Suppr超能文献

维生素 D 受体基因 AlwI、FokI、ApaI 和 TaqI 多态性与尿路结石患者的关系。

Vitamin D receptor gene Alw I, Fok I, Apa I, and Taq I polymorphisms in patients with urinary stone.

机构信息

Department of Urology, Wonkwang University School of Medicine, Iksan, Jeonbuk, Korea.

出版信息

Urology. 2010 Apr;75(4):923-7. doi: 10.1016/j.urology.2009.10.006.

Abstract

OBJECTIVES

To evaluate vitamin D receptor (VDR) gene polymorphisms in Korean patients so as to identify 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.

摘要

目的

评估韩国患者维生素 D 受体(VDR)基因多态性,以鉴定与尿石症相关的候选基因。尿石症是一种多因素疾病,包括多种遗传因素。

方法

评估了 535 名健康对照者和 278 名尿路结石患者的正常对照组。在 125 名提供结石样本的患者中,有 102 名经化学分析为钙结石。采用聚合酶链反应-限制性片段长度多态性分析评估 VDR 基因 Alw I、Fok I、Apa I 和 Taq I 多态性。计算等位基因和基因型频率,以鉴定两组之间的关联。还确定了 VDR 基因多态性多个位点的单倍型频率。

结果

对于 VDR 基因 Alw I、Fok I、Apa I 和 Taq I 多态性,尿石症患者与健康对照组之间无统计学显著差异。钙结石患者与健康对照组之间也无统计学显著差异。在 13.5%的尿路结石患者和 8.3%的对照组中发现了一种新的单倍型(Ht 4;CTTT)(P=.001)。钙结石患者与对照组之间的单倍型频率差异有统计学意义(P=.004)。

结论

VDR 基因 Alw I、Fok I、Apa I 和 Taq I 多态性似乎不是韩国患者尿石症的候选遗传标记。然而,VDR 基因多态性多个位点的 1 个新单倍型可能是候选遗传标记。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验