## Abstract It remains unclear whether mutational patterns of the hepatitis B virus (HBV) genome are associated with the development of severe hepatitis after the emergence of tyrosine‐methionine‐aspartate‐aspartate (YMDD) variants during lamivudine treatment. Thirty patients with chronic hepatitis
Correlation of hepatitis B virus load with loss of e antigen and emerging drug-resistant variants during lamivudine therapy
✍ Scribed by Bernhard Zöllner; Peter Schäfer; Heinz-Hubert Feucht; Matthias Schröter; Jörg Petersen; Rainer Laufs
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 105 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0146-6615
- DOI
- 10.1002/jmv.2087
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✦ Synopsis
Abstract
It remains unclear whether sequential assessment of hepatitis B virus (HBV) load during lamivudine therapy can predict the loss of hepatitis B e antigen or emergence of drug‐resistant variants. Therefore, a longitudinal study was carried out in 28 consecutive patients with chronic hepatitis B who started lamivudine therapy for a median of 12 months (range, 6–31). HBV DNA copy numbers were determined at 3‐month intervals. From month 6 onward, HBV viral load below the detection limit of the PCR was predictive of the loss of envelope antigen (P = 0.043). Continuously detectable HBV DNA during the first 12 months of treatment indicated emergence of drug‐resistant variants (P = 0.034). These data suggest that the goal of lamivudine therapy should be complete suppression of serum HBV DNA. J. Med. Virol. 65:659–663, 2001. © 2001 Wiley‐Liss, Inc.
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## Abstract Adefovir dipivoxil (ADV) has demonstrated clinical activity against both wild‐type and lamivudine‐resistant hepatitis B virus (HBV). We analyzed the evolution of viral load and the changes of polymerase and precore/core promoter sequences in lamivudine‐resistant virus during ADV therapy