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首页> 外文期刊>Molecular biology reports >Association of NADPH oxidase p22phox gene C242T, A640G and-930A/G polymorphisms with primary knee osteoarthritis in the Greek population
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Association of NADPH oxidase p22phox gene C242T, A640G and-930A/G polymorphisms with primary knee osteoarthritis in the Greek population

机译:NADPH氧化酶p22phox基因C242T,A640G和-930A / G多态性与希腊人群原发性膝骨关节炎的关系

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摘要

Osteoarthritis (OA) is the most common form of arthritis with still unknown pathogenic etiology and considerable contribution of genetic factors. Recently, a new emerging role of oxidative stress in the pathology of OA has been reported, lacking however elucidation of the underlying mechanism. Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase being a complex enzyme produced by chondrocytes, presents the major source of reactive oxygen species and main contributor of increased oxidative stress. The present study aims to evaluate the association of NADPH oxidase p22phox gene C242T, A640G and -A930G polymorphisms with primary knee OA in the Greek population. One hundred fifty five patients with primary symptomatic knee OA participated in the study along with 139 matched controls. Genotypes were determined using polymerase chain reaction and restriction fragment length polymorphism technique. Allelic and genotypic frequencies were compared between both study groups. NADPH p22phox -A930G polymorphism was significantly associated with knee OA in the crude analysis (P = 0.018). No significant difference was detected for C242T and A640G polymorphisms (P > 0.05). The association between -A930G polymorphism and knee OA disappeared when the results were adjusted for obesity (P = 0.078, odds ratio 0.54, 95 % CI 0.272-1.071). The interaction between all three polymorphisms was not significant. The present study shows that NADPH oxidase p22phox gene C242T, A640G and -A930G polymorphisms are not risk factors for knee OA susceptibility in the Greek population. Further studies are needed to give a global view of the importance of this polymorphism in the pathogenesis of OA.
机译:骨关节炎(OA)是关节炎的最常见形式,其病因仍未知,遗传因素也占相当大的比重。近来,已经报道了氧化应激在OA病理中的新的新兴作用,但是缺乏对潜在机制的阐明。烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶是软骨细胞产生的复合酶,是活性氧的主要来源,也是氧化应激增加的主要因素。本研究旨在评估希腊人口中NADPH氧化酶p22phox基因C242T,A640G和-A930G多态性与原发性膝骨关节炎的相关性。 155例原发性症状性膝骨关节炎患者和139名相匹配的对照组参加了研究。使用聚合酶链反应和限制性片段长度多态性技术确定基因型。在两个研究组之间比较了等位基因和基因型频率。在粗略分析中,NADPH p22phox -A930G多态性与膝骨关节炎显着相关(P = 0.018)。 C242T和A640G多态性未检测到显着差异(P> 0.05)。对肥胖症进行校正后,-A930G基因多态性与膝盖OA之间的关联消失了(P = 0.078,比值比为0.54,95%CI为0.272-1.071)。这三种多态性之间的相互作用并不显着。本研究表明,NADPH氧化酶p22phox基因C242T,A640G和-A930G多态性不是希腊人群膝OA易感性的危险因素。需要进行进一步的研究以全面了解这种多态性在OA发病机理中的重要性。

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