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Effects of receptor activator nuclear factor κB gene polymorphisms on the susceptibility to knee osteoarthritis

机译:受体激活因子核因子κB基因多态性对膝骨性关节炎的敏感性

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摘要

The present study aimed to explore genetic association of receptor activator nuclear factor κB (RANK) polymorphisms with individual susceptibility to knee osteoarthritis (OA) in different Kellgren–Lawrence (KL) grades.This case–control study included 138 knee OA patients and 145 healthy individuals. RANK rs1805034 and rs8086340 polymorphisms were genotyped through polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The effects of RANK polymorphisms on knee OA risk were analyzed via χ2 test or Fisher exact test, and the results were expressed using odds ratios (ORs) with corresponding 95% confidence intervals (CIs).The C allele of rs1805034 polymorphism had significantly higher frequency in knee OA patients than in controls (P = .044), indicating that this allele could increase the risk of knee OA (OR = 1.424, 95% CI = 1.010–2.008). Besides, the CC genotype and C allele of the rs1805034 polymorphism were significantly associated with elevated risk of knee OA in moderate grade (CC vs TT: P = .018, OR = 3.071, 95% CI = 1.187–7.941; C vs T: P = .012, OR = 1.787, 95% CI = 1.131–2.823). However, rs8086340 polymorphism had no significant association with knee OA riskThe C allele of RANK rs1805034 polymorphism is closely correlated with increased risk of knee OA, especially for moderate grade.
机译:本研究旨在探讨在不同的Kellgren-Lawrence(KL)等级中,受体激活因子核因子κB(RANK)多态性与个体对膝骨关节炎(OA)的易感性的遗传关联。该病例对照研究包括138例膝OA患者和145例健康人个人。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对RANK rs1805034和rs8086340多态性进行基因分型。通过χ 2 检验或Fisher精确检验分析RANK多态性对膝骨OA风险的影响,并使用具有95%置信区间(CI)的比值比(OR)表示结果。 rs1805034基因多态性的等位基因在膝OA患者中的频率显着高于对照组(P = .044),表明该等位基因可能增加膝OA的风险(OR = 1.424,95%CI = 1.010-2.008)。此外,rs1805034多态性的CC基因型和C等位基因与中度膝OA风险升高显着相关(CC vs TT:P = .018,OR = 3.071,95%CI = 1.187-7.941; C vs T: P = .012,OR = 1.787,95%CI = 1.131–2.823)。然而,rs8086340多态性与膝OA风险无显着相关性。RANK rs1805034多态性的C等位基因与膝OA风险增加密切相关,特别是对于中度等级。

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