TY - JOUR
T1 - Predominance of hepatitis C virus Q80K among NS3 baseline-resistance-associated amino acid variants in direct-antiviral-agent-naïve patients with chronic hepatitis
T2 - single-centre experience
AU - Ruggiero, Tina
AU - Proietti, Alex
AU - Boglione, Lucio
AU - Milia, Maria Grazia
AU - Allice, Tiziano
AU - Burdino, Elisa
AU - Orofino, Giancarlo
AU - Bonora, Stefano
AU - Di Perri, Giovanni
AU - Ghisetti, Valeria
N1 - Publisher Copyright:
© 2015, Springer-Verlag Wien.
PY - 2015/8/7
Y1 - 2015/8/7
N2 - In the era of direct-acting antiviral agents (DAAs), hepatitis C virus (HCV) genotyping tests at baseline are controversial. The HCV NS3-Q80K polymorphism is associated with resistance to the recently approved NS3 inhibitor simeprevir (SMV) when combined with PEG-interferon and ribavirin (PEG-IFN/RBV) and alternative therapy should be considered for patients with baseline Q80K. The aim of this study was to provide an estimate of Q80K prevalence at baseline in a study group of 205 DAA-naïve patients (21 % of them with HIV coinfection) using NS3 full-population direct sequencing to detect resistance-associated amino acid variants (RAVs). NS3 RAVs were identified in 56 patients (27.3 %). Q80K was the most frequently reported one (41 %), in both HIV/HCV-coinfected and HCV-monoinfected patients, but it was only detectable in cases of HCV-subtype 1a infection. Therefore, in clinical practice, an NS3-Q80K genotyping test prior to simeprevir plus PEG-IFN/RBV treatment is highly recommended.
AB - In the era of direct-acting antiviral agents (DAAs), hepatitis C virus (HCV) genotyping tests at baseline are controversial. The HCV NS3-Q80K polymorphism is associated with resistance to the recently approved NS3 inhibitor simeprevir (SMV) when combined with PEG-interferon and ribavirin (PEG-IFN/RBV) and alternative therapy should be considered for patients with baseline Q80K. The aim of this study was to provide an estimate of Q80K prevalence at baseline in a study group of 205 DAA-naïve patients (21 % of them with HIV coinfection) using NS3 full-population direct sequencing to detect resistance-associated amino acid variants (RAVs). NS3 RAVs were identified in 56 patients (27.3 %). Q80K was the most frequently reported one (41 %), in both HIV/HCV-coinfected and HCV-monoinfected patients, but it was only detectable in cases of HCV-subtype 1a infection. Therefore, in clinical practice, an NS3-Q80K genotyping test prior to simeprevir plus PEG-IFN/RBV treatment is highly recommended.
UR - http://www.scopus.com/inward/record.url?scp=84946490901&partnerID=8YFLogxK
U2 - 10.1007/s00705-015-2563-3
DO - 10.1007/s00705-015-2563-3
M3 - Article
SN - 0304-8608
VL - 160
SP - 2881
EP - 2885
JO - Archives of Virology
JF - Archives of Virology
IS - 11
ER -