医学临床研究
醫學臨床研究
의학림상연구
JOURNAL OF CLINICAL RESEARCH
2013年
9期
1690-1691,1692
,共3页
曹春蕊%郄兰霞%黄艳%戴二黑%李新华
曹春蕊%郄蘭霞%黃豔%戴二黑%李新華
조춘예%극란하%황염%대이흑%리신화
肝炎病毒,乙型%拉米夫定/治疗应用
肝炎病毒,乙型%拉米伕定/治療應用
간염병독,을형%랍미부정/치료응용
Hepatitis B virus%Lamivudine/TH
[目的]探讨乙型肝炎病毒(HBV)Bcp/pc 区变异位点与拉米夫定抗病毒治疗后 HBV DNA 反弹的关系。[方法]检测41例拉米夫定治疗(100 mg/d)1年以上,达到病毒学应答半年以上,再出现 HBV DNA 反弹的乙型肝炎患者(反弹组),以及36例拉米夫定治疗 HBV DNA 持续阴性患者(对照组)的 Bcp/pc 区突变位点。[结果]反弹组治疗后 BCP T1762/A1764双突变检出率(75.6%)高于治疗前检出率(48.8%,P =0.023),同时也高于对照组检出率(39.0%,P =0.010)。反弹组41例中 YMDD 变异检出率为63.4%(26/41)。经多因素回归分析发现,YMDD 变异(OR=55.323,P <0.001)、BCPT1762/A1764双突变(OR=10.851,P =0.013)是 HBV DNA 反弹的独立预测因素,而前 C 区 A1896突变与 HBV DNA 反弹无明显关联。[结论]BCPA1762T/G1764A双突变可能与拉米夫定治疗后 HBV DNA 反弹有关。
[目的]探討乙型肝炎病毒(HBV)Bcp/pc 區變異位點與拉米伕定抗病毒治療後 HBV DNA 反彈的關繫。[方法]檢測41例拉米伕定治療(100 mg/d)1年以上,達到病毒學應答半年以上,再齣現 HBV DNA 反彈的乙型肝炎患者(反彈組),以及36例拉米伕定治療 HBV DNA 持續陰性患者(對照組)的 Bcp/pc 區突變位點。[結果]反彈組治療後 BCP T1762/A1764雙突變檢齣率(75.6%)高于治療前檢齣率(48.8%,P =0.023),同時也高于對照組檢齣率(39.0%,P =0.010)。反彈組41例中 YMDD 變異檢齣率為63.4%(26/41)。經多因素迴歸分析髮現,YMDD 變異(OR=55.323,P <0.001)、BCPT1762/A1764雙突變(OR=10.851,P =0.013)是 HBV DNA 反彈的獨立預測因素,而前 C 區 A1896突變與 HBV DNA 反彈無明顯關聯。[結論]BCPA1762T/G1764A雙突變可能與拉米伕定治療後 HBV DNA 反彈有關。
[목적]탐토을형간염병독(HBV)Bcp/pc 구변이위점여랍미부정항병독치료후 HBV DNA 반탄적관계。[방법]검측41례랍미부정치료(100 mg/d)1년이상,체도병독학응답반년이상,재출현 HBV DNA 반탄적을형간염환자(반탄조),이급36례랍미부정치료 HBV DNA 지속음성환자(대조조)적 Bcp/pc 구돌변위점。[결과]반탄조치료후 BCP T1762/A1764쌍돌변검출솔(75.6%)고우치료전검출솔(48.8%,P =0.023),동시야고우대조조검출솔(39.0%,P =0.010)。반탄조41례중 YMDD 변이검출솔위63.4%(26/41)。경다인소회귀분석발현,YMDD 변이(OR=55.323,P <0.001)、BCPT1762/A1764쌍돌변(OR=10.851,P =0.013)시 HBV DNA 반탄적독립예측인소,이전 C 구 A1896돌변여 HBV DNA 반탄무명현관련。[결론]BCPA1762T/G1764A쌍돌변가능여랍미부정치료후 HBV DNA 반탄유관。
[Objective]To explore the relationship between the mutations of hepatitis B virus(HBV)Bcp/pc area and HBVDNA rebound after lamivudine antiviral therapy.[Methods]Mutations of HBV Bcp/pc area of 41 hepatitis B patients with HBVDNA rebound after 100mg/d lamivudine therapy for more than one year and virology response for more than half a year(rebound group)and 36 patients with continuous negative HBVDNA(control group)were detected.[Results]The detection rate of dual mutations of BCP T1762/A1764 in rebound group (75.6%)after treatment was higher than that before treatment(48.8%)(P =0.023),and also higher than that in control group(39.0%)(P =0.010).The detection rate of YMDD mutation in 41 patients of rebound group was 63.4%(26/41).Multivariate regression analysis showed that YMDD mutation(OR= 55.323,P < 0.001)and BCPT1762/A1764 double mutations(OR=10.851,P =0.013)were independent predictive factors of HBVDNA rebound,while A1896 mutation in pre-C area had no obvious correlation with HBVDNA rebound.[Conclusion]BCPA1762T/G1764A double mutants may be associated with HBVDNA rebound after lamivudine treatment.