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Interferon Responsiveness in Patients Infected with Hepatitis C Virus 1b Differs Depending on Viral Subtype

Overview
Journal Gut
Specialty Gastroenterology
Date 2001 Jul 17
PMID 11454804
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Abstract

Background: Genotype 1b of hepatitis C virus (HCV) comprises mainly three subtypes, each named for its geographic prevalence (worldwide, W; Japan, J; and not in Japan, NJ).

Aim: To characterise the newly identified subtypes of genotype 1b and to review factors associated with response to interferon (IFN) for each subtype.

Patients: Chronic hepatitis patients (80 men and 41 women; mean age 48.5 years, range 20.7--69.3) with HCV genotype 1b (W type, n=41; J type, n=38) or genotype 2a (n=42) were treated according to the same IFN protocol. Forty four patients (36.4%) negative for serum HCV RNA six months after cessation of treatment were considered complete responders.

Methods: Factors associated with complete response were investigated.

Results: Genotype 2a patients had lower viral loads (odds ratio 0.11 (95% confidence intervals (CI) 0.049--0.256)) and a better IFN response (odds ratio 0.25 (95% CI 0.117--0.552)) than genotype 1b patients whereas W type and J type patients had similar viral loads and responses to IFN. IFN response in W type patients was associated with female sex (odds ratio 0.23 (95% CI 0.055--0.983)) and low viral load (odds ratio 84.00 (95% CI 14.04--502.6)) whereas response in J type patients was related to transfusion history (odds ratio 7.20 (95% CI 1.443--35.91)), low viral load (odds ratio 117.0 (95% CI 17.82--768.3)), and genetic mutation in the interferon sensitivity determining region of the virus (odds ratio 0.08 (95% CI 0.013--0.553)). Multivariate analysis found low viral load (odds ratio 64.19 (95% CI 14.66--281.06)) to be the only significant independent factor associated with IFN response.

Conclusions: Factors associated with IFN responsiveness in HCV infection differ with viral subtype.

References
1.
Watson J, Brind A, Chapman C, Bates C, Gould F, Johnson S . Hepatitis C virus: epidemiology and genotypes in the north east of England. Gut. 1996; 38(2):269-76. PMC: 1383036. DOI: 10.1136/gut.38.2.269. View

2.
Kobayashi M, Tanaka E, Sodeyama T, Urushihara A, Matsumoto A, Kiyosawa K . The natural course of chronic hepatitis C: a comparison between patients with genotypes 1 and 2 hepatitis C viruses. Hepatology. 1996; 23(4):695-9. DOI: 10.1053/jhep.1996.v23.pm0008666319. View

3.
Zein N, Rakela J, Krawitt E, Reddy K, Tominaga T, Persing D . Hepatitis C virus genotypes in the United States: epidemiology, pathogenicity, and response to interferon therapy. Collaborative Study Group. Ann Intern Med. 1996; 125(8):634-9. DOI: 10.7326/0003-4819-125-8-199610150-00002. View

4.
Poynard T, Leroy V, Cohard M, Thevenot T, Mathurin P, Opolon P . Meta-analysis of interferon randomized trials in the treatment of viral hepatitis C: effects of dose and duration. Hepatology. 1996; 24(4):778-89. DOI: 10.1002/hep.510240405. View

5.
Smith D, Pathirana S, Davidson F, Lawlor E, Power J, Yap P . The origin of hepatitis C virus genotypes. J Gen Virol. 1997; 78 ( Pt 2):321-8. DOI: 10.1099/0022-1317-78-2-321. View