Elsevier

Journal of Hepatology

Volume 32, Issue 3, March 2000, Pages 447-452
Journal of Hepatology

Prognostic value of serum hyaluronan in patients with compensated HCV cirrhosis

https://doi.org/10.1016/S0168-8278(00)80396-7Get rights and content

Abstract

Background/Aim: Serum hyaluronan (HA) levels increase according to the degree of liver fibrosis in patients with chronic viral hepatitis C. Patients with liver disease and markedly high serum HA levels have cirrhosis with typical signs of hepatic sinusoidal capillarization, a factor of aggravation of cirrhosis. The aim of this study was to evaluate the prognostic value of serum HA for severe complications in asymptomatic patients with HCV cirrhosis.

Methods: Six hundred and sixty-eight patients with anti-HCV antibodies and increased serum alanine aminotransferase were referred to our hospital for evaluation, including liver biopsy. At entry, serum HA levels were measured in 91 patients (64 men, 27 women, 56±11 years old) out of 103 who had asymptomatic, biopsy-proven cirrhosis. According to the criteria of Child-Pugh, 82 were classified A and 9 B. The follow-up period was 6 to 82 months (median: 38 months), and 51 of these patients received alphainterferon therapy during the first year. Severe complications were defined as death or liver transplantation, ascites, bleeding from esophageal varices, encephalopathy, or hepatocellular carcinoma.

Results: Serum HA levels at entry were higher in the cirrhotic patients in whom severe complications occurred during the follow-up period (520±426 μg/l vs. 197±146 μg/l, p<0.0001). The patients with serum hyaluronan levels >350 μg/l displayed higher probabilities of occurrence of severe complications (p<0.0001). Other factors associated with the occurrence of complications or death were: serum bilirubin >18 μmol/l (p=0.03), platelet count <112⨯109/l (p=0.02), prothrombin time <63% (p<0.0001), serum albumin <36 g/l (p=0.002), alkaline phosphatase >81 IU/l (p=0.01), and no interferon treatment (p=0.0003). Multivariate analysis identified five independent factors predictive of severe clinical complications, namely: hyaluronan (p=0.006), prothrombin time (p=0.04), bilirubin (p=0.04), albumin (p=0.04), and no therapy (p=0.03).

Conclusion: Serum HA level is predictive for occurrence of severe complications in HCV cirrhosis, and can be used as a prognostic marker, in addition to the parameters of the Child-Pugh score, particularly in patients with compensated cirrhosis.

Section snippets

Patients

Between December 1989 and December 1994, a total of 668 patients with anti-HCV antibodies and persistently increased serum ALT were primarily referred to our department for evaluation, including liver biopsy. Among these patients, 103 had biopsy-proven cirrhosis with no history or clinical sign of complication.

At entry, serum hyaluronan levels, included in the biological evaluation since October 1990, were measured in 91 of these asymptomatic cirrhotic patients (64 men, 27 women, 56±11 years

Follow-up of the patients

The follow-up period was 38±18 months (median: 38 months). During this follow-up period severe complications occurred in 24 patients (26.4%), including decompensation in 24 and hepatocellular carcinoma in 10 (four decompensated before HCC occurrence). Among them, 14 patients died and three patients had transplantation for liver failure. After interferon therapy, four of the treated patients had normal ALT, and two were serum HCV-RNA negative.

Serum hyaluronan levels

Serum hyaluronan levels were higher in cirrhotic

Discussion

Assessment of the risk of severe complications in patients with cirrhosis has important clinical and therapeutical implications. The most widely used prognostic evaluation of cirrhotic patients is based on the Child-Pugh classification 22., 23.. However this clinically relevant method includes parameters such as ascites or encephalopathy, which are clinical complications of cirrhosis, so that patients with no history or clinical sign of complication, particularly those classified as Child A,

Acknowledgements

This study was presented in part at the 47th AASLD Meeting, Chicago, Illinois, November 8–12, 1996 and published in abstract form (Hepatology 1996; 24: 393A).

References (28)

  • AM Gressner et al.

    Cellular sources of noncollagenous matrix proteins: role of fat-storing cells in fibrogenesis

    Semin Liver Dis

    (1990)
  • JRE Fraser et al.

    Uptake of circulating hyaluronic acid by the rat liver. Cellular localization in situ

    Cell Tissue Res

    (1985)
  • A Engström-Laurent et al.

    Increased serum levels of hyaluronate in liver disease

    Hepatology

    (1985)
  • T Frébourg et al.

    Serum hyaluronate in liver diseases: study by enzymoimmunological assay

    Hepatology

    (1986)
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