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Correlation Study Between Il-28B Gene Polymorphism (Rs8099917snp) and Sustained Virological Response in Iranian Patients With Chronic Hepatitis C Publisher Pubmed



Larijani MS1 ; Sadat SM1 ; Nikbin M2 ; Talebi SS3 ; Javadi F1 ; Mohajel N4 ; Bolhassani A1 ; Daneshvar M1 ; Aghasadeghi MR1 ; Pouriayevali MH5 ; Mapar M1
Authors
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Authors Affiliations
  1. 1. Department of Hepatitis and AIDS, Pasteur Institute of Iran, No. 69, Pasteur Ave, Tehran, 1316943551, Iran
  2. 2. Iran Hepatitis Network, Tehran, Iran
  3. 3. Department of Biostatistics and Epidemiology, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Virology, Pasteur Institute of Iran, Tehran, Iran
  5. 5. Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran

Source: Clinical Laboratory Published:2016


Abstract

Background: The current standard treatment for hepatitis C is a combination of pegylated interferon alpha and ribavirin (peg-IFNα/RBV). Recent studies have shown that single nucleotide polymorphisms (SNPs) near the in-terleukin 28B (IL28B) gene coding for IFN-X3 were associated with the antiviral treatment response. Therefore, in this study, we determined the distribution of the rs8099917 (T/G) polymorphism with sustained virological response (SVR) to chronic hepatitis C virus infection among Iranian patients. Methods: This cross-sectional study was performed on 150 blood samples based on 93 patients with chronic HCV genotypes 1 and 3 including 71 SVR positive, 22 negative, and 57 healthy individual controls. DNA was extracted from the samples and the frequency of the polymorphism was analyzed the using PCR-RFLP method. Finally, the products were detected on 3.5% agarose gel electrophoresis. Results: The analysis of the data for G/T polymorphism showed that the GG genotype was identified in 6 patients of 71 who achieved SVR, while the GT heterozygous was found in 33 patients and SVR was achieved in 19. Finally, the TT was detected in 53 patients and 7 patients were resistant to treatment. Conclusions: The results showed significant effects of G allele carriers on susceptibility to HCV infection compared to the other allele (T) in our studied population (p = 0.013, OR = 2.23, 95% CI = 1.18 - 4.21), but we did not find a significant correlation for SVR to therapy in patients with genotype TT (p = 0.055, OR = 0.48, 95% CI = 0.23-1.01). However, further studies with more samples are necessary.
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