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绝经后印度女性的维生素D受体基因多态性与骨密度

Vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Indian women.

作者信息

Mitra Sumegha, Desai Meena, Ikram Khatkhatay M

机构信息

Molecular Immuno-diagnostics Division, National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai 400012, India.

出版信息

Maturitas. 2006 Aug 20;55(1):27-35. doi: 10.1016/j.maturitas.2006.01.003. Epub 2006 Feb 7.

Abstract

OBJECTIVES

Osteoporosis is a common condition in postmenopausal women. Bone mineral density (BMD), the major determinant of osteoporotic fracture risk, has a particular genetic background. However, consensus on the association of BMD with specific gene locus has not been reached. The race and ethnicity specific divergence in association studies must be assessed to predict the susceptibility and therapeutic response of associated genes. We investigated the potential association of Vitamin D receptor (VDR) gene polymorphisms ApaI, BsmI, FokI and TaqI with BMD in 246 postmenopausal Indian women (average age 54.2+/-3.4 years).

METHODS

The subjects were genotyped by PCR-RFLP and underwent BMD measurements at spine and hip by dual energy X-ray absorptiometery.

RESULTS

The average BMD at spine and hip of women with genotypes aa, bb (presence of restriction sites for ApaI and BsmI), FF and TT (absence of restriction sites for FokI and TaqI) was more than 10% higher than those with genotypes AA, BB, ff and tt, respectively. The interaction between BsmI, ApaI and TaqI genotypes showed significant effect of BsmI-ApaI genotypes (p=0.052) in this combination on BMD. However, presence of T allele in combination showed positive influence on BMD. Within the group, genotypes BB, ff and tt were significantly prevalent in women with osteoporotic bone mass, tt and BB had significantly higher adjusted odd ratio (OR) for age more than 55years.

CONCLUSION

Study reveals that VDR gene polymorphisms are associated with BMD in Indian women and perhaps, influence some determinant of bone metabolism. Ethnicity may attribute to frequency variation, however, allele impact remains same.

摘要

目的

骨质疏松症是绝经后女性的常见病症。骨矿物质密度(BMD)是骨质疏松性骨折风险的主要决定因素,具有特定的遗传背景。然而,关于BMD与特定基因位点的关联尚未达成共识。必须评估关联研究中种族和民族的特异性差异,以预测相关基因的易感性和治疗反应。我们调查了246名绝经后印度女性(平均年龄54.2±3.4岁)中维生素D受体(VDR)基因多态性ApaI、BsmI、FokI和TaqI与BMD之间的潜在关联。

方法

通过PCR-RFLP对受试者进行基因分型,并采用双能X线吸收法测量脊柱和髋部的BMD。

结果

基因型为aa、bb(存在ApaI和BsmI的限制性位点)、FF和TT(不存在FokI和TaqI的限制性位点)的女性,其脊柱和髋部的平均BMD分别比基因型为AA、BB、ff和tt的女性高出10%以上。BsmI、ApaI和TaqI基因型之间的相互作用显示,这种组合中的BsmI-ApaI基因型对BMD有显著影响(p = 0.052)。然而,T等位基因的组合对BMD有积极影响。在该组中,基因型BB、ff和tt在骨质疏松骨量的女性中显著普遍,tt和BB在年龄超过55岁的女性中调整后的优势比(OR)显著更高。

结论

研究表明,VDR基因多态性与印度女性的BMD相关,可能影响骨代谢的某些决定因素。种族可能导致频率差异,然而,等位基因的影响保持不变。

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