Zhao Kun, Nie Liuyan, Chin Grace Min Jun, Ye Xiangming, Sun Peng
Department of Rehabilitation Medicine, Center for Rehabilitation Medicine, Rehabilitation and Sports Medicine Research Institute of Zhejiang Province, Zhejiang Provincial People's Hospital (Affiliated People's Hospital, Hangzhou Medical College), Hangzhou, China.
Department of Rheumatology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Front Med (Lausanne). 2022 Sep 23;9:1024750. doi: 10.3389/fmed.2022.1024750. eCollection 2022.
The association of fat mass and obesity-related () gene with osteoarthritis (OA) risk has been investigated in multiple genome-wide association studies but showed inconsistent results. Our study aimed to assess expression in different OA sequencing datasets and to meta-analyze whether polymorphism was associated with the risk of osteoarthritis.
Gene expression profiles were obtained from ArrayExpress, Gene Expression Omnibus (GEO), and BioProject databases. Three electronic databases including PubMed and EMBASE were systematically retrieved to identify articles exploring the association between polymorphisms and OA risk published before September 2022. Summary odds ratios (ORs) and corresponding 95% confidence intervals (95% CIs) were calculated to perform the result. Stata software was utilized to conduct analyses on predetermined ethnicity and gender subgroups and sensitivity.
gene was differentially expressed in the datasets from the UK. This systematic review and meta-analysis encompasses eight studies that revealed a significant association between polymorphisms and OA risk [OR 1.07, 95% CI (1.03, 1.11), < 0.001] in the overall population. In subgroup analysis, a marked association was observed in European Caucasian [OR 1.08, 95% CI (1.04-1.12), < 0.001] and North American Caucasian with the Asian subgroups [OR 0.98, 95% CI (0.83-1. 6), = 0.83] as an exception. Among the studies, four of them demonstrated attenuation in their OA risk after body mass index (BMI) adjustment in Caucasian populations.
significant differential expression was associated with the increased risk of OA in Caucasian populations. Nevertheless, the causality between polymorphisms and OA risk remains largely elusive. Hence, further studies with larger sample size are necessary to validate whether gene polymorphism contributes to OA susceptibility.
在多项全基因组关联研究中,已对脂肪量和肥胖相关()基因与骨关节炎(OA)风险之间的关联进行了调查,但结果不一致。我们的研究旨在评估不同OA测序数据集中的表达情况,并对多态性是否与骨关节炎风险相关进行荟萃分析。
从ArrayExpress、基因表达综合数据库(GEO)和生物项目数据库中获取基因表达谱。系统检索包括PubMed和EMBASE在内的三个电子数据库,以识别2022年9月之前发表的探索多态性与OA风险之间关联的文章。计算汇总比值比(OR)和相应的95%置信区间(95%CI)以得出结果。使用Stata软件对预先确定的种族和性别亚组以及敏感性进行分析。
基因在来自英国的数据集中存在差异表达。这项系统评价和荟萃分析涵盖了八项研究,这些研究表明在总体人群中多态性与OA风险之间存在显著关联[OR 1.07,95%CI(1.03,1.11),<0.001]。在亚组分析中,在欧洲白种人[OR 1.08,95%CI(1.04 - 1.12),<0.001]和北美北北美白种人中观察到显著关联,亚洲亚组除外[OR 0.98,95%CI(0.83 - 1.6),=0.83]。在这些研究中,其中四项研究表明,在白种人群体中调整体重指数(BMI)后,其OA风险有所降低。
显著的差异表达与白种人群体中OA风险增加相关。然而,多态性与OA风险之间的因果关系在很大程度上仍然难以捉摸。因此,需要进行更大样本量的进一步研究,以验证基因多态性是否会导致OA易感性。