首页> 外文OA文献 >Odnos polimorfizma gena za vitamin-D receptor, alfa-1 lanac kolagena I i estrogeni receptor i koštane mase u bolesnika s hipertireozom The association of polymorphisms of the vitamin-D receptor gene, collagen type I alpha-1 gene and estrogen receptor gene and bone mineral density in patients with hyperthyroidism
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Odnos polimorfizma gena za vitamin-D receptor, alfa-1 lanac kolagena I i estrogeni receptor i koštane mase u bolesnika s hipertireozom The association of polymorphisms of the vitamin-D receptor gene, collagen type I alpha-1 gene and estrogen receptor gene and bone mineral density in patients with hyperthyroidism

机译:Odnos polimorfizma gena za维生素D受体,alfa-1 lanac kolagena I i estrogeni receptorikoštanemaseu bolesnika s hipertireozom 维生素D受体基因多态性,I型胶原蛋白α-1基因和雌激素受体基因的关联性和甲状腺功能亢进症患者的骨密度

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摘要

Hyperthyroidism is a recognised risk factor for secondary osteoporosis. Little is known about the genetic origin of osteoporosis in patients with hyperthyroidism. This is the first study to examine the association between polymorphism of the VDR (TaqI), ERalpha (PvuII), COLIA1 (BalI) genes and BMD in premenopausal women with hyperthyroidism. This study comprised 45 premenopausal women, with the average age 40,4±7,7 years. The BMD was measured in using dual X-ray absorptiometry (DXA) in the L1-L4 region of the spine and femoral neck. Multivariate analysis found no significant correlation between polymorphisms of the 3 selected genes, individually or in combination, and BMD at the lumbar spine and femoral neck, and no correlation between polymorphisms and osteoporosis and osteopenia. A relationship was found between body mass index (BMI) and BMD at femoral neck in patients heterozygous for Taq1 polymorphism of the VDR gene and PvuII polymorphism of the ER gene, and homozygous for BalI polymorphism of the COL1AI. ----- CONCLUSION: A statistically significant association was not found between TaqI polymorphism of the VDR gene, PvuII polymorphism of the ERalpha gene and BalI polymorphism of the COLIA1 gene and BMD at the lumbar spine and femoral neck in hyperthyroid premenopausal women.
机译:甲状腺功能亢进是继发性骨质疏松症的公认危险因素。对于甲状腺功能亢进症患者的骨质疏松症的遗传起源知之甚少。这是首次研究绝经前甲状腺功能亢进妇女的VDR(TaqI),ERalpha(PvuII),COLIA1(BalI)基因多态性与BMD之间的相关性。这项研究包括45名绝经前妇女,平均年龄为40,4±7,7岁。使用双X线吸收法(DXA)在脊柱和股骨颈的L1-L4区域测量BMD。多变量分析发现,单个或组合的3个选定基因的多态性与腰椎和股骨颈的BMD之间无显着相关性,多态性与骨质疏松症和骨质减少症也无相关性。发现VDR基因Taq1多态性与ER基因PvuII多态性杂合和COL1AI BalI多态性纯合的患者股骨体重指数(BMI)与股骨颈BMD之间存在关联。 ---结论:在甲状腺功能绝经前妇女的腰椎和股骨颈VDR基因TaqI多态性,ERalpha基因PvuII多态性,ERIA基因BalI多态性和COLIA1基因BalI多态性与BMD之间没有统计学意义的关联。

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    Jelčić Jozo;

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  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 {"code":"hr","name":"Croatian","id":18}
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