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Significance of IL-1Ra and IL-6 gene variants in Turkish patients with Crimean-Congo hemorrhagic fever

机译:IL-1Ra和IL-6基因变异在土耳其克里米亚-刚果出血热患者中的意义

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Objective: To investigate the association between IL-1 Ra variable number of tandem repeat(rs2234663), IL-6-597 GA(rs1800797), IL-6-572 GC(rs1800796) and the risk of CrimeanCongo hemorrhagic fever(CCHF) in the Turkish patients. Methods: This study included 50 patients infected with CCHF and 50 healthy controls. These variants were genotyped using polymerase chain reaction and/or restriction fragment length polymorphism method. Results: The distribution of the IL-6-572 GC genotypes and alleles varied significantly between the patients and the controls. The subjects carrying IL-6-572 GC GG genotype and G allele had increased risk of developing CCHF compared to the control group(P=0.006, P=0.014, respectively). IL-6-572 GC GC genotype was higher in the controls than the patients(P=0.006). For the triple genotype combinations, the 1/2-GC-GG genotype combination was detected more frequently in the control group than CCHF patients(P=0.016). IL-6(-572/-597) GG-GG genotype was significantly higher in the patient group(P=0.015), while the GC-GG genotype was significantly lower in the patient group(P=0.005). Additionally, the G-G haplotype was significantly higher in the patient group(P=0.042), whereas C-G was found to be significantly lower in the patients than the control group(P=0.037). Conclusions: The results of this study suggest the IL-6-572 GC variant might be genetic markers of sensitivity to CCHF in the Turkish population and may facilitate greater protection against the disease.
机译:目的:探讨IL-1 Ra可变串联重复序列(rs2234663),IL-6-597 GA(rs1800797),IL-6-572 GC(rs1800796)与克里米亚刚果出血热(CCHF)风险的关系。土耳其病人。方法:本研究包括50例CCHF感染患者和50例健康对照。使用聚合酶链反应和/或限制性片段长度多态性方法对这些变体进行基因分型。结果:IL-6-572 GC基因型和等位基因在患者和对照组之间的分布差异很大。与对照组相比,携带IL-6-572 GC GG基因型和G等位基因的受试者发生CCHF的风险增加(分别为P = 0.006,P = 0.014)。 IL-6-572 GC的GC基因型在对照组中高于患者(P = 0.006)。对于三重基因型组合,对照组中比CCHF患者更频繁地检测到1 / 2-GC-GG基因型组合(P = 0.016)。 IL-6(-572 / -597)GG-GG基因型在患者组中显着较高(P = 0.015),而GC-GG基因型在患者组中显着较低(P = 0.005)。另外,患者组中的G-G单倍型显着更高(P = 0.042),而患者中的C-G显着低于对照组(P = 0.037)。结论:这项研究的结果表明,IL-6-572 GC变体可能是土耳其人群对CCHF敏感的遗传标记,并可能有助于更好地保护该病。

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