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Potential Influence of Interleukin-1 Receptor Antagonist Gene Polymorphism on Knee Osteoarthritis Risk

机译:白介素1受体拮抗剂基因多态性对膝骨关节炎风险的潜在影响

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Objectives:Genes encoding for cytokines have been associated with susceptibility for joint osteoarthritis (OA) and interleukin (IL)-1 gene is supposed to be involved in the cartilage destruction process. In this regard, interleukin-1 receptor antagonist (IL-1RA) competing with IL-1 for binding to its receptor may act as an inhibitor of cartilage breakdown. We assessed the association of primary knee OA with IL-1RA region as a putative factor of susceptibility to knee OA in Egyptian patients.Design and methods:Eighty patients with primary knee OA and 40 aged-matched healthy controls were included into the study. DNA samples were used to study genotypes of IL-1RN gene by polymerase chain reaction (PCR) in both groups.Results:An increased frequency of the IL-1RN*1 and IL-1RN*2 alleles was found in OA patients relative to controls (60.5% vs. 39.5%,P= 0.039, 85.4% vs. 14.6%,P= 0.002, respectively) however, only the carriage rate of IL-1RN*2 allele was found to be significant when OA patients were compared to the controls. Significant higher frequencies of IL-1RN*1/*2 and IL-1RN*2/*2 genotypes in OA patients were observed as compared with controls. Both visual analogue scale (VAS) and radiographic score revealed significant correlation with both the allelic frequency and the carriage rate of IL-1RN*2 allele. Moreover, absolute frequency of IL-1RN*1/*2 genotype OA patients revealed severe VAS and high radiographic score.Conclusion:These results suggest that IL-1RN*2 allele represent a significant factor influencing the severity and course of knee OA; thereby supporting the potential role of IL-1 in the pathogenesis of this disease.
机译:目的:编码细胞因子的基因与关节骨关节炎(OA)的易感性有关,并且白介素(IL)-1基因可能参与了软骨破坏过程。在这方面,与IL-1竞争结合其受体的白介素-1受体拮抗剂(IL-1RA)可以作为软骨破坏的抑制剂。我们评估了原发性膝骨关节炎与IL-1RA区域之间的关联,作为埃及患者对膝骨关节炎的易感性的推定因素。设计和方法:80例原发性膝骨关节炎和40位年龄相匹配的健康对照组被纳入研究。两组患者的DNA样本均通过聚合酶链反应(PCR)研究IL-1RN基因的基因型。结果:与对照组相比,OA患者中IL-1RN * 1和IL-1RN * 2等位基因的频率增加(分别为60.5%和39.5%,P = 0.039,85.4%vs. 14.6%,P = 0.002),但是与OA患者相比,仅IL-1RN * 2等位基因的携带率显着。控制。与对照组相比,在OA患者中观察到IL-1RN * 1 / * 2和IL-1RN * 2 / * 2基因型显着更高的频率。视觉模拟量表(VAS)和射线照相评分均显示与IL-1RN * 2等位基因的等位基因频率和携带率显着相关。此外,IL-1RN * 1 / * 2基因型OA患者的绝对频率显示出严重的VAS和放射学评分较高。结论:这些结果表明IL-1RN * 2等位基因是影响膝OA严重程度和病程的重要因素。从而支持IL-1在这种疾病的发病机理中的潜在作用。

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