-509T, G-800A, and T869C polymorphisms could be genetic markers of the process of UTI and VUR.
我们研究了血管内皮生长因子(VEGF)和转化生长因子-β1(TGF-β1)的基因多态性,这两个基因是尿路感染(UTI)和膀胱输尿管反流(VUR)发病机制中的潜在候选基因,是否与UTI、VUR的易感性以及肾瘢痕形成有关。我们招募了89名对照儿童、86名UTI儿童和58名VUR儿童。UTI组根据肾瘢痕形成情况分为两组。采用聚合酶链反应-限制性片段长度多态性分析研究了VEGF的两个多态性和TGF-β1基因的三个多态性。在UTI组和VUR组中,VEGF -460 CC基因型(对照组,4.3%;UTI组,15.9%;VUR组,17.8%;p<0.05)、TGF-β1 -509 CC基因型(对照组,8.7%;UTI组,34.6%;VUR组,35.1%;p<0.001)以及TGF-β1 -800 GG基因型(对照组,19.1%;UTI组,40.5%;VUR组,40.4%;p<0.05)的频率均增加。在有肾瘢痕的受试者中,观察到TGF-β1 +869 CC基因型增加(瘢痕阳性组,35.4%;瘢痕阴性组,10.3%;p<0.05),而+869 TC基因型减少(瘢痕阳性组,29.2%;瘢痕阴性组,55.2%;p<0.05)。+405 VEGF基因型频率无差异。VEGF T-460C以及TGF-β1 C-509T、G-800A和T869C多态性可能是UTI和VUR发病过程的遗传标志物。