Clinical features of chronic hepatitis B patients with YMDD mutation after lamivudine therapy

Verfasser / Beitragende:
HOU Wei; LIU Ke-zhou; ZUMBIKA Edward; NI Qin
Ort, Verlag, Jahr:
Institute of Infectious Diseases, First Affiliated Hospital. School of Medcine, Zhejiang University, Hangzhou 310003, China, 2005
Zeitschriftentitel:
Journal of Zhejiang University. B. Science, Jg. 6; H. 12; S. 1182 - 1187
Format:
Journal Article
Online Zugang:
ID: FETCH-wanfang_journals_zjdxxbb_e2005120083

R512.6+2; Objective: To study the clinical features of chronic hepatitis B (CHB) patients with tyrosine-methionine-aspartateaspartate (YMDD) mutation after lamivudine therapy. Methods: This investigation was a retrospective study of 63 CHB patients with YMDD mutation during lamivudine therapy. Clinical data, including period and types of YMDD mutation; hepatitis B virus (HBV) DNA levels and alanine aminotransferase (ALT) levels before and after YMDD mutation were measured. YMDD mutation in the HBV DNA polymerase gene was determined using polymerase chain reaction (PCR) and direct sequencing. HBV DNA quantification was determined using real-time PCR. Relevant serum markers of HBV were measured. The follow-up period was 12 months after YMDD mutation. Results: YMDD mutation occurred 7~44 months (median, 21.5 months) after the start of lamivudine therapy. The majority of the cases (42/63, 66.6%) had YMDD mutants detected between 12 and 24 months. Four types of YMDD mutation were observed in this study, rtL180M/M2

Journal of Zhejiang University. B. Science

Tyrosine-methionine-aspartate-aspartate (YMDD) mutation; Chronic hepatitis B (CHB); Lamivudine