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骨保护素基因多态性与中国绝经后妇女骨质疏松症的关系。

Association between osteoprotegerin genetic variants and osteoporosis in Chinese postmenopausal women.

机构信息

Department of Orthopaedic Surgery, No. 98 Hospital of PLA, Huzhou 313000, People's Republic of China.

出版信息

Endocr J. 2013;60(12):1303-7. doi: 10.1507/endocrj.ej13-0308. Epub 2013 Sep 25.

DOI:10.1507/endocrj.ej13-0308
PMID:24067544
Abstract

The objective of this study was to evaluate the association of single nucleotide polymorphisms (SNPs) of osteoprotegerin gene (OPG) with bone mineral density (BMD) and osteoporosis. A total of 338 Chinese postmenopausal women with primary osteoporosis and 367 healthy controls were enrolled. The lumbar spine (L₂₋₄), total hip and femoral neck hip of BMD were assessed by dual-energy X-ray absorptiometry (DEXA). OPG genetic variants were genotyped through polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), created restriction site-PCR (CRS-PCR) and DNA sequencing methods. In this study, the g.18861A>G and g.25548C>T SNPs were detected and our data suggested that the significant differences of spine BMD, femoral neck hip BMD and total hip BMD were found among different g.18861A>G genotype, subjects with the AA genotype were significantly higher than those of AG and GG genotypes (p < 0.05). The g.25548C>T variant was not significantly associated with spine BMD, femoral neck hip BMD and total hip BMD (p > 0.05), while almost reached at the significant level in total hip BMD (p = 0.061). These findings suggeste that OPG gene variants are related to BMD and osteoporosis in Chinese postmenopausal women.

摘要

本研究旨在评估骨保护素基因(OPG)单核苷酸多态性(SNPs)与骨密度(BMD)和骨质疏松症的相关性。共纳入 338 例原发性骨质疏松症的绝经后中国女性和 367 名健康对照者。采用双能 X 线吸收法(DEXA)评估腰椎(L₂₋₄)、全髋和股骨颈骨密度。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)、创建限制性位点-PCR(CRS-PCR)和 DNA 测序方法对 OPG 遗传变异进行基因分型。在本研究中,检测到 g.18861A>G 和 g.25548C>T SNP,我们的数据表明,不同 g.18861A>G 基因型之间的脊柱 BMD、股骨颈 BMD 和全髋 BMD 存在显著差异,AA 基因型的受试者明显高于 AG 和 GG 基因型(p < 0.05)。g.25548C>T 变体与脊柱 BMD、股骨颈 BMD 和全髋 BMD 无显著相关性(p > 0.05),而在全髋 BMD 中几乎达到显著水平(p = 0.061)。这些发现提示 OPG 基因变异与中国绝经后妇女的 BMD 和骨质疏松症有关。

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引用本文的文献

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Association between polymorphisms and osteoporosis risk: An updated meta-analysis.基因多态性与骨质疏松症风险之间的关联:一项更新的荟萃分析。
Front Genet. 2022 Nov 9;13:1032110. doi: 10.3389/fgene.2022.1032110. eCollection 2022.
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Association between osteoprotegerin gene T950C polymorphism and osteoporosis risk in the Chinese population: Evidence via meta-analysis.骨保护素基因T950C多态性与中国人群骨质疏松症风险的关联:Meta分析证据
PLoS One. 2017 Dec 18;12(12):e0189825. doi: 10.1371/journal.pone.0189825. eCollection 2017.
3
Association analysis between g.18873C>T and g.27522G>A genetic polymorphisms of OPG and bone mineral density in Chinese postmenopausal women.
中国绝经后女性中骨保护素基因g.18873C>T和g.27522G>A多态性与骨密度的关联分析
Biomed Res Int. 2014;2014:320828. doi: 10.1155/2014/320828. Epub 2014 Dec 15.