Literature DB >> 16007397

Clinical course of patients with chronic hepatitis B with viral breakthrough during long-term lamivudine treatment.

Tatsuya Ide1, Ryukichi Kumashiro, Reiichiro Kuwahara, Hiroyuki Koga, Yuriko Koga, Teruko Hino, Kazuo Tanaka, Akiko Hisamochi, Kei Ogata, Michio Sata.   

Abstract

BACKGROUND: We evaluated the clinical course of patients with chronic hepatitis B who showed viral breakthrough during long-term lamivudine therapy.
METHODS: We initially studied 141 patients treated with lamivudine for 1 year or more, and 49 patients who showed viral breakthrough were the subjects of this study. Their mean lamivudine administration period was 2.3 +/- 0.9 years.
RESULTS: After viral breakthrough, breakthrough hepatitis occurred in 47 patients (95.9%), but did not occur in the other 2 (4.1%). Four of the 47 patients with breakthrough hepatitis were observed without further treatment, and the alanine transferase (ALT) level was normalized in 2 of them but fluctuated in the other 2. Breakthrough hepatitis was treated by injection of glycyrrhizin or ursodeoxycholic acid administration in 36 of the remaining 43 patients, and by antiviral drug administration in the other 7 (entecavir in 2 patients, adefovir in 2, and interferon in 3). The ALT level was normalized in 5 of the 36 patients treated with glycyrrhizin or ursodeoxycholic acid, but persistently fluctuated in the other 31. In those with normalized ALT after the occurrence of breakthrough hepatitis, the peak ALT level at that point was significantly lower (86 +/- 47 IU/l) than that in the patients without normalization (206 +/- 167 IU/l).
CONCLUSIONS: These results showed that there were a few patients who did not develop breakthrough hepatitis after showing viral breakthrough, and some who showed normalization of the ALT level after the occurrence of breakthrough hepatitis, but in many patients, ALT continuously fluctuated.

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Year:  2005        PMID: 16007397     DOI: 10.1007/s00535-005-1597-9

Source DB:  PubMed          Journal:  J Gastroenterol        ISSN: 0944-1174            Impact factor:   7.527


  19 in total

1.  A case-control study for clinical and molecular biological differences between hepatitis B viruses of genotypes B and C. Japan HBV Genotype Research Group.

Authors:  E Orito; M Mizokami; H Sakugawa; K Michitaka; K Ishikawa; T Ichida; T Okanoue; H Yotsuyanagi; S Iino
Journal:  Hepatology       Date:  2001-01       Impact factor: 17.425

2.  Transcription-mediated amplification is more useful in the follow-up of patients with chronic hepatitis B treated with lamivudine.

Authors:  T Ide; R Kumashiro; T Hino; S Murashima; K Ogata; Y Koga; M Sata
Journal:  Hepatol Res       Date:  2001-09       Impact factor: 4.288

3.  Clinical outcome and virologic profiles of severe hepatitis B exacerbation due to YMDD mutations.

Authors:  Man-Fung Yuen; Takanobu Kato; Masashi Mizokami; Annie On-On Chan; John Chi-Hang Yuen; He-Jun Yuan; Danny Ka-Ho Wong; Siu-Man Sum; Irene Oi-Lin Ng; Sheung-Tat Fan; Ching-Lung Lai
Journal:  J Hepatol       Date:  2003-11       Impact factor: 25.083

4.  Interferon for treatment of breakthrough infection with hepatitis B virus mutants developing during long-term lamivudine therapy.

Authors:  Fumitaka Suzuki; Akihito Tsubota; Norio Akuta; Takashi Someya; Masahiro Kobayashi; Yoshiyuki Suzuki; Satoshi Saitoh; Yasuji Arase; Kenji Ikeda; Yuzo Miyakawa; Hiromitsu Kumada
Journal:  J Gastroenterol       Date:  2002       Impact factor: 7.527

5.  Decreasing fibrogenesis: an immunohistochemical study of paired liver biopsies following lamivudine therapy for chronic hepatitis B.

Authors:  Y O Kweon; Z D Goodman; J L Dienstag; E R Schiff; N A Brown; E Burchardt; R Schoonhoven; D A Brenner; M W Fried; E Burkhardt
Journal:  J Hepatol       Date:  2001-12       Impact factor: 25.083

6.  Acute exacerbation and hepatitis B virus clearance after emergence of YMDD motif mutation during lamivudine therapy.

Authors:  Y F Liaw; R N Chien; C T Yeh; S L Tsai; C M Chu
Journal:  Hepatology       Date:  1999-08       Impact factor: 17.425

7.  Lamivudine as initial treatment for chronic hepatitis B in the United States.

Authors:  J L Dienstag; E R Schiff; T L Wright; R P Perrillo; H W Hann; Z Goodman; L Crowther; L D Condreay; M Woessner; M Rubin; N A Brown
Journal:  N Engl J Med       Date:  1999-10-21       Impact factor: 91.245

Review 8.  Clinical potential of emerging new agents in hepatitis B.

Authors:  G C Farrell
Journal:  Drugs       Date:  2000-10       Impact factor: 9.546

9.  Factors associated with hepatitis B virus DNA breakthrough in patients receiving prolonged lamivudine therapy.

Authors:  M F Yuen; E Sablon; C K Hui; H J Yuan; H Decraemer; C L Lai
Journal:  Hepatology       Date:  2001-10       Impact factor: 17.425

10.  A one-year trial of lamivudine for chronic hepatitis B. Asia Hepatitis Lamivudine Study Group.

Authors:  C L Lai; R N Chien; N W Leung; T T Chang; R Guan; D I Tai; K Y Ng; P C Wu; J C Dent; J Barber; S L Stephenson; D F Gray
Journal:  N Engl J Med       Date:  1998-07-09       Impact factor: 91.245

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  1 in total

Review 1.  Research Progress on the Antiviral Activity of Glycyrrhizin and its Derivatives in Liquorice.

Authors:  Changchao Huan; Yao Xu; Wei Zhang; Tingting Guo; Haochun Pan; Song Gao
Journal:  Front Pharmacol       Date:  2021-07-06       Impact factor: 5.810

  1 in total

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