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首页> 外文期刊>Journal of bone and mineral metabolism >Lack of association between the HindIII RFLP of the osteocalcin (BGP) gene and bone mineral density (BMD) in healthy pre- and postmenopausal Chinese women.
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Lack of association between the HindIII RFLP of the osteocalcin (BGP) gene and bone mineral density (BMD) in healthy pre- and postmenopausal Chinese women.

机译:在健康的绝经前和绝经后的中国女性中,骨钙素(BGP)基因的HindIII RFLP与骨矿物质密度(BMD)之间缺乏关联。

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摘要

In Caucasian populations, the polymorphic restriction endonuclease HindIII marker of the osteocalcin (also known as BGP, for bone Gla protein) gene has recently been reported to be associated with bone mass, a major risk determinant of osteoporosis. In this study, we investigated the relationship between the BGP HindIII polymorphism and bone mineral density (BMD) in 388 premenopausal (31.18 +/- 5.92 years) and 169 postmenopausal (58.90 +/- 6.27 years) Chinese women. The BMD of spine and hip was measured by dual-energy X-ray absorptiometry (DEXA). All the study subjects were genotyped at the HindIII site of the BGP gene by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) detecting methods. The BGP alleles were designated according to the absence ( H) or presence ( h) of the HindIII restriction site. We did not find any significant difference in spine and hip BMD across BGP genotypes in either pre- or postmenopausal women or the combined group. Our result is not consistent with recent reports that the HindIII marker of the BGP gene is associated with osteoporosis. The different findings may reflect inter-population differences in the association (i.e., linkage disequilibrium) of molecular markers with BMD, and indicate the limit of using the HindIII marker of the BGP gene as a genetic marker to discern women susceptible to low BMD and thus osteoporosis in Chinese.
机译:在高加索人群中,骨钙蛋白(也称为BGP,用于骨Gla蛋白)基因的多态性限制性核酸内切酶HindIII标记物最近有报道与骨量有关,骨量是骨质疏松症的主要危险因素。在这项研究中,我们调查了中国绝经前388名(31.18 +/- 5.92岁)和绝经后169名(58.90 +/- 6.27岁)的BGP HindIII多态性与骨矿物质密度(BMD)的关系。脊柱和髋部的BMD通过双能X射线吸收法(DEXA)测量。所有研究对象均通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测方法在BGP基因的HindIII位点进行基因分型。 BGP等位基因根据HindIII限制性位点的不存在(H)或存在(h)来指定。在绝经前或绝经后妇女或合并组中,我们没有发现BGP基因型在脊柱和髋部BMD上有任何显着差异。我们的结果与BGP基因的HindIII标志物与骨质疏松症相关的最新报道不一致。不同的发现可能反映了群体间分子标记物与BMD的关联性(即连锁不平衡)的差异,并表明使用BGP基因的HindIII标记物作为遗传标记物来识别易患低BMD的女性的局限性,因此骨质疏松症。

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