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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Pathological evolution of hepatitis C virus-"Healthy carriers"
Rodolphe Sobesky1, Pascal Lebray, Bertrand Nalpas
1INSERM U785, Centre Hepato-Biliaire, Hopital Paul Brousse, Villejuif, France. rodolphe.sobesky@pbr.aphp.fr
World Journal of Gastroenterology
|July 9, 2008
Summary
Hepatitis C virus (HCV) patients with normal initial liver biopsies showed no fibrosis progression in 66% of cases. Fibrosis progression was linked to elevated alanine-transaminase (ALT) and body mass index (BMI) over 25.
Area of Science:
- Hepatology
- Virology
- Pathology
Background:
- Hepatitis C virus (HCV) infection can lead to liver fibrosis.
- Predicting fibrosis progression in patients with minimal initial liver damage is crucial for management.
Purpose of the Study:
- To identify factors associated with liver fibrosis progression in HCV-infected patients who initially had no significant pathological lesions.
Main Methods:
- Seventy-six untreated HCV patients with normal liver biopsies (Knodell score ≤3) and detectable HCV-RNA underwent two liver biopsies.
- Markers of fibrosis progression were assessed, including necro-inflammation and fibrosis scores, alanine-transaminase (ALT) levels, and body mass index (BMI).
Main Results:
- 66% of patients showed no fibrosis progression over a median follow-up of 4 years.
- Fibrosis progression was significantly associated with elevated ALT levels (P < 0.05), BMI > 25 (P = 0.03), and the time interval between biopsies (P = 0.01).
- A strong correlation was observed between the progression of necro-inflammation and fibrosis (P = 0.003).
Conclusions:
- Liver fibrosis progression is not universal in HCV patients with initially normal liver histology.
- Elevated ALT and a BMI > 25 are significant predictors of fibrosis progression in this cohort.
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