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血管紧张素转换酶插入/缺失多态性与膝关节骨关节炎易感性:一项病例对照研究与荟萃分析

Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism and Susceptibility to Osteoarthritis of the Knee: A Case-Control Study and Meta-Analysis.

作者信息

Lin Chin, Chen Hsiang-Cheng, Fang Wen-Hui, Wang Chih-Chien, Peng Yi-Jen, Lee Herng-Sheng, Chang Hung, Chu Chi-Ming, Huang Guo-Shu, Chen Wei-Teing, Tsai Yu-Jui, Lin Hong-Ling, Lin Fu-Huang, Su Sui-Lung

机构信息

School of Public Health, National Defense Medical Center, Taipei, Taiwan, ROC.

Division of Rheumatology/Immunology/Allergy, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC.

出版信息

PLoS One. 2016 Sep 22;11(9):e0161754. doi: 10.1371/journal.pone.0161754. eCollection 2016.

Abstract

BACKGROUND

Studies of angiotensin-converting enzyme insertion/deletion (ACE I/D) polymorphisms and the risks of knee osteoarthritis (OA) have yielded conflicting results.

OBJECTIVE

To determine the association between ACE I/D and knee OA, we conducted a combined case-control study and meta-analysis.

METHODS

For the case-control study, 447 knee OA cases and 423 healthy controls were recruited between March 2010 and July 2011. Knee OA cases were defined using the Kellgren-Lawrence grading system, and the ACE I/D genotype was determined using a standard polymerase chain reaction. The association between ACE I/D and knee OA was detected using allele, genotype, dominant, and recessive models. For the meta-analysis, PubMed and Embase databases were systematically searched for prospective observational studies published up until August 2015. Studies of ACE I/D and knee OA with sufficient data were selected. Pooled results were expressed as odds ratios (ORs) with corresponding 95% confidence intervals (CI) for the D versus I allele with regard to knee OA risk.

RESULTS

We found no significant association between the D allele and knee OA [OR: 1.09 (95% CI: 0.76-1.89)] in the present case-control study, and the results of other genetic models were also nonsignificant. Five current studies were included, and there were a total of six study populations after including our case-control study (1165 cases and 1029 controls). In the meta-analysis, the allele model also yielded nonsignificant results [OR: 1.37 (95% CI: 0.95-1.99)] and a high heterogeneity (I2: 87.2%).

CONCLUSIONS

The association between ACE I/D and knee OA tended to yield negative results. High heterogeneity suggests a complex, multifactorial mechanism, and an epistasis analysis of ACE I/D and knee OA should therefore be conducted.

摘要

背景

血管紧张素转换酶插入/缺失(ACE I/D)多态性与膝关节骨关节炎(OA)风险的研究结果相互矛盾。

目的

为确定ACE I/D与膝关节OA之间的关联,我们进行了一项病例对照联合研究及荟萃分析。

方法

在病例对照研究中,于2010年3月至2011年7月招募了447例膝关节OA患者和423例健康对照。膝关节OA患者采用Kellgren-Lawrence分级系统进行定义,ACE I/D基因型通过标准聚合酶链反应确定。采用等位基因、基因型、显性和隐性模型检测ACE I/D与膝关节OA之间的关联。在荟萃分析中,系统检索了PubMed和Embase数据库中截至2015年8月发表的前瞻性观察性研究。选择了具有足够数据的ACE I/D与膝关节OA的研究。汇总结果以优势比(OR)及相应的95%置信区间(CI)表示,用于比较D等位基因与I等位基因在膝关节OA风险方面的差异。

结果

在本病例对照研究中,我们发现D等位基因与膝关节OA之间无显著关联[OR:1.09(95%CI:0.76 - 1.89)],其他遗传模型的结果也无统计学意义。纳入了五项现有研究,纳入我们的病例对照研究后共有六个研究群体(1165例病例和1029例对照)。在荟萃分析中,等位基因模型也得出无统计学意义的结果[OR:1.37(95%CI:0.95 - 1.99)],且异质性较高(I²:87.2%)。

结论

ACE I/D与膝关节OA之间的关联倾向于得出阴性结果。高异质性提示存在复杂的多因素机制,因此应进行ACE I/D与膝关节OA的上位性分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9740/5033346/4a9ba379bfd0/pone.0161754.g001.jpg

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