Department of Biomathematics, University of Thessaly School of Medicine, 2 Panepistimiou Street, Biopolis, Larissa 41110, Greece.
Am J Epidemiol. 2010 Apr 15;171(8):851-8. doi: 10.1093/aje/kwq016. Epub 2010 Mar 17.
A comprehensive and systematic assessment of the current status of genetic association studies (GAS) for osteoarthritis was conducted. Data from 327 GAS involving 187 distinct genetic variants were analyzed and cataloged in CUMAGAS-OSTEO, a Web-based information system (http://biomath.med.uth.gr) that allows the retrieval and synthesis of data from GAS on osteoarthritis. In individual studies, 66 variants (mostly single nucleotide polymorphisms) showed significant associations with osteoarthritis risk. For 19 variants, the association was significant at P < 0.01, with an increased risk greater than 30%. Only 2.4% of studies had statistical power greater than 50% to detect a modest genetic effect. Nineteen variants were investigated by 4 or more studies, and their results were subjected to meta-analysis. Significant associations were derived for 2 variants (GDF5 rs143383, LRCH1 rs912428) in the main meta-analysis and for 2 other variants (TXNDC3 rs4720262, ESR1 rs2234693) in subgroup analysis by ethnicity or osteoarthritic body site. Heterogeneity ranged from none to high. In general, there was consistency of genetic effects across ethnic groups and body sites, and there was no differential magnitude of effect in large studies versus small studies. CUMAGAS-OSTEO may be a useful tool for identifying pertinent gene-osteoarthritis associations and providing an updated summary of risk effects.
对骨关节炎的遗传关联研究(GAS)的现状进行了全面和系统的评估。在 CUMAGAS-OSTEO 中分析和编目了 327 项涉及 187 个不同遗传变异的 GAS 的数据,这是一个基于网络的信息系统(http://biomath.med.uth.gr),允许检索和综合骨关节炎 GAS 的数据。在个体研究中,66 个变异(主要是单核苷酸多态性)与骨关节炎风险显著相关。对于 19 个变异,关联在 P < 0.01 时具有统计学意义,风险增加超过 30%。只有 2.4%的研究具有大于 50%的统计效力来检测适度的遗传效应。有 19 个变异被 4 项或更多的研究进行了研究,其结果进行了荟萃分析。在主要荟萃分析中得出了 2 个变异(GDF5 rs143383、LRCH1 rs912428)的显著关联,在按种族或骨关节炎病变部位进行的亚组分析中得出了另外 2 个变异(TXNDC3 rs4720262、ESR1 rs2234693)的显著关联。异质性从无到高不等。总体而言,遗传效应在不同种族和病变部位之间具有一致性,并且在大型研究与小型研究之间不存在效应大小的差异。CUMAGAS-OSTEO 可能是识别相关基因-骨关节炎关联并提供风险效应最新总结的有用工具。