Randomized controlled trial of adenine arabinoside 5'-monophosphate in chronic active hepatitis B: comparison of the efficacy in heterosexual and homosexual patients
- PMID: 2474480
- DOI: 10.1002/hep.1840100313
Randomized controlled trial of adenine arabinoside 5'-monophosphate in chronic active hepatitis B: comparison of the efficacy in heterosexual and homosexual patients
Abstract
Twenty-two heterosexuals and 21 homosexuals with chronic active hepatitis B and who had HBsAg, HBeAg and hepatitis B virus DNA in serum were randomized separately to receive adenine arabinoside monophosphate or placebo. In the 10 heterosexuals and nine homosexuals who received placebo, no change in hepatitis B virus DNA level and HBeAg was observed. Among the patients who received adenine arabinoside monophosphate, seven of the 12 heterosexuals and five of the 12 homosexuals lost hepatitis B virus DNA; five heterosexuals and three homosexuals also lost HBeAg; one homosexual lost HBsAg. There was no significant differences in response between heterosexual and homosexual patients. When results were pooled, there was a significant effect of adenine arabinoside monophosphate on hepatitis B virus replication. None of the 19 patients who received placebo but 50% of the 24 patients who received adenine arabinoside monophosphate were negative for serum hepatitis B virus DNA at 10 months after treatment (p less than 0.001) and none of the 19 patients who received placebo and 33% of the 24 patients who received adenine arabinoside monophosphate were negative for HBeAg in serum (p less than 0.005). Retrospective analysis showed that disappearance of hepatitis B virus DNA after administration of adenine arabinoside monophosphate was more common (i) in patients with a low pretreatment hepatitis B virus DNA level than in patients with a high pretreatment hepatitis B virus DNA level (8/11 vs. 4/13, p less than 0.05); (ii) in patients with a high pretreatment ALT level than in patients with a low pretreatment ALT level (10/14 vs. 2/10, p less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
Comment in
-
Efficacy and neurotoxicity of ARA-AMP in CAH-B.Hepatology. 1990 Apr;11(4):713. doi: 10.1002/hep.1840110435. Hepatology. 1990. PMID: 1691734 No abstract available.
Similar articles
-
A randomized study of the effects of adenine arabinoside 5'-monophosphate (short or long courses) and lymphoblastoid interferon on hepatitis B virus replication.Hepatology. 1985 Nov-Dec;5(6):1132-8. doi: 10.1002/hep.1840050612. Hepatology. 1985. PMID: 2415436 Clinical Trial.
-
A randomised controlled trial of adenine arabinoside 5'-monophosphate (ARA-AMP) in chronic hepatitis B virus infection.J Hepatol. 1986;3 Suppl 2:S107-10. doi: 10.1016/s0168-8278(86)80107-6. J Hepatol. 1986. PMID: 2439568 Clinical Trial.
-
Therapy of chronic type B hepatitis with adenine arabinoside and adenine arabinoside monophosphate.J Hepatol. 1986;3 Suppl 2:S73-80. doi: 10.1016/s0168-8278(86)80103-9. J Hepatol. 1986. PMID: 2439579 Clinical Trial.
-
A review of the efficacy of adenine arabinoside and lymphoblastoid interferon in the Royal Free Hospital studies of hepatitis B virus carrier treatment: identification of factors influencing response rates.Infection. 1987;15 Suppl 1:S26-31. doi: 10.1007/BF01650108. Infection. 1987. PMID: 2439462 Review.
-
Treatment of the chronic hepatitis B virus carrier state.J Infect. 1988 May;16(3):221-9. doi: 10.1016/s0163-4453(88)97508-1. J Infect. 1988. PMID: 2456355 Review.
Cited by
-
Adenine arabinoside 5'-monophosphate in patients with chronic hepatitis B: comparison of the efficacy in patients with high and low viral replication.Gut. 1995 Mar;36(3):422-6. doi: 10.1136/gut.36.3.422. Gut. 1995. PMID: 7535285 Free PMC article. Clinical Trial.
-
Fatal liver failure caused by reactivation of lamivudine-resistant hepatitis B virus: a case report.World J Gastroenterol. 2007 Feb 14;13(6):964-9. doi: 10.3748/wjg.v13.i6.964. World J Gastroenterol. 2007. PMID: 17352033 Free PMC article.
-
2',3'-dideoxy-beta-L-5-fluorocytidine inhibits duck hepatitis B virus reverse transcription and suppresses viral DNA synthesis in hepatocytes, both in vitro and in vivo.Antimicrob Agents Chemother. 1996 Feb;40(2):448-53. doi: 10.1128/AAC.40.2.448. Antimicrob Agents Chemother. 1996. PMID: 8834896 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical