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 inGastroenterology (New York, N.Y. 1943) Vol. 124; no. 1; p. 97
Main Authors Ghany, Marc G, Kleiner, David E, Alter, Harvey, Doo, Edward, Khokar, Farooq, Promrat, Kittichai, Herion, David, Park, Yoon, Liang, T Jake, Hoofnagle, Jay H
Format Journal Article
LanguageEnglish
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.
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
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  fullname: Herion, David
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  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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PublicationTitle Gastroenterology (New York, N.Y. 1943)
PublicationTitleAlternate Gastroenterology
PublicationYear 2003
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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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StartPage 97
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
URI https://www.ncbi.nlm.nih.gov/pubmed/12512034
Volume 124
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