首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Association of vitamin D receptor gene polymorphism (TaqI and Apa1) with bone mineral density in North Indian postmenopausal women
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Association of vitamin D receptor gene polymorphism (TaqI and Apa1) with bone mineral density in North Indian postmenopausal women

机译:维生素D受体基因多态性(Taqi和APA1)与北印度绝经后骨密度的骨密度

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Vitamin D receptor (VDR) gene has an important role as a candidate gene for the regulation of bone mass in osteoporosis. However, its association with bone mineral density (BMD) is controversial and has not been established in different ethnic populations. To enhance the understanding of VDR gene polymorphism in the context of BMD, we investigated the plausible genetic association of TaqI and ApaI polymorphism with BMD in North Indian postmenopausal women with osteoporosis.254 osteoporotic women (Age 55.82 +/- 6.91) and 254 postmenopausal non osteoporotic women (Age 54.76 +/- 6.26) were included in the study. VDR Taql and ApaI polymorphism were determined by PCR (polymerase chain reaction) and RFLP (restriction fragment length polymorphism). BMD was assessed by dual energy X-ray absorptiometry (DXA) at the lumbar spine (Lt-L4), hip, forearm and femoral neck. The average BMD with TT genotype was significantly lower at lumbar spine, hip and forearm. The Frequency of TT genotype and t allele was significantly high in osteoporotic women when compared with controls. The average BMD with Aa genotype was higher in ApaI. Furthermore, comparison of frequency distribution of genotype and allele for VDR Apal between osteoporotic patients and controls did not show any significant difference. Our findings revealed that Taql gene TT genotype was associated with low BMD in North Indian osteoporotic women. Moreover, TT genotype and t allele associated significantly with osteoporosis in postmenopausal women. Therefore, VDR Taql gene is an important determinant of risk factor for osteoporosis.
机译:维生素D受体(VDR)基因作为核糖基因的重要作用,用于调节骨质疏松症的骨质。然而,它与骨矿物密度(BMD)的关系是有争议的,并且尚未在不同的民族中建立。为了增强对BMD的背景下对VDR基因多态性的理解,我们调查了Taqi和Apai多态性的合理遗传学协会,与骨质疏松症的北印度绝经妇女BMD .254骨质疏松妇女(55.82 +/- 6.91)和254例绝经后血管非研究中纳入骨质疏松症妇女(54.76 +/- 6.26)。 VDR TaqL和Apai多态性由PCR(聚合酶链反应)和RFLP(限制性片段长度多态性)确定。 BMD通过腰椎(LT-L4),臀部,前臂和股骨颈的双能X射线吸收测定法(DXA)进行评估。腰椎,臀部和前臂具有TT基因型的平均BMD显着降低。与对照相比,骨质疏松症患者的TT基因型和T等位基因的频率显着高。 AA基因型的平均BMD在APAI中较高。此外,骨质疏松患者与对照组基因型和等位基因的频率分布的比较并没有显示出任何显着差异。我们的研究结果透露,Taql Gene TT基因型与北印度骨质疏松妇女的低BMD相关。此外,TT基因型和T等位基因显着与绝经后妇女骨质疏松症相关。因此,VDR TaqL基因是骨质疏松症的危险因素的重要决定因素。

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