Abstract | BACKGROUND/AIMS: METHODS: Forty-one patients with HBV-related chronic liver disease received randomly either: (a) recombinant alpha 2b interferon (n = 20) 3 MIU, subcutaneously, three times a week for 4 months, or (b) no treatment (n = 21). Patients were followed up for 12 months after completion of therapy. RESULTS: In the interferon-treated group, complete response (loss of HBV- DNA and HBeAg) was significantly higher than spontaneous clearance in the control group (50% vs. 4.8% p < 0.05). Seroconversion to anti-HBe was seen in 35% of the treated and 4.8% of the control group (p < 0.05) at 4 months; it was noticeably higher in patients with chronic hepatitis than in those with cirrhosis. In the responders, alanine aminotransferase levels nearly normalized. One year after interferon therapy, HBeAg and HBV- DNA clearance was observed in 65% of patients, with HBsAg clearance in 15%. Reactivation was not seen in any patient. Side-effects were transient and minimal. CONCLUSION:
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Authors | S K Sarin, R C Guptan, V Thakur, S Malhotra, V Malhotra, K Banerjee, P Khandekar |
Journal | Journal of hepatology
(J Hepatol)
Vol. 24
Issue 4
Pg. 391-6
(Apr 1996)
ISSN: 0168-8278 [Print] Netherlands |
PMID | 8738724
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Interferon alpha-2
- Interferon-alpha
- Recombinant Proteins
- Alanine Transaminase
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Topics |
- Alanine Transaminase
(blood)
- Asia
(ethnology)
- Chronic Disease
- Dose-Response Relationship, Drug
- Follow-Up Studies
- Hepatitis
(therapy)
- Hepatitis B
(complications)
- Humans
- India
(ethnology)
- Interferon alpha-2
- Interferon-alpha
(adverse effects, therapeutic use)
- Liver Cirrhosis
(therapy)
- Liver Diseases
(ethnology, therapy, virology)
- Recombinant Proteins
- Treatment Outcome
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