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SMAD3基因rs12901499多态性与骨关节炎风险的关联:一项荟萃分析。

The association between rs12901499 polymorphism in SMAD3 gene and risk of osteoarthritis: a meta-analysis.

作者信息

Gao Shu-Tao, Lv Zheng-Tao, Sheng Wei-Bin

机构信息

Department of Spine Surgery, The First Affiliate Hospital, Xinjiang Medical University, Urumqi, Xinjiang, China.

Department of Orthopedics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

出版信息

Ther Clin Risk Manag. 2018 May 15;14:929-936. doi: 10.2147/TCRM.S164409. eCollection 2018.

Abstract

PURPOSE

This study was conducted to assess and synthesize the current evidence on the association between rs12901499 polymorphism in SMAD3 gene and risk of osteoarthritis (OA).

MATERIALS AND METHODS

Four electronic databases, including PubMed, Embase, ISI Web of Science, and CENTRAL were systematically searched for potential studies. Summary odds ratio and corresponding 95% CI were calculated to evaluate the association. Risk of bias was assessed through the Newcastle-Ottawa Scale. Subgroups and sensitivity analyses were performed using the RevMan 5.3 software. Publication bias was evaluated by Egger's and Begg's tests. Power analysis was conducted using the Power and Sample Size Calculation program.

RESULTS

Eight case-control studies containing 5,625 patients with OA and 5,600 healthy controls were obtained for the meta-analysis. After excluding cohorts with inadequate power, the pooled data supported that G allele carriers of rs12901499 had a significantly increased risk of OA (odds ratio 1.31, 95% CI: 1.21 to 1.43, <0.00001). When stratified by OA site and ethnicity, the association remained statistically significant.

CONCLUSION

The combined results evidently supported that rs12901499 polymorphism in SMAD3 gene is significantly associated with OA vulnerability across both Caucasian and Asian populations.

摘要

目的

本研究旨在评估和综合目前关于SMAD3基因中rs12901499多态性与骨关节炎(OA)风险之间关联的证据。

材料与方法

系统检索了四个电子数据库,包括PubMed、Embase、ISI Web of Science和CENTRAL,以查找潜在的研究。计算汇总比值比及相应的95%置信区间来评估这种关联。通过纽卡斯尔-渥太华量表评估偏倚风险。使用RevMan 5.3软件进行亚组分析和敏感性分析。通过Egger检验和Begg检验评估发表偏倚。使用功效和样本量计算程序进行功效分析。

结果

共纳入八项病例对照研究,包括5625例骨关节炎患者和5600例健康对照进行荟萃分析。在排除功效不足的队列后,汇总数据支持rs12901499的G等位基因携带者患骨关节炎的风险显著增加(比值比1.31,95%置信区间:1.21至1.43,<0.00001)。按骨关节炎部位和种族分层时,这种关联仍具有统计学意义。

结论

综合结果明显支持,SMAD3基因中的rs12901499多态性与白种人和亚洲人群患骨关节炎的易感性显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e79c/5960251/a10823fe2c54/tcrm-14-929Fig1.jpg

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