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首页> 外文期刊>Clinical rheumatology >Relationships of common polymorphisms in IL-6, IL-1A, and IL-1B genes with susceptibility to osteoarthritis: a meta-analysis
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Relationships of common polymorphisms in IL-6, IL-1A, and IL-1B genes with susceptibility to osteoarthritis: a meta-analysis

机译:IL-6,IL-1A和IL-1B基因常见多态性与骨关节炎易感性的荟萃分析

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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.
机译:关于IL-6,IL-1A和IL-1B基因的常见多态性是否与骨关节炎(OA)风险增加相关,观察性和实验性研究得出的结论不一致。因此,我们进行了全面的荟萃分析,以更系统地总结IL-6,IL-1A和IL-1B遗传多态性与OA易感性的关系。我们筛选了截至2014年3月31日的PubMed,Embase,Web of Science,Cochrane图书馆,CISCOM,CINAHL,Google Scholar,中国生物医学(CBM)和中国国家知识基础设施(CNKI)数据库。我们使用STATA软件分析统计数据。 。计算出赔率(OR)及其对应的95%置信区间(95%CI)。该荟萃分析包括十七项独立的病例对照研究,总数为7,491名受试者,包括3,293名OA患者和4,729名健康对照。我们的结果表明,在等位基因和显性模型下,IL-6,IL-1A和IL-1B的遗传多态性与OA风险增加在统计学上相关。根据疾病进行的亚组分析,在膝骨OA和手部OA患者中观察到较高的IL-6基因多态性,而髋部OA和DIP OA患者中未观察到。在髋骨OA患者,手骨OA,髋骨OA和DIP OA患者中,IL-1A基因多态性的发生率较高。此外,我们观察到膝OA和髋OA患者中IL-1B多态性频率更高,而手OA患者则不然。我们的发现提供了IL-6,IL-1A和IL-1B遗传多态性可能与OA易感性相关的证据。

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