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Published on: August 29, 2025
Fibrosis progression in African Americans and Caucasian Americans with chronic hepatitis C
Norah A Terrault1, Kelly Im, Ross Boylan
1Department of Medicine, University of California San Francisco, San Francisco, California 94143-0538, USA. norah.terrault@ucsf.edu
Insights
Liver fibrosis progression in chronic Hepatitis C Virus (HCV) infection appears slow and similar between African Americans and Caucasian Americans. Further research is needed to understand factors influencing fibrosis in HCV patients.
Area of Science:
- Hepatology and viral gastroenterology
- Clinical research on chronic liver disease progression
- Epidemiology of liver fibrosis
Background:
- Previous studies indicated slower liver fibrosis progression in African Americans (AAs) compared to Caucasian Americans (CAs) with chronic Hepatitis C Virus (HCV) infection.
- Understanding racial differences in fibrosis progression is crucial for personalized treatment strategies.
Purpose of the Study:
- To evaluate and compare the rate of liver fibrosis progression between African American and Caucasian American adults with untreated chronic HCV genotype 1 infection.
- To identify factors associated with liver fibrosis progression in this cohort.
Main Methods:
- A multi-state Markov model was employed to analyze fibrosis progression in a cohort of 143 AA and 157 CA adults.
- Duration of infection was imputed for subjects with a history of injection drug use.
- Biopsy adequacy, age at infection, steatosis, ALT level, and necroinflammatory score were considered.
Main Results:
- The distribution of Ishak fibrosis stages was similar between AAs and CAs.
- AAs showed a 10% lower rate of fibrosis progression than CAs, though this difference was not statistically significant (HR, 0.90; 95% CI, 0.72-1.12).
- The estimated median time to cirrhosis was 79 years overall, with variations between racial groups.
Conclusions:
- Liver fibrosis progression rates were slow in the studied cohort.
- There were no substantial differences in fibrosis progression rates observed between African Americans and Caucasian Americans with chronic HCV infection.
Background & Aims:
Prior studies suggest the rate of liver fibrosis progression is slower in African Americans (AAs) than Caucasian Americans (CAs) with chronic HCV infection.
Methods:
With a multi-state Markov model, fibrosis progression was evaluated in a well-characterized cohort of 143 AA and 157 CA adults with untreated chronic HCV genotype 1 infection. In subjects with a history of injection drug use, duration of infection was imputed from a fitted risk model rather than assumed to be the reported first year of use.
Results:
The distribution of Ishak fibrosis stages was 0 (8.7%), 1/2 (55.7%), 3/4 (29.3%), and 5/6 (6.3%) and was similar in AAs and CAs (P = .22). After adjusting for biopsy adequacy, AAs had a 10% lower rate of fibrosis progression than did CAs, but the difference was not statistically significant (hazard ratio, 0.90; 95% confidence interval, 0.72-1.12). The overall 20-year estimates of probabilities of progression from stage 0 to stages 1/2, 3/4, and 5/6 were 59.3%, 28.8%, and 4.7%, respectively. The estimated median time from no fibrosis to cirrhosis was 79 years for the entire cohort and 74 and 83 years for CAs and AAs, respectively. In 3-variable models including race and biopsy adequacy, the factors significantly associated with fibrosis progression were age when infected, steatosis, ALT level, and necroinflammatory score.
Conclusions:
The rates of fibrosis progression were slow and did not appear to differ substantially between AAs and CAs.
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