Chemokine and chemokine receptor gene polymorphism in Tunisian hemodialysis patients with HCV infection.

Leila Ksiaa Cheikh Rouhou, Yousr Lakhoua Gorgi, Hajer Aounallah Skhiri, Houda Aouadi, Salwa Jendoubi Ayed, Imen Sfar, Khaled Ayed, Taieb Ben Abdallah
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引用次数: 10

Abstract

Introduction: Our aim was to investigate the possibility of a significant relationship between chemokines and chemokine receptor genes polymorphisms and the spontaneous clearance or the persistence of HCV infection.

Methods: A total of 96 hemodialysis (HD) patients infected with HCV were classified into two groups: G1 included 73 patients with persistently positive HCV-RNA and G2 included 23 HD patients who have spontaneously eliminated the virus. The control group consisted of 170 healthy blood donors. All subjects were genotyped for CCR5 ?32, CCR5 (-59029) A/G, CCR2 (64Ile) and MCP-1(-2518) A/G gene polymorphisms.

Results: Our results showed a statistically significant increased frequencies of the CCR2 (64Ile) and the (-59029) CCR5 A alleles in patients infected with HCV (22.1% and 35.9%) compared to G1 (24.3% and 40.6%) and compared to controls (14.4% and 20%). We also observed a lower frequency of the MCP-1 G allele and a greater frequency of the CCR5?32 variant in G2 (15.2% and 6.5%) compared to G1 (22.6% and 1.4%) that was not statistically significant. However, adjustment for known covariates (age, gender and HCV genotypes) didn't confirm the results of univariate analysis.

Conclusion: In conclusion, our study suggests a possible role for some of the studied chemokines polymorphisms in the spontaneous clearance or persistence of HCV infection in Tunisian population. These results should be further investigated by a prospective cohort studies and large population-based studies.

突尼斯血液透析患者HCV感染的趋化因子和趋化因子受体基因多态性。
简介:我们的目的是研究趋化因子和趋化因子受体基因多态性与HCV感染的自发清除或持续之间的显著关系的可能性。方法:将96例感染HCV的血液透析(HD)患者分为两组:G1组包括73例HCV- rna持续阳性患者,G2组包括23例自行消除病毒的HD患者。对照组由170名健康的献血者组成。对所有受试者进行CCR5 - 32、CCR5 (-59029) A/G、CCR2 (64Ile)和MCP-1(-2518) A/G基因多态性基因分型。结果:我们的研究结果显示,与G1(24.3%和40.6%)和对照组(14.4%和20%)相比,HCV感染患者的CCR2 (64Ile)和(-59029)ccr5a等位基因频率(22.1%和35.9%)有统计学意义的增加。我们还观察到mcp - 1g等位基因的频率较低,而CCR5?G2组有32个变异(15.2%和6.5%),G1组有22.6%和1.4%,差异无统计学意义。然而,调整已知协变量(年龄、性别和HCV基因型)并不能证实单变量分析的结果。结论:总之,我们的研究表明,在突尼斯人群中,一些被研究的趋化因子多态性可能在HCV感染的自发清除或持续中起作用。这些结果应该通过前瞻性队列研究和大规模人群研究来进一步调查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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