Suppr超能文献

ESR1 和 ESR2 多态性与骨质疏松症风险的关联:一项更新的荟萃分析。

Association between the ESR1 and ESR2 polymorphisms and osteoporosis risk: An updated meta-analysis.

机构信息

Heping Hospital Affiliated to Changzhi Medical College, Changzhi, Shanxi, China.

Department of Biochemistry, Changzhi Medical College, Changzhi, China.

出版信息

Medicine (Baltimore). 2023 Oct 13;102(41):e35461. doi: 10.1097/MD.0000000000035461.

Abstract

BACKGROUND

Gene polymorphisms of estrogen receptor (ESR) 1 PvuII (rs2234693), XbaI (rs9340799), G2014A (rs2228480), ESR2 AluI (rs4986938), and RsaI (rs1256049) had been reported to be associated with the risk of osteoporosis. However, these conclusions were inconsistent, therefore, an updated meta-analysis was conducted to further explore these issues.

OBJECTIVE

To evaluate the association between gene polymorphisms of ESR1 PvuII (rs2234693), XbaI (rs9340799), G2014A (rs2228480), ESR2 AluI (rs4986938), RsaI (rs1256049), and osteoporosis risk.

MATERIALS AND METHODS

PubMed, Medline, Ovid, Embase, CNKI, and China Wanfang databases were searched. Association was assessed using odds ratio with 95% confidence interval. Moreover, the false-positive reporting probability, Bayesian false-finding probability, and Venetian criteria were used to assess the credibility of statistically significant associations.

RESULTS

Overall, ESR1 PvuII (rs2234693) and XbaI (rs9340799) were associated with the risk of osteoporosis in Indians. Moreover, ESR1 G2014A (rs2228480) was associated with the decreased risk of osteoporosis in East Asians. Moreover, ESR2 Alul (rs4986938) was associated with the increased risk of osteoporosis in East Asians and Caucasians. There was a significant association between ESR2 Rsal (rs1256049) and osteoporosis risk in overall population. When only high-quality and Hardy-Weinberg equilibrium studies were included in the sensitivity analysis, all results did not change in the present study. When the credibility was evaluated applying false-positive reporting probability, Bayesian false-finding probability, and Venetian criteria, all significant associations were considered as false positive results.

CONCLUSIONS

In summary, this study shows that all substantial associations between gene polymorphisms of ESR1 (PvuII, XbaI, and G2014A) and ESR 2 (AluI and RsaI) and osteoporosis risk are possibly false positive results instead of real associations or biological variables.

摘要

背景

雌激素受体(ESR)1 PvuII(rs2234693)、XbaI(rs9340799)、G2014A(rs2228480)、ESR2 AluI(rs4986938)和 RsaI(rs1256049)的基因多态性与骨质疏松症的风险有关。然而,这些结论并不一致,因此,进行了一项更新的荟萃分析以进一步探讨这些问题。

目的

评估 ESR1 PvuII(rs2234693)、XbaI(rs9340799)、G2014A(rs2228480)、ESR2 AluI(rs4986938)、RsaI(rs1256049)基因多态性与骨质疏松症风险之间的关联。

材料和方法

检索 PubMed、Medline、Ovid、Embase、CNKI 和中国万方数据库。使用优势比和 95%置信区间评估相关性。此外,还使用虚假阳性报告概率、贝叶斯假发现概率和威尼斯标准来评估统计学显著关联的可信度。

结果

总体而言,ESR1 PvuII(rs2234693)和 XbaI(rs9340799)与印度人骨质疏松症的风险相关。此外,ESR1 G2014A(rs2228480)与东亚人骨质疏松症风险降低相关。此外,ESR2 AluI(rs4986938)与东亚人和高加索人骨质疏松症风险增加相关。ESR2 Rsal(rs1256049)与总体人群骨质疏松症风险之间存在显著关联。当仅包括高质量和 Hardy-Weinberg 平衡研究的敏感性分析时,本研究中的所有结果均未发生变化。当应用虚假阳性报告概率、贝叶斯假发现概率和威尼斯标准评估可信度时,所有显著关联均被认为是假阳性结果。

结论

总之,本研究表明,ESR1(PvuII、XbaI 和 G2014A)和 ESR2(AluI 和 RsaI)基因多态性与骨质疏松症风险之间的所有实质性关联可能都是假阳性结果,而不是真实关联或生物学变量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d5f/10578747/ffd99ec3cf66/medi-102-e35461-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验