Yen Yi-Hao, Lu Sheng-Nan, Chen Chien-Hung, Wang Jing-Houng, Wu Chun-Mei, Hung Chao-Hung, Tseng Po-Lin, Hu Tsung-Hui, Changchien Chi-Sin, Lee Chuan-Mo
Division of Hepatogastroenterology, Department of Internal Medicine, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Taiwan.
Liver Int. 2007 Dec;27(10):1349-55. doi: 10.1111/j.1478-3231.2007.01609.x.
To elucidate the associations between the changing patterns of hepatitis B e antigen (HBeAg) levels and the emergence of tyrosine-methionine-aspartate-aspartate (YMDD) mutants in HBeAg non-seroconverted patients undergoing lamivudine therapy.
This study analysed 76 HBeAg-positive naïve chronic hepatitis B patients treated with lamivudine. The median duration of therapy was 52 weeks. The YMDD mutants were detected in 35 patients. The changing patterns of HBeAg levels were categorized into three groups: Descending, Descending-Ascending and Fluctuation. HBeAg breakthrough was defined as progressive HBeAg decreasing to <10% of pretreatment levels, followed by increases exceeding 50 S/Co [the ratio of the sample (S) to the cut-off (Co)] above nadir levels.
Of 76 patients, the sensitivity and specificity for predicting YMDD mutants by the Descending-Ascending pattern were 66 and 100% respectively. Of 17 patients with YMDD mutants in the Descending-Ascending group, hepatitis B virus (HBV) DNA first increased, followed by increased HBeAg levels and finally by biochemical breakthrough. The median intervals between virological breakthrough and HBeAg breakthrough, between HBeAg breakthrough and biochemical breakthrough and between virological breakthrough and biochemical breakthrough were 4, 24 and 33 weeks respectively.
Serial HBeAg levels are useful in predicting YMDD mutant emergence in HBeAg non-seroconverted patients during lamivudine therapy.
为阐明接受拉米夫定治疗的乙肝e抗原(HBeAg)未发生血清学转换患者中HBeAg水平变化模式与酪氨酸-甲硫氨酸-天冬氨酸-天冬氨酸(YMDD)变异体出现之间的关联。
本研究分析了76例接受拉米夫定治疗的HBeAg阳性初治慢性乙型肝炎患者。治疗的中位持续时间为52周。在35例患者中检测到YMDD变异体。HBeAg水平的变化模式分为三组:下降型、下降-上升型和波动型。HBeAg突破定义为HBeAg逐渐下降至低于治疗前水平的10%,随后升高超过最低点水平50 S/Co[样本(S)与临界值(Co)之比]。
76例患者中,下降-上升型模式预测YMDD变异体的敏感性和特异性分别为66%和100%。在下降-上升组的17例YMDD变异体患者中,乙肝病毒(HBV)DNA首先升高,随后HBeAg水平升高,最终出现生化突破。病毒学突破与HBeAg突破之间、HBeAg突破与生化突破之间以及病毒学突破与生化突破之间的中位间隔分别为4周、24周和33周。
在拉米夫定治疗期间,连续监测HBeAg水平有助于预测HBeAg未发生血清学转换患者中YMDD变异体的出现。