Prediction of progressive liver fibrosis in hepatitis C infection by serum and tissue levels of transforming growth factor‐β

• DOI: 10.1046/j.1365-2893.2001.00314.x
• Publication Date: 2003-03-12T09:19:27Z
• Authors: S. Kanzler; M. Baumann; P. Schirmacher; V. Dries; E. Bayer; G. Gerken; H.‐P. Dienes; A. W. Lohse
• Keywords: Liver Cirrhosis; Male; 0301 basic medicine; Alanine Transaminase; Hepatitis C, Chronic; Middle Aged; Viral Load; Antiviral Agents; Severity of Illness Index; 3. Good health; 03 medical and health sciences; Predictive Value of Tests; Transforming Growth Factor beta; Chronic Disease; Disease Progression; Humans; Female; Biomarkers; Procollagen

Although many patients with chronic viral hepatitis C infection suffer from progressive liver disease, the rate of fibrosis progression is highly variable and some patients do not show any measurable progression. However, our ability to predict which patients progress is very limited. Since transforming growth factor‐β (TGF‐β) is a key mediator of liver fibrogenesis, we assessed the predictive role of TGF‐β for fibrogenesis in chronic hepatitis C. We studied 39 patients with chronic hepatitis C in whom two liver biopsies were taken at least 12 months apart, and who did not receive therapy during this period. TGF‐β was measured by bioassay and by ELISA in serum samples taken at the time of the first biopsies, and TGF‐β was determined semiquantitatively by immunostaining of liver biopsy sections. Fibrosis was scored blinded in the biopsy samples by two pathologists independently. There was a close correlation between TGF‐β serum levels and the rate of fibrosis progression. Patients with no progression of fibrosis had significantly lower (59 ng/mL ± 22) TGF‐β serum levels than patients with progressive disease (115 ng/mL ± 20), and a TGF‐β level below 75 ng/mL was predictive for stable disease. Immunohistology for TGF‐β in biopsy samples was also predictive for progressive liver disease with fibrosis progression found in those patients displaying staining of hepatocytes and sinusoidal cells. No such correlation was found with other markers such as procollagen III peptide, viral load or transaminase levels. These results further support the role of TGF‐β in liver fibrogenesis, and offer an opportunity to predict clinical disease progression, which may help in selecting patients who are in need of therapeutic interventions.