Suppr超能文献

土耳其人群中维生素D受体基因多态性与骨质疏松症

Vitamin D receptor gene polymorphism and osteoporosis in the Turkish population.

作者信息

Uysal Ali Riza, Sahin Mustafa, Gürsoy Alptekin, Güllü Sevim

机构信息

Department of Endocrinology and Metabolic Diseases, Ankara University School of Medicine, Ibni Sina Hospital, Ankara, Turkey.

出版信息

Genet Test. 2008 Dec;12(4):591-4. doi: 10.1089/gte.2008.0052.

Abstract

Osteoporosis is one of the most important medical problems facing the aging population. It is defined as a decrease in the bone mass leading to an unacceptably high risk of fractures. Osteoporosis is a multifactorial disease. It is well established that genetic factors are involved in the pathogenesis of osteoporosis. Polymorphism of the vitamin D receptor (VDR) gene has been reported to play a major role in variations for genetic regulation of bone mass. Its role within various ethnic populations is not clear. The purpose of this project was to determine the frequencies of VDR genotypes in Turkey. Three polymorphisms of the VDR gene were analyzed using the polymerase chain reaction-restriction fragment length polymorphism technique. The sample for our study was comprised of postmenopausal women in Turkey, 100 of whom were diagnosed with osteoporosis. They were compared with 146 healthy controls. BsmI genotype frequencies in Turks resemble Caucasians rather than Asians, and Taq genotype frequencies in Turks neither resemble Caucasians nor Asians. The genotype frequencies of VDR were not statistically different between patients with osteoporosis and the control group. Among VDR haplotypes, bbAATT and bbTtAa are more frequent in the osteoporosis group than the control group.

摘要

骨质疏松症是老龄人口面临的最重要的医学问题之一。它被定义为骨量减少,导致骨折风险高到不可接受的程度。骨质疏松症是一种多因素疾病。众所周知,遗传因素参与骨质疏松症的发病机制。据报道,维生素D受体(VDR)基因多态性在骨量遗传调控变异中起主要作用。其在不同种族人群中的作用尚不清楚。本项目的目的是确定土耳其VDR基因型的频率。使用聚合酶链反应-限制性片段长度多态性技术分析VDR基因的三种多态性。我们研究的样本包括土耳其绝经后妇女,其中100人被诊断为骨质疏松症。将她们与146名健康对照进行比较。土耳其人的BsmI基因型频率与高加索人相似,而非亚洲人,土耳其人的Taq基因型频率既不与高加索人相似,也不与亚洲人相似。骨质疏松症患者与对照组之间VDR的基因型频率无统计学差异。在VDR单倍型中,bbAATT和bbTtAa在骨质疏松症组中比对照组更常见。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验