Progression of fibrosis in chronic hepatitis C
Fibrosis is the hallmark of hepatic cirrhosis, worsening of which is probably the best surrogate marker for progression of chronic liver disease. We evaluated a large cohort of patients with chronic hepatitis C (CHC) using liver histology to assess the rate and predictors of progression of fibrosis....
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Published in | Gastroenterology (New York, N.Y. 1943) Vol. 124; no. 1; p. 97 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.01.2003
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Abstract | Fibrosis is the hallmark of hepatic cirrhosis, worsening of which is probably the best surrogate marker for progression of chronic liver disease. We evaluated a large cohort of patients with chronic hepatitis C (CHC) using liver histology to assess the rate and predictors of progression of fibrosis.
The cohort consisted of 123 patients with CHC who underwent 2 liver biopsies 4-212 months (mean, 44 months) apart without intervening treatment. Liver histology was graded using the histology activity index (score, 0-18) and fibrosis staged using a scoring system of 0 (no fibrosis) to 6 (cirrhosis).
Among 123 patients, 48 (39%) showed progression in fibrosis scores, 46 (37%) showed no change, and 29 (24%) showed improvement. Of those with worsening fibrosis, 75% had a 1-point increase and 25% a 2-point or greater increase in scores, and 9% showed progression to cirrhosis. The overall rate of progression was 0.12 fibrosis units per year, a rate that predicts progression to cirrhosis in 50 years if progression was linear. The rate of fibrosis progression was variable, and it was higher among older patients, those with higher serum alanine and aspartate aminotransferase levels, and those with the most extensive periportal necrosis on initial liver biopsy.
The best predictors of fibrosis progression in CHC are the extent of serum aminotransferase elevations and the degree of hepatocellular necrosis and inflammation on liver biopsy. These findings support the recommendation that patients with normal aminotransferase levels and mild liver histology can safely defer treatment. |
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AbstractList | Fibrosis is the hallmark of hepatic cirrhosis, worsening of which is probably the best surrogate marker for progression of chronic liver disease. We evaluated a large cohort of patients with chronic hepatitis C (CHC) using liver histology to assess the rate and predictors of progression of fibrosis.
The cohort consisted of 123 patients with CHC who underwent 2 liver biopsies 4-212 months (mean, 44 months) apart without intervening treatment. Liver histology was graded using the histology activity index (score, 0-18) and fibrosis staged using a scoring system of 0 (no fibrosis) to 6 (cirrhosis).
Among 123 patients, 48 (39%) showed progression in fibrosis scores, 46 (37%) showed no change, and 29 (24%) showed improvement. Of those with worsening fibrosis, 75% had a 1-point increase and 25% a 2-point or greater increase in scores, and 9% showed progression to cirrhosis. The overall rate of progression was 0.12 fibrosis units per year, a rate that predicts progression to cirrhosis in 50 years if progression was linear. The rate of fibrosis progression was variable, and it was higher among older patients, those with higher serum alanine and aspartate aminotransferase levels, and those with the most extensive periportal necrosis on initial liver biopsy.
The best predictors of fibrosis progression in CHC are the extent of serum aminotransferase elevations and the degree of hepatocellular necrosis and inflammation on liver biopsy. These findings support the recommendation that patients with normal aminotransferase levels and mild liver histology can safely defer treatment. |
Author | Promrat, Kittichai Herion, David Khokar, Farooq Hoofnagle, Jay H Alter, Harvey Liang, T Jake Ghany, Marc G Doo, Edward Park, Yoon Kleiner, David E |
Author_xml | – sequence: 1 givenname: Marc G surname: Ghany fullname: Ghany, Marc G email: marcg@bdg10.niddk.nih.gov organization: Liver Diseases Section, Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases/NIH, Building 10, Room 9B-06, 10 Center Drive, MSC 1800, Bethesda, MD 20892-1800, USA. marcg@bdg10.niddk.nih.gov – sequence: 2 givenname: David E surname: Kleiner fullname: Kleiner, David E – sequence: 3 givenname: Harvey surname: Alter fullname: Alter, Harvey – sequence: 4 givenname: Edward surname: Doo fullname: Doo, Edward – sequence: 5 givenname: Farooq surname: Khokar fullname: Khokar, Farooq – sequence: 6 givenname: Kittichai surname: Promrat fullname: Promrat, Kittichai – sequence: 7 givenname: David surname: Herion fullname: Herion, David – sequence: 8 givenname: Yoon surname: Park fullname: Park, Yoon – sequence: 9 givenname: T Jake surname: Liang fullname: Liang, T Jake – sequence: 10 givenname: Jay H surname: Hoofnagle fullname: Hoofnagle, Jay H |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/12512034$$D View this record in MEDLINE/PubMed |
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Snippet | Fibrosis is the hallmark of hepatic cirrhosis, worsening of which is probably the best surrogate marker for progression of chronic liver disease. We evaluated... |
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SubjectTerms | Adult Aged Alanine Transaminase - blood Biopsy Disease Progression Female Follow-Up Studies Hepatitis C, Chronic - complications Humans Liver - pathology Liver Cirrhosis - blood Liver Cirrhosis - pathology Liver Cirrhosis - virology Male Middle Aged Time Factors |
Title | Progression of fibrosis in chronic hepatitis C |
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