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Association of tumor necrosis factor alpha-308 promoter polymorphism with spondyloarthritides patients in Colombia

机译:哥伦比亚肿瘤性坏死因子α-308启动子多态性与脊椎关节炎相关性

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摘要

The pathogenesis of SpA is considered to be a complex and multi-factorial process and, similar to other autoimmune diseases, includes the activity of proinflammatory cytokines such as TNF alpha. Our study compared the -308 promoter polymorphism of TNF alpha with TNF alpha levels, HLA-B27 status, age at the onset of symptoms, SpA subtype and the clinical degree of activity in Colombian SpA patients and healthy subjects (HS). Comparisons of the TNF alpha-308A genotype among HS and SpA patients (P = 0.004), uSpA patients (P = 0.040), ReA patients (P = 0.001), were significantly different and AS patients (P = 0.110), as were alleles for SpAs (P = 0.007) between patients with SpAs and controls. Initial exploratory analyses demonstrated that the TNF alpha-308 SNP genotype frequencies were different among SpA patients and HS in the Colombian population studied. Furthermore, there was no significant correlation with activity and functional clinical index, serum TNF alpha level or HLA B27 status. Allele frequencies, on the other hand, were correlated with the activity clinical index.
机译:SpA的发病机理被认为是一个复杂的多因素过程,与其他自身免疫性疾病相似,它包括促炎细胞因子(如TNFα)的活性。我们的研究在哥伦比亚SpA患者和健康受试者(HS)中比较了TNFα的-308启动子多态性与TNFα水平,HLA-B27状态,症状发作的年龄,SpA亚型以及临床活动程度。 HS和SpA患者(P = 0.004),uSpA患者(P = 0.040),ReA患者(P = 0.001)之间的TNF alpha-308A基因型比较与AS患者(P = 0.110)显着不同SpAs患者与对照组之间SpA的差异(P = 0.007)。初步的探索性分析表明,在哥伦比亚研究人群中,SpA患者和HS之间的TNF alpha-308 SNP基因型频率不同。此外,与活性和功能性临床指标,血清TNFα水平或HLA B27状态无显着相关性。另一方面,等位基因频率与活动性临床指标相关。

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