Cai Hao, Sun Huan-Jian, Wang You-Hua, Zhang Zhe
Department of Orthopedics, Third People's Hospital of Yancheng, Xindu Road No.606, Yancheng, 224000, People's Republic of China,
Clin Rheumatol. 2015 Aug;34(8):1443-53. doi: 10.1007/s10067-014-2708-x. Epub 2014 Jun 21.
Observational and experimental studies have arrived at inconsistent conclusions about whether common polymorphisms in IL-6, IL-1A, and IL-1B genes are associated with an increased risk of osteoarthritis (OA). Therefore, we undertook a comprehensive meta-analysis to more systematically summarize the relationships of IL-6, IL-1A, and IL-1B genetic polymorphisms with susceptibility to OA. We screened the PubMed, Embase, Web of Science, Cochrane Library, CISCOM, CINAHL, Google Scholar, China BioMedicine (CBM), and China National Knowledge Infrastructure (CNKI) databases up to 31 March 2014. We used STATA software to analyze statistical data. Odds ratios (ORs) and their corresponding 95 % confidence intervals (95 % CIs) were calculated. Seventeen independent case-control studies were included in this meta-analysis with a total number of 7,491 subjects, comprised of 3,293 OA patients and 4,729 healthy controls. Our results indicate that IL-6, IL-1A, and IL-1B genetic polymorphisms are statistically correlated with an increased risk of OA under the allele and dominant models. According to a subgroup analysis based on disease, a higher frequency of IL-6 genetic polymorphisms was observed among knee OA and hand OA patients, but not among hip OA and DIP OA patients. A higher frequency of IL-1A genetic polymorphisms were found among hip OA patients, hand OA, hip OA and DIP OA patients. Furthermore, we observed a higher IL-1B polymorphism frequency among knee OA and hip OA patients, but not among hand OA patients. Our findings provide evidence that IL-6, IL-1A, and IL-1B genetic polymorphisms may be correlated with susceptibility to OA.
关于白细胞介素6(IL-6)、白细胞介素1A(IL-1A)和白细胞介素1B(IL-1B)基因的常见多态性是否与骨关节炎(OA)风险增加相关,观察性研究和实验性研究得出了不一致的结论。因此,我们进行了一项全面的荟萃分析,以便更系统地总结IL-6、IL-1A和IL-1B基因多态性与OA易感性之间的关系。我们检索了截至2014年3月31日的PubMed、Embase、科学网、考克兰图书馆、CISCOM、护理学与健康领域数据库(CINAHL)、谷歌学术、中国生物医学文献数据库(CBM)和中国知网数据库。我们使用STATA软件分析统计数据。计算比值比(OR)及其相应的95%置信区间(95%CI)。本荟萃分析纳入了17项独立的病例对照研究,共有7491名受试者,其中包括3293例OA患者和4729名健康对照。我们的结果表明,在等位基因模型和显性模型下,IL-6、IL-1A和IL-1B基因多态性与OA风险增加在统计学上相关。根据基于疾病的亚组分析,在膝关节OA和手部OA患者中观察到IL-6基因多态性的频率较高,但在髋关节OA和远端指间关节(DIP)OA患者中未观察到。在髋关节OA患者、手部OA、髋关节OA和DIP OA患者中发现IL-1A基因多态性的频率较高。此外,我们在膝关节OA和髋关节OA患者中观察到较高的IL-1B多态性频率,但在手部OA患者中未观察到。我们的研究结果提供了证据,表明IL-6、IL-1A和IL-1B基因多态性可能与OA易感性相关。