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Comparison of Three Different Methods for Detection of Il28 Rs12979860 Polymorphisms As a Predictor of Treatment Outcome in Patients With Hepatitis C Virus Publisher



Fateh A1, 2 ; Aghasadeghi M3 ; Siadat SD1 ; Vaziri F1 ; Sadeghi F4 ; Fateh R5 ; Keyvani H6 ; Tasbiti AH1 ; Yari S1 ; Ataeipirkooh A6 ; Monavari SH6
Authors
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Authors Affiliations
  1. 1. Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran
  2. 2. Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran
  4. 4. Department of Immunology and Microbiology, Babol University of Medical Sciences, School of Medicine, Babol, Iran
  5. 5. Department of Microbiology and Immunology, Faculty of Medicine, Qom University of Medical Sciences, Qom, Iran
  6. 6. Department of Virology, Iran University of Medical Sciences, Tehran, Iran

Source: Osong Public Health and Research Perspectives Published:2016


Abstract

Objectives: This study aimed to evaluate the specificity, sensitivity, cost, and turn-around time of three methods of gene polymorphism analysis and to study the relationship between IL28B rs12979860 and SVR rate to pegIFN-α/RVB therapy among patients with chronic hepatitis C. Methods: A total of 100 samples from chronic hepatitis C patients were analyzed in parallel using the three methods: direct sequencing, real-time polymerase chain reaction (PCR), amplification refractory mutation system (ARMS)-PCR. Results: The different profiles for IL28B rs12979860 alleles (CC, CT, and TT) obtained with PCR-RFLP, ARMS-PCR, and direct sequencing were consistent among the three methods. Prevalence of rs12979860 genotypes CC, CT and TT in HCV genotype 1a was 10(19.6%), 35(68.6%), and six (11.8%), respectively, and in HCV genotype 31, it was 13(26.5%), 31(63.3%), and five (10.2%), respectively. No significant difference was seen between rs12979860 genotype and HCV genotype (p = 0.710). Conclusion: Screening by ARMS - PCR SNOP detection represents the most efficient and reliable method to determine HCV polymorphisms in routine clinical practice. © 2016.
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