Author/Authors :
Sporea, Ioan Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Popescu, Alina Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Curescu, Manuela Department of Infectious Diseases - University of Medicine and pharmacy - Timisoara, Romania , Sirli, Roxana Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Dan, Isabel Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Goldis, Adrian Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Gradinaru, oana Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Ardelean, Melania Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Danila, Mirela Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Bota, Simona Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania , Deleanu, Alexandra Department of Gastroenterology and Hepatology - University of Medicine and pharmacy - Timisoara, Romania
Abstract :
Background: Multiple variables influencing the sustained virologic response (SVR) in
chronic hepatitis C have been evaluated. one of them is genetic polymorphism near the
IL28B gene.
Objectives: The aim of this study was to evaluate the influence of IL28B genotypes on SVR
rates in a group of patients with chronic hepatitis C from the western part of Romania.
Patients and Methods: A retrospective study was performed in 107 consecutive patients,
previously treated with standard-of-care medication for chronic hepatitis C, identified
from the databases of 2 centers. Patient demographics, viral load before treatment and
at 12, 24, and 72 weeks from the treatment start, and IL28B genotype were evaluated.
Results: Among the 107 patents in the study group, 54 patients had SVR (50.5%), and 62
(57.9%) showed a complete early virologic response (ceVR). The SVR rates according to
IL28B genotype were as follows: 73.1% in patients with genotype C/C, 40.9% in those with
genotype C/T, and 57.1% in those with genotype T/T (i.e., 73.1% among patients with the
C/C genotype vs. 43.7% among those with non-C/C genotypes; P = 0.0126). The ceVR rates
were 80.8% in patients with the C/C genotype vs. 51.2% in those with non-C/C genotypes
(P = 0.011).
Conclusions: In our cohort of 107 Caucasian HCV patients, the SVR rate was 50.5% with
standard-of-care treatment. The SVR rate was directly related to the IL28B genotype: 73.1%
in the C/C genotype vs. 43.7% in non-C/C genotypes (P = 0.0126).
Keywords :
Genetic Variation , IL28B Protein , Human , Hepatitis C , Chronic