Fibrosis Progression in Patients With Chronic Hepatitis C Virus Infection
Marija Zeremski1, Rositsa B Dimova2, Jaroslaw Pillardy3
1Division of Gastroenterology and Hepatology, Weill Cornell Medical College.
Insights
Fibrosis progression in hepatitis C virus (HCV) infection varies by stage, with faster advancement in early stages. Patients experiencing alanine aminotransferase (ALT) flares show increased fibrosis progression.
Area of Science:
- Hepatology
- Virology
- Medical Statistics
Background:
- Hepatitis C virus (HCV) infection is a leading cause of chronic liver disease.
- Fibrosis progression in HCV varies significantly among individuals.
- Understanding factors influencing fibrosis progression is crucial for patient management.
Purpose of the Study:
- To investigate factors influencing fibrosis progression in chronic HCV infection.
- To analyze the relationship between fibrosis stage, alanine aminotransferase (ALT) flares, and disease progression.
- To identify specific HCV genotypes associated with increased cirrhosis risk.
Main Methods:
- Retrospective analysis of 936 liver biopsy specimens from 378 HCV-infected patients.
- Logistic regression and multistate Markov modeling used to analyze associations.
- Inclusion criteria: at least two liver biopsies per patient.
Main Results:
- Fibrosis progression was associated with lower initial fibrosis (P < .001) and occurrence of ALT flares (P = .007).
- Highest progression rates observed between fibrosis stages 0 and 1; lowest between stages 2 and 3.
- HCV genotype 3 infection was linked to a higher likelihood of progressing to cirrhosis (P < .001).
Conclusions:
- HCV fibrosis progression is non-linear and stage-dependent.
- Early-stage fibrosis and ALT flares are indicators of accelerated disease progression.
- HCV genotype 3 poses a greater risk for cirrhosis development.
Background:
Fibrosis progression varies markedly in hepatitis C virus (HCV)-infected individuals. We investigated factors that influence fibrosis progression in chronic HCV infection.
Methods:
HCV-infected patients who underwent at least 2 liver biopsies were included in this study. Associations between fibrosis progression and epidemiologic, virologic, and disease-associated factors were analyzed using logistic regression and multistate Markov modeling.
Results:
We analyzed 936 biopsy specimens obtained from 378 individuals. Mean age (±SD) at first biopsy was 48.3 ± 9.3 years, 59.3% of patients were male, 59.9% were white, and 86.7% were infected with HCV genotype 1. Fibrosis progression and cirrhosis occurred in 57.4% and 5.8%, respectively. Fibrosis progression between the first and last biopsies was associated with lower fibrosis in the first biopsy specimen (P < .001) and with the occurrence of at least 1 flare in the alanine aminotransferase (ALT) level (>200 U/L; P = .007). We found the highest fibrosis progression rate between stages 0 and 1 and the lowest between stages 2 and 3. Increased necroinflammation and higher ALT level were associated with faster progression. HCV genotype 3-infected patients were more likely to progress to cirrhosis (P < .001).
Conclusions:
Fibrosis progression in HCV is not linear but varies according to stage, with the highest progression in patients with the lowest fibrosis severity. Patients who experience flares in the ALT level are also more likely to progress.
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