Vitamin D Receptor Gene Alw I, Fok I, Apa I, and Taq I Polymorphisms in Patients With Urinary Stone

被引:19
作者
Seo, Ill Young [1 ]
Kang, In-Hong
Chae, Soo-Cheon
Park, Seung Chol
Lee, Young-Jin
Yang, Yun Sik
Ryu, Soo Bang
Rim, Joung Sik
机构
[1] Wonkwang Univ, Sch Med, Dept Urol, Iksan 570180, Jeonbuk, South Korea
关键词
BONE-MINERAL DENSITY; TRANSLATION INITIATION SITE; START CODON; CALCIUM NEPHROLITHIASIS; ASSOCIATION; UROLITHIASIS; DISEASE; CHILDREN; WOMEN;
D O I
10.1016/j.urology.2009.10.006
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
OBJECTIVES the candidate genes associated with urinary stones. Urinary stones are a multifactorial disease that includes various genetic factors. METHODS A normal control group of 535 healthy subjects and 278 patients with urinary stones was evaluated. Of 125 patients who presented stone samples, 102 had calcium stones on chemical analysis. The VDR gene Alw I, Fok I, Apa I, and Taq I polymorphisms were evaluated using the polymerase chain reaction-restriction fragment length polymorphism analysis. Allelic and genotypic frequencies were calculated to identify associations in both groups. The haplotype frequencies of the VDR gene polymorphisms for multiple loci were also determined. RESULTS For the VDR gene Alw I, Fok I, Apa I, and Taq I polymorphisms, there was no statistically significant difference between the patients with urinary stones and the healthy controls. There was also no statistically significant difference between the patients with calcium stones and the healthy controls. A novel haplotype (Ht 4; CTTT) was identified in 13.5% of the patients with urinary stones and in 8.3% of the controls (P = .001). The haplotype frequencies were significantly different between the patients with calcium stones and the controls (P = .004). CONCLUSIONS The VDR gene Alw I, Fok I, Apa I, and Taq I polymorphisms does not seem to be candidate genetic markers for urinary stones in Korean patients. However, 1 novel haplotype of the VDR gene polymorphisms for multiple loci might be a candidate genetic marker. UROLOGY 75: 923-927, 2010. (C) 2010 Elsevier Inc.
引用
收藏
页码:923 / 927
页数:5
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