首页> 美国卫生研究院文献>Pakistan Journal of Medical Sciences >The polymorphism of Insulin-like growth factor-I (IGF-I) is related to osteoporosis and bone mineral density in postmenopausal population
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The polymorphism of Insulin-like growth factor-I (IGF-I) is related to osteoporosis and bone mineral density in postmenopausal population

机译:胰岛素样生长因子-I(IGF-I)的多态性与绝经后人群的骨质疏松症和骨矿物质密度有关

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摘要

>Objective: It has been shown that Insulin-like growth factor-1 (IGF-1) may be related with bone mineral density (BMD) or osteoporosis. But there are few evidences on the role of genetic variation of IGF-1 on the BMD or osteoporosis. We observed the relationship between polymorphisms of IGF-1(rs35767, rs2288377 and rs5742612) with osteoporosis and BMD in the postmenopausal female population in our study. >Methods: A total of 216 postmenopausal women with a primary diagnosis of osteoporosis and 220 normal healthy women were included in the study. Genomic DNA of IGF-1 rs35767, rs2288377 and rs5742612 was extracted from the whole blood using QIAamp blood DNA mini kits (QIAGEN, Hilden, Germany) according to the methods recommended by the manufacturer. >Results: We found that T allele of rs35767 had higher increased risk of osteoporosis (OR=1.34, 95%CI=1.0-1.81). Those carrying T allele of rs35767 had a significant lower BMD at L1–L4 vertebrae, femoral neck, total hip and trochanter when compared with those carrying C allele (P < 0.05). In addition, the BMD of L1–L4 vertebrae, femoral neck, total hip and trochanter decreased by 2.09%, 3.74%, 3.52% and 2.54% in women carrying T alleles compared with those carrying C alleles. >Conclusion: Our study suggests that polymorphism in IGF-I rs35767 was significantly associated with BMD and osteoporosis in postmenopausal female population, and polymorphism of rs35767 could be a marker for lower BMD and risk of osteoporosis.
机译:>目的:已经表明,胰岛素样生长因子-1(IGF-1)可能与骨密度(BMD)或骨质疏松症有关。但是,关于IGF-1基因变异对BMD或骨质疏松的作用的证据很少。在我们的研究中,我们观察到了IGF-1多态性(rs35767,rs2288377和rs5742612)与骨质疏松症和BMD的关系。 >方法:该研究共纳入了216名主要诊断为骨质疏松的绝经后妇女和220名正常健康妇女。根据制造商推荐的方法,使用QIAamp血液DNA微型试剂盒(QIAGEN,Hilden,德国)从全血中提取IGF-1 rs35767,rs2288377和rs5742612的基因组DNA。 >结果:我们发现rs35767的T等位基因具有更高的骨质疏松症风险(OR = 1.34,95%CI = 1.0-1.81)。与携带C等位基因的人相比,携带rs35767 T等位基因的人在L1–L4椎骨,股骨颈,全髋关节和转子上的BMD显着降低(P <0.05)。此外,与携带C等位基因的女性相比,携带T等位基因的女性的L1-L4椎骨,股骨颈,全髋关节和转子的骨密度降低了2.09%,3.74%,3.52%和2.54%。 >结论:我们的研究表明,绝经后女性人群中IGF-I rs35767的多态性与BMD和骨质疏松症密切相关,而rs35767的多态性可能是降低BMD和骨质疏松症风险的标志。

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