Abstract
Objective. The results of a previous study suggest that an index calculated according to the formula (normalized ASAT×PK-INR)×100/thrombocyte count (×109/L; GUCI) may reflect liver fibrosis in patients with chronic hepatitis C virus (HCV) infection. The aims of the present study were (i) to validate the association between the Göteborg University Cirrhosis Index (GUCI) score and liver fibrosis and (ii) to evaluate the utility of this index in predicting the outcome of antiviral treatment. Material and methods. A total of 269 patients with chronic HCV infection, stratified according to HCV genotype (1/4 versus 2/3) participated in a phase III trial using pegylated interferon α-2a and ribavirin (DITTO study). Retrospective analyses of the baseline GUCI scores and assessments of pretreatment liver biopsies using the Ishak protocol were performed. Cut-off GUCI scores were calculated to distinguish patients with a high or low probability of sustained viral response (SVR). Results. Striking associations between GUCI and Ishak fibrosis stages (stages 0-2 versus stages 3-4, p=0.0002, stages 3-4 versus stages 5-6, p=0.002) were observed. In patients with genotype 1 or 4, a GUCI score below 0.33 was associated with a rapid viral response to antiviral treatment and an SVR rate of 80%. Ninety-two percent of patients (92/101) with a SVR had a pretreatment GUCI score below 1.11. Conclusions. Our results suggest that the GUCI score appropriately reflects the stage of liver fibrosis in HCV-infected patients, and predicts initial viral kinetics as well as treatment outcome in patients infected with HCV genotype 1 or 4.
Original language | English |
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Pages (from-to) | 73-80 |
Number of pages | 8 |
Journal | Scandinavian Journal of Gastroenterology |
Volume | 43 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2008 |
Bibliographical note
Funding Information:This study was supported by the European Community (QLK2-2000-00836), the Swedish Society Against Cancer (Cancerfonden), The Swedish Medical Research Council, Hoffmann La Roche, and Maxim Pharmaceuticals.
Funding
This study was supported by the European Community (QLK2-2000-00836), the Swedish Society Against Cancer (Cancerfonden), The Swedish Medical Research Council, Hoffmann La Roche, and Maxim Pharmaceuticals.
Funders | Funder number |
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Maxim Pharmaceuticals | |
Swedish Society Against Cancer | |
Roche | |
European Commission | QLK2-2000-00836 |
Medicinska Forskningsrådet |
Keywords
- Antiviral agents
- Hepatitis C
- Histopathology
- Liver disease
- Liver fibrosis
- Needle biopsy