Abstract | AIM: METHODS: Forty-seven consecutive patients with chronic hepatitis B (range 4-16 years, mean 8 years) underwent IFN treatment (3 MU tiw for 20 wk). Fibrosis stage and inflammation grade were assessed in a blinded fashion before and 12 mo after end of treatment. Serum fibrosis markers were determined using automated assays. RESULTS: IFN treatment improved histological inflammation but did not change fibrosis in the whole group or in subgroups. Only hyaluronan correlated significantly with histological fibrosis(r = 0.3383, P = 0.021). Basal fibrosis markers did not differ between responders (42.5%) and nonresponders(57.5%). During IFN treatment only serum tenascin decreased significantly in the whole group and in nonresponders. When pretreatment values were compared to values 12 mo after therapy, TIMP-1 increased in all patients and in nonresponders, and hyaluronan decreased in all patients and in responders. CONCLUSION:
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Authors | Dariusz-Marek Lebensztejn, Maria-Elzbieta Sobaniec-Lotowska, Maciej Kaczmarski, Michael Voelker, Detlef Schuppan |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 12
Issue 21
Pg. 3338-43
(Jun 07 2006)
ISSN: 1007-9327 [Print] United States |
PMID | 16733849
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antiviral Agents
- Biomarkers
- Collagen Type VI
- Extracellular Matrix Proteins
- Interferon-alpha
- Tenascin
- Tissue Inhibitor of Metalloproteinase-1
- Hyaluronic Acid
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Topics |
- Adolescent
- Antiviral Agents
(pharmacology, therapeutic use)
- Biomarkers
(blood)
- Child
- Child, Preschool
- Collagen Type VI
(blood)
- Extracellular Matrix Proteins
(blood)
- Female
- Hepatitis C, Chronic
(blood, drug therapy)
- Humans
- Hyaluronic Acid
(blood)
- Inflammation
- Interferon-alpha
(pharmacology, therapeutic use)
- Liver
(drug effects, pathology)
- Liver Cirrhosis
(blood, pathology)
- Male
- Prospective Studies
- Sensitivity and Specificity
- Tenascin
(blood)
- Tissue Inhibitor of Metalloproteinase-1
(blood)
- Treatment Outcome
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