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Long-term decrease in serum N-terminal propeptide of type III procollagen in patients with chronic hepatitis C treated with interferon alfa

✍ Scribed by Takeaki Suou; Keiko Hosho; Yukihiro Kishimoto; Yasushi Horie; Hironaka Kawasaki


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
618 KB
Volume
22
Category
Article
ISSN
0270-9139

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✦ Synopsis


To evaluate the effect of interferon alfa (EN-a) on the hepatic extracellular matrix, we investigated the changes in serum N-terminal propeptide of type I11 procollagen during and after 4 months of INF-ru treatment in 178 treated and 45 nontreated patients with chronic hepatitis C. Serum pretreatment levels in nonresponders were significantly higher than those in long-term and short-term responders, but those levels were not different in the latter two groups. Serum propeptide levels decreased significantly during and after IFN-ru therapy in the treated patients, although those levels were unchanged in the nontreated patients. This decrease was sustained for 12 months after IFN-ru was completed not only in long-but also in short-term responders and nonresponders. Serum propeptide levels decreased in those with elevated pretreatment levels, but not in those with normal initial levels, whereas serum transaminase levels decreased similarly in both groups. The changes in serum propeptide levels during and after treatment were more closely correlated with the initial levels compared with those in serum transaminase levels. These results suggested that IFN-ru treatment induces the long-term suppression of active fibrogenesis in chronic hepatitis C independent of antiviral and anti-necroinflammatory effects, thus preventing progression to cirrhosis. (HEPA-TOLOGY 199622~426-431.)

Hepatitis C virus (HCV) is a positive-stranded RNA virus responsible for most non-A, non-B hepatitis. Chronic hepatitis C is rarely spontaneously resolved, and most cases progress to liver cirrhosis and hepatocellular carcinoma.ls2 Treatment with interferon alfa (IFN-a) is effective for decreasing serum alanine aminotransferase (ALT) levels, improving hepatocellular


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