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Association between seven common OPG genetic polymorphisms and osteoporosis risk: a meta-analysis.

机译:七种常见OPG基因多态性与骨质疏松症风险之间的关联:一项荟萃分析。

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Functional polymorphisms of the osteoprotegerin (OPG) gene are known to be involved in bone mineral density and the development of osteoporosis; however, some conflicting results have been reported. The aim of this meta-analysis is to provide a relatively comprehensive assessment of the relationship between seven common OPG genetic polymorphisms (T149C, A163G, G209A, T245G, T950C, G1181C, and C1217T) and osteoporosis risk. A literature search for eligible studies published before August 1st, 2013 was conducted in PubMed, Embase, Web of Science, Cochrane Library, and CNKI (China National Knowledge Infrastructure) databases. Pooled odds ratios and their corresponding 95% confidence intervals were used to evaluate the strength of the association under fixed- or random-effect models according to a heterogeneity test. All analyses were performed using the STATA software, version 12.0. Fourteen case-control studies with a total of 2383 osteoporosis cases and 2280 healthy controls were included in this meta-analysis. Among the seven polymorphisms, A163G and G1181C revealed significant associations with osteoporosis risk. For A163G (rs3102735), the combined results showed that the G allele of the A163G polymorphism may be associated with an increased risk of osteoporosis. Stratified analyses showed that the magnitude of the effect was similar in Caucasian and postmenopausal woman subgroups. For G1181C (rs2073618), however, we found that individuals with the C allele of the G1181C polymorphism had a decreased risk of osteoporosis, especially in Asian and postmenopausal woman subgroups. In summary, this meta-analysis indicated that the G allele of the OPG A163G polymorphism might increase osteoporosis risk in Caucasians, whereas individuals with the C allele of the G1181C polymorphism had a decreased risk of osteoporosis, especially in Asians. Both of these effects were observed in postmenopausal women. These polymorphisms could probably be used with other genetic markers together to identify individuals at a high risk of osteoporosis.Registry Number/Name of Substance 0 (Osteoprotegerin).
机译:众所周知,骨保护素(OPG)基因的功能多态性与骨矿物质密度和骨质疏松症的发生有关。但是,据报道有些矛盾的结果。这项荟萃分析的目的是对七个常见的OPG遗传多态性(T149C,A163G,G209A,T245G,T950C,G1181C和C1217T)与骨质疏松症风险之间的关系进行相对全面的评估。在PubMed,Embase,Web of Science,Cochrane图书馆和CNKI(中国国家知识基础设施)数据库中对2013年8月1日之前发表的合格研究进行了文献检索。根据异质性检验,使用合并的优势比及其相应的95%置信区间来评估固定或随机效应模型下的关联强度。所有分析均使用STATA软件12.0版进行。这项荟萃分析包括14例病例对照研究,总计2383例骨质疏松症病例和2280例健康对照。在这七个多态性中,A163G和G1181C显示出与骨质疏松症风险显着相关。对于A163G(rs3102735),综合结果显示,A163G多态性的G等位基因可能与骨质疏松症的风险增加有关。分层分析显示,这种影响的程度在白人和绝经后的女性亚组中相似。但是,对于G1181C(rs2073618),我们发现具有G1181C多态性C等位基因的个体患骨质疏松症的风险降低,尤其是在亚洲和绝经后的女性亚组中。总之,这项荟萃分析表明,OPG A163G多态性的G等位基因可能会增加白种人的骨质疏松症风险,而具有G1181C多态性的C等位基因的人则骨质疏松症的风险降低,尤其是在亚洲人中。在绝经后妇女中都观察到了这两种作用。这些多态性可能可以与其他遗传标记一起使用,以鉴定骨质疏松症高危人群。注册号/物质0的名称(Osteoprotegerin)。

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