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脂联素+276G/T多态性与膝关节骨关节炎的关联

Association of adiponectin +276G/T polymorphism with knee osteoarthritis.

作者信息

Zhan Dong, Yuktanandana Pongsak, Anomasiri Wilai, Tanavalee Aree, Honsawek Sittisak

机构信息

Department of Biochemistry, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.

Department of Orthopaedics, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.

出版信息

Biomed Rep. 2014 Mar;2(2):229-232. doi: 10.3892/br.2014.228. Epub 2014 Jan 20.

Abstract

Osteoarthritis (OA) is a prevalent, degenerative joint disorder leading to the destruction of articular cartilage, osteophyte formation and subchondral bone sclerosis. Genetic and environmental factors are involved in the development of OA. The role of adiponectin gene polymorphisms in OA has not yet been established. The aim of this study was to investigate the association of adiponectin +276G/T (rs1501299) gene polymorphism with knee OA. Genotype distributions and allelic frequencies of adiponectin gene, +276G/T polymorphism were determined in a total of 200 subjects (100 knee OA patients and 100 healthy controls). Single-nucleotide polymorphism (SNP) of the adiponectin +276G/T gene was genotyped by polymerase chain reaction (PCR)-restriction fragment length polymorphism analysis. The genotype distribution of +276G/T SNP was observed in the Hardy-Weinberg equilibrium for OA patients and controls. No statistically significant difference was identified between the two groups with respect to genotype distributions and allelic frequencies (P>0.05). The T- and G-allele frequencies were indicated as 24.5 and 75.5%, respectively, in OA patients, whereas the frequency was 23-70% in the control group. Findings of this study therefore suggest that the +276G/T SNP was not associated with susceptibility to knee OA.

摘要

骨关节炎(OA)是一种常见的退行性关节疾病,可导致关节软骨破坏、骨赘形成和软骨下骨硬化。遗传和环境因素参与了OA的发病过程。脂联素基因多态性在OA中的作用尚未明确。本研究旨在探讨脂联素+276G/T(rs1501299)基因多态性与膝关节OA的相关性。在总共200名受试者(100名膝关节OA患者和100名健康对照)中确定了脂联素基因+276G/T多态性的基因型分布和等位基因频率。采用聚合酶链反应(PCR)-限制性片段长度多态性分析对脂联素+276G/T基因的单核苷酸多态性(SNP)进行基因分型。OA患者和对照组中+276G/T SNP的基因型分布符合Hardy-Weinberg平衡。两组在基因型分布和等位基因频率方面未发现统计学显著差异(P>0.05)。OA患者中T等位基因和G等位基因频率分别为24.5%和75.5%,而对照组中该频率分别为23%和70%。因此,本研究结果表明+276G/T SNP与膝关节OA的易感性无关。

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Current concepts in the pathogenesis of osteoarthritis.骨关节炎发病机制的当前概念。
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