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The genetic association of cytokine genes, single nucleotide polymorphisms, and the incidence of liver cirrhosis in chronic hepatitis C Egyptian patients

机译:细胞因子基因,单核苷酸多态性和肝硬化在慢性丙型肝炎患者肝硬化发病率的遗传结合

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Abstract Cytokines play a central role in regulating the anti-viral responses against hepatitis C virus (HCV). The objective of this study were to evaluate the effect of proinflammatory cytokines (IL-18 ??607 C/A, rs 1946518; IL-18 ??137 G/C, rs 187283; INF-γ +?874 T/A, rs 240561), SNPs, and the anti-inflammatory cytokine (IL-10 +?1082 G/A, rs 1800896) SNPs on the risk of development of hepatic cirrhosis in Egyptian patients and to evaluate the combined effect of the polymorphic variants that show an interrelation with the risk of hepatic cirrhosis. The study included 63 chronic HCV patients. The patients were stratified into two groups. Group 1 consisted of 33 cirrhotic chronic hepatitis C patients while the second group consisted of 30 non-cirrhotic chronic hepatitis C patients that were taken as a control group. Genotyping of IFN-γ (+?874 T/A) and IL-10 (??1082 G/A) SNPs was performed by allele-specific PCR technique (AS-PCR). Genotyping of IL-18 (??607 C/A) and IL-18 (??137 G/C) SNPs was determined by PCR-RFLP technique. Analysis of IFN-γ (+?874 T/A) SNP revealed that the T allele and the TT genotype were significantly higher in cirrhotic patients’ group compared to non-cirrhotic group ( P ? P ?=?0.004, respectively). Analysis of IL-10 (??1082 G/A) SNP revealed that the A allele and AA genotype were significantly higher in the cirrhotic patients’ group ( P ?=?0.001 and P ?=?0.047, respectively). Regression analysis revealed that IFN-γ Hi/IL-10 Lo combined genotypes were significantly higher in liver cirrhosis patients compared to non-cirrhotic patients ( P ?=?0.002). INF-γ (+?874 T/A) and IL-10 (+?1082 G/A) SNPs might be associated with occurrence of hepatic cirrhosis in chronic HCV Egyptian patients.
机译:摘要细胞因子在调节对丙型肝炎病毒(HCV)的抗病毒反应方面发挥着核心作用。本研究的目的是评估促炎细胞因子的影响(IL-18 ?? 607 C / A,1946518卢比; IL-18 ?? 137 G / C,RS 187283; INF-γ+?874 T / A, 240561),SNP和抗炎细胞因子(IL-10 +?1082克/ A,1800896卢比)SNP,埃及患者肝硬化的发展风险,评价显示的多态变异的综合作用一种与肝硬化风险的相互关系。该研究包括63例慢性HCV患者。患者分为两组。第1组由33次肝硬化慢性丙型肝炎患者组成,而第二组由30名非肝硬化慢性丙型肝炎患者组成,该患者作为对照组。通过等位基因特异性PCR技术(AS-PCR)进行IFN-γ(+α874t/ a)和IL-10(Δω10g/ a)SNP的基因分型。通过PCR-RFLP技术测定IL-18(Δε307c/ a)和IL-18(Δε13/ c)SNP的基因分型。 IFN-γ(+α874T/ A)SNP的分析显示,与非肝硬化组相比,肝硬化患者组的T等位基因和TT基因型显着高(P?P?= 0.004)。 IL-10(1082g / a)SNP的分析显示,肝硬化患者组(p?= 0.001和p≤0.047)显着升高。回归分析显示,与非肝硬化患者相比,IFN-γHI / IL-10 LO组合基因型在肝硬化患者中显着较高(P?= 0.002)。 INF-γ(+α874t/ a)和IL-10(+ 1082g / a)SNP可能与慢性HCV埃及患者肝硬化的发生相关。

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