A prospective study of the evolution of lamivudine resistance mutations in patients with chronic hepatitis B treated with lamivudine

被引:60
作者
Zoulim, F
Poynard, T
Degos, F
Slama, A
El Hasnaoui, A
Blin, P
Mercier, F
Deny, P
Landais, P
Parvaz, P
Trepo, C
机构
[1] INSERM, U271, F-69003 Lyon, France
[2] Hop La Pitie Salpetriere, Hepatogastroenterol Dept, Paris, France
[3] Hop Beaujon, Hepatogastroenterol Dept, Clichy, France
[4] GlaxoSmithKline Lab, Marly Le Roi, France
[5] Icare, Dept Epidemiol, Massy, France
[6] Dept Bordeaux, Dept Pharmacol, Bordeaux, France
[7] Hop Avicenne, Dept Virol, F-93009 Bobigny, France
[8] Hop Necker Enfants Malad, Dept Biostat, Paris, France
[9] CHU Lyon, Virol Lab, Lyon, France
关键词
genotype; hepatitis B virus; polymerase mutation; precore mutation; treatment resistance;
D O I
10.1111/j.1365-2893.2005.00712.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Lamivudine resistance has been described in subjects with chronic hepatitis B infections, associated with mutations in the viral polymerase gene. The objective of this study was to estimate the emergence rate of lamivudine-resistant viral strains and their consequences over a 2-year period. We evaluated 283 lamivudine-naive subjects with chronic hepatitis B. Clinical and virological features were assessed at inclusion and every 6 months thereafter. Viral DNA was characterized using polymerase chain reaction (PCR)-based sequencing. Potential risk factors for the emergence of lamivudine resistance mutations were assessed using logistic regression analysis. The annualized incidence rate for viral polymerase mutations was 22%. The only independent risk factor identified was high viral load, at inclusion. Detectable viral DNA and elevated transaminases were more frequent in subjects harbouring mutant viral strains, and these underwent a lower rate of hepatitis B e seroconversion. All subjects responded favourably to treatment, with no difference in symptoms between the two groups. This prospective cohort study identified lamivudine-resistant mutations emerging in 22% of subjects, yearly, which were apparently not associated with clinical aggravation over the study period.
引用
收藏
页码:278 / 288
页数:11
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