Prevalence and clinical correlates of YMDD variants during lamivudine therapy for patients with chronic hepatitis B

被引:501
作者
Lai, CL
Dienstag, J
Schiff, E
Leung, NWY
Atkins, M
Hunt, C
Brown, N
Woessner, M
Boehme, R
Condreay, L
机构
[1] Queen Mary Hosp, Univ Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Prince Wales Hosp, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
[3] Massachusetts Gen Hosp, Gastrointestinal Unit, Med Serv, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[5] Univ Miami, Sch Med, Ctr Liver Dis, Miami, FL USA
[6] GlaxoSmithKline, Res Triangle Pk, NC USA
[7] GlaxoSmithKline, Greenford, Middx, England
关键词
D O I
10.1086/368083
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
YMDD variants of hepatitis B virus (HBV) emerge in some patients with chronic hepatitis B who receive lamivudine. YMDD variants were examined in 794 patients in 4 controlled studies of 1 year's duration. The long-term effects of YMDD variants were examined in a subset of patients treated up to 4 years. YMDD variants were detected by polymerase chain reaction (PCR) and restriction fragment-length polymorphism assays. After 1 year, YMDD variants were detected in 81 (24%) of 335 patients. In these patients, the median serum HBV DNA concentration at 1 year was <20% of the baseline level, and serum alanine transaminase (ALT) levels and liver histologic findings had significantly improved. In patients with YMDD variants who were treated for up to 4 years, median HBV DNA and ALT levels showed improvements. Sex, baseline body mass index, and HBV DNA level were associated with emergence of YMDD variants. Patients with YMDD variants losing clinical response with a significant increase in the HBV DNA and ALT levels may require additional therapy.
引用
收藏
页码:687 / 696
页数:10
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