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首页> 外文期刊>Clinical rheumatology >The single-nucleotide polymorphism (SNP) of tumor necrosis factor alpha-308G/A gene is associated with early-onset primary knee osteoarthritis in an Egyptian female population
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The single-nucleotide polymorphism (SNP) of tumor necrosis factor alpha-308G/A gene is associated with early-onset primary knee osteoarthritis in an Egyptian female population

机译:肿瘤坏死因子α-308g / A基因的单核苷酸多态性(SNP)与埃及女性人口的早发初级膝关节骨关节炎有关

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摘要

The objective of the present study is to investigate if there is a potential association between the single-nucleotide polymorphisms (SNPs) of the tumor necrosis factor alpha gene (TNF-alpha -308G/A, rs1800629) and the susceptibility to and severity of early-onset knee osteoarthritis in the Egyptian female population. Genotype distributions and allelic frequencies of TNF-alpha -308G/A polymorphism were investigated in 210 knee osteoarthritis (OA) patients and 210 age-, sex-, and ethnicity-matched healthy controls (HC). Polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP) amplifications were implemented to determine TNF-alpha -308G/A SNP. Serum and synovial fluid levels of TNF-alpha, besides ESR and CRP, as laboratory markers for inflammation, were estimated for all patients and HC. Plain X-ray as well as MRI knee was done for grading of OA. Disease severity was estimated by Western Ontario and McMaster University Osteoarthritis scores. Percentages of TNF-alpha-G308A genotypes GG, AG, and AA were 85.7, 11.9, and 2.4% in OA patients and 54.7, 39.1, and 6.2% in controls, respectively. The frequencies of the GG genotype and G allele were significantly higher in subjects with knee OA than in HC (P = 0.04 and P < 0.001, respectively). Logistic regression analysis showed that the GG genotype and G allele are independently associated with increased risk for knee OA (odds ratio = 3.13, 95% confidence interval = 1.04-9.39, P = 0.04 for GG genotype, and odds ratio = 3.81, 95% confidence interval = 2.52-5.76, P = 0.001 for G allele). There is a close relationship between TNF-alpha-G308A polymorphism and individual susceptibility to and severity of early-onset knee OA in the Egyptian females.
机译:本研究的目的是研究肿瘤坏死因子α基因的单核苷酸多态性(SNP)之间是否存在潜在关联(TNF-α-308G / A,1800629)以及早期的易感性和严重程度埃及女性人口中的膝关节骨关节炎。在210膝骨关节炎(OA)患者和210名年龄,性别和种族匹配的健康对照中研究了TNF-α-308G / A多态性的基因型分布和等位基因频率。实施聚合酶链反应限制的片段长度多态性(PCR-RFLP)扩增以确定TNF-α-308g / A SNP。除ESR和CRP之外,TNF-α的血清和滑膜液水平估计为炎症的实验室标志物,所有患者和HC都估计。普通X射线以及MRI膝关节是为了评级OA而完成的。疾病严重程度估计,估计西部的安大略省和麦克马斯特大学骨关节炎分数。在OA患者中,TNF-α-G308A基因型GG,AG和AA的百分比分别为85.7,11.9和2.4%,分别为54.7,39.1和6.2%。 GG基因型和G等位基因的频率在膝关节OA的受试者中显着高于HC(P = 0.04和P <0.001)。 Logistic回归分析表明,GG基因型和G等位基因与膝关节OA的风险不同(差距= 3.13,95%置信区间= 1.04-9.39,P = 0.04,对于GG基因型,= 3.81,95%置信区间= 2.52-5.76,p = 0.001,g等位基因)。 TNF-alpha-G308A多态性与埃及女性早起膝关节OA的个人敏感性之间存在密切的关系。

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