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首页> 外文期刊>Journal of Osteoporosis >Lack of Association of Bone Morphogenetic Protein 2 Gene Haplotypes with Bone Mineral Density, Bone Loss, or Risk of Fractures in Men
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Lack of Association of Bone Morphogenetic Protein 2 Gene Haplotypes with Bone Mineral Density, Bone Loss, or Risk of Fractures in Men

机译:缺乏骨形态发生蛋白2基因单倍型与骨密度,骨丢失或男性骨折的风险。

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Introduction. The association of bone morphogenetic protein 2 (BMP2) with BMD and risk of fracture was suggested by a recent linkage study, but subsequent studies have been contradictory. We report the results of a study of the relationship between BMP2 genotypes and BMD, annual change in BMD, and risk of fracture in male subjects.Materials and Methods. We tested three single-nucleotide polymorphisms (SNPs) across the BMP2 gene, including Ser37Ala SNP, in 342 Caucasian Englishmen, comprising 224 control and 118 osteoporotic subjects.Results. BMP2 SNP1 (Ser37Ala) genotypes were found to have similar low frequency in control subjects and men with osteoporosis. The major informative polymorphism, BMP2 SNP3 (Arg190Ser), showed no statistically significant association with weight, height, BMD, change in BMD at hip or lumbar spine, and risk of fracture.Conclusion. There were no genotypic or haplotypic effects of the BMP2 candidate gene on BMD, change in BMD, or fracture risk identified in this cohort.
机译:介绍。最近的一项连锁研究提示骨形态发生蛋白2(BMP2)与BMD和骨折风险之间的关系,但随后的研究却相互矛盾。我们报告了一项关于BMP2基因型与BMD,BMD年度变化以及男性受试者骨折风险之间关系的研究结果。材料和方法。我们在342名白人英国人中测试了BMP2基因的三个单核苷酸多态性(SNP),包括Ser37Ala SNP,包括224名对照者和118名骨质疏松症患者。发现BMP2 SNP1(Ser37Ala)基因型在对照组和骨质疏松症患者中具有相似的低频率。主要的信息多态性BMP2 SNP3(Arg190Ser)与体重,身高,BMD,髋部或腰椎BMD的变化以及骨折风险没有统计学意义的关联。在此队列中,没有发现BMP2候选基因对BMD,BMD变化或骨折风险有基因型或单倍型作用。

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