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超敏实时扩增阻滞突变系统定量PCR法定期检测慢性乙型肝炎患者拉米夫定治疗期间乙肝病毒YVDD突变的临床意义

Clinical significance of periodic detection of hepatitis B virus YVDD mutation by ultrasensitive real-time amplification refractory mutation system quantitative PCR during lamivudine treatment in patients with chronic hepatitis B.

作者信息

Zeng Yongbin, Yang Bin, Wu Yingying, Chen Jing, Shang Hongyan, Chen Xiao, Su Mingkuan, Wu Songhang, Lin Jinpiao, Ou Qishui

机构信息

Department of Gene Diagnosis, Fujian Medical University, Fuzhou, PR China.

Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, PR China.

出版信息

J Med Microbiol. 2015 Mar;64(Pt 3):237-242. doi: 10.1099/jmm.0.000022. Epub 2015 Jan 16.

Abstract

Monitoring hepatitis B virus (HBV) mutants periodically during nucleoside analogue treatment is of great clinical significance, particularly in persistently HBV DNA-positive patients. However, few studies have investigated the dynamic changes of HBV YMDD (Tyr-Met-Asp-Asp) and YVDD (Tyr-Val-Asp-Asp) populations in chronic hepatitis B (CHB) patients whilst undergoing lamivudine (LMV) treatment. In this study, we sought to investigate the dynamic changes of HBV YMDD and YVDD variants by ultrasensitive real-time amplification refractory mutation system quantitative PCR (RT-ARMS-qPCR) and evaluate its significance for changes in the treatment of CHB patients. RT-ARMS-qPCR was established and evaluated with standard recombinant plasmids. Fifteen CHB patients receiving LMV (100 mg daily) were consecutively recruited and followed up for 60 weeks. Serum samples were obtained from each patient at baseline and every 12 weeks. The total HBV DNA, HBV YMDD DNA and YVDD DNA levels were measured using RT-ARMS-qPCR at all given time points after treatment. Routine liver biochemistry parameters, including aspartate aminotransferase and alanine aminotransferase, were also measured every 12 weeks. The linear range of the assay was between 1×10(12) and 1×10(5) copies ml(-1). The low detection limit was 1×10(4) copies ml(-1). After 60 weeks of LMV treatment, nine patients experienced virological breakthrough. The YVDD variant could be detected 12-48 weeks before virological breakthrough. The YVDD variant was detected as the predominant population (range 69.4-100 %) in patients by the time virological breakthrough appeared. We concluded that RT-ARMS-qPCR was sensitive for the detection and quantification of low levels of HBV mutation. Periodic detection of HBV YM(V)DD every 12 weeks during LMV treatment is helpful for therapeutic decision making.

摘要

在核苷类似物治疗期间定期监测乙型肝炎病毒(HBV)突变体具有重要的临床意义,尤其是对于HBV DNA持续阳性的患者。然而,很少有研究调查慢性乙型肝炎(CHB)患者在接受拉米夫定(LMV)治疗时HBV YMDD(酪氨酸-甲硫氨酸-天冬氨酸-天冬氨酸)和YVDD(酪氨酸-缬氨酸-天冬氨酸-天冬氨酸)群体的动态变化。在本研究中,我们试图通过超灵敏实时扩增阻滞突变系统定量PCR(RT-ARMS-qPCR)研究HBV YMDD和YVDD变异体的动态变化,并评估其对CHB患者治疗变化的意义。用标准重组质粒建立并评估RT-ARMS-qPCR。连续招募15例接受LMV(每日100 mg)治疗的CHB患者,并随访60周。在基线时以及每12周从每位患者采集血清样本。在治疗后的所有给定时间点,使用RT-ARMS-qPCR测量总HBV DNA、HBV YMDD DNA和YVDD DNA水平。每12周还测量常规肝脏生化参数,包括天冬氨酸转氨酶和丙氨酸转氨酶。该检测方法的线性范围在1×10(12)至1×10(5)拷贝/毫升之间。最低检测限为1×10(4)拷贝/毫升。LMV治疗60周后,9例患者出现病毒学突破。在病毒学突破前12至48周可检测到YVDD变异体。到病毒学突破出现时,YVDD变异体在患者中被检测为主要群体(范围为69.4-100%)。我们得出结论,RT-ARMS-qPCR对低水平HBV突变的检测和定量很敏感。在LMV治疗期间每12周定期检测HBV YM(V)DD有助于治疗决策。

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