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在初治的、感染HIV-1且接受洛匹那韦/利托那韦或奈非那韦治疗的患者中,依从性与耐药性发展之间的关系。

Relationship between adherence and the development of resistance in antiretroviral-naive, HIV-1-infected patients receiving lopinavir/ritonavir or nelfinavir.

作者信息

King Martin S, Brun Scott C, Kempf Dale J

机构信息

Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, Illinois 60064, USA.

出版信息

J Infect Dis. 2005 Jun 15;191(12):2046-52. doi: 10.1086/430387. Epub 2005 May 12.

Abstract

BACKGROUND

Relationships between adherence to protease inhibitor (PI)-based therapy and resistance development have not been fully characterized.

METHODS

We conducted a double-blind, randomized, controlled study of lopinavir/ritonavir versus nelfinavir, each administered with stavudine and lamivudine, in 653 antiretroviral-naive, human immunodeficiency virus (HIV)-1-infected patients. Relationships between adherence and probability of resistance development were evaluated by local linear regression or logistic regression.

RESULTS

A higher risk of detectable HIV-1 RNA loads after week 24 was associated with lower adherence (odds ratio [OR], 1.08 per 1% decrease in adherence [95% confidence interval {CI}, 1.05-1.10]; P<.001) and nelfinavir use (OR, 2.4 vs. lopinavir/ritonavir [95% CI, 1.6-3.6]; P<.001). Among all nelfinavir-treated patients, a bell-shaped relationship between adherence and the risk of nelfinavir resistance was observed, with a maximum probability of 20% at 85%-90% adherence. No lopinavir resistance was observed. A bell-shaped relationship was also observed for the probability of lamivudine resistance, with a maximum probability of 50% at 75%-80% adherence to nelfinavir and of 15% at 80%-85% adherence to lopinavir/ritonavir.

CONCLUSIONS

Bell-shaped relationships between adherence and resistance were observed. Irrespective of adherence level, the risk of detectable HIV-1 RNA loads or of PI or lamivudine resistance was significantly higher in nelfinavir-treated patients than in lopinavir/ritonavir-treated patients.

摘要

背景

基于蛋白酶抑制剂(PI)的治疗依从性与耐药性发展之间的关系尚未完全明确。

方法

我们对653例未接受过抗逆转录病毒治疗、感染人类免疫缺陷病毒(HIV)-1的患者进行了一项双盲、随机、对照研究,比较洛匹那韦/利托那韦与奈非那韦,二者均与司他夫定和拉米夫定联合使用。通过局部线性回归或逻辑回归评估依从性与耐药性发展概率之间的关系。

结果

第24周后可检测到的HIV-1 RNA载量风险较高与依从性较低(比值比[OR],依从性每降低1%为1.08[95%置信区间{CI},1.05 - 1.10];P <.001)以及使用奈非那韦有关(OR,与洛匹那韦/利托那韦相比为2.4[95% CI,1.6 - 3.6];P <.001)。在所有接受奈非那韦治疗的患者中,观察到依从性与奈非那韦耐药风险之间呈钟形关系,依从性在85% - 90%时耐药概率最高为20%。未观察到洛匹那韦耐药情况。拉米夫定耐药概率也呈钟形关系,接受奈非那韦治疗依从性在75% - 80%时耐药概率最高为50%,接受洛匹那韦/利托那韦治疗依从性在80% - 85%时耐药概率最高为15%。

结论

观察到依从性与耐药性之间呈钟形关系。无论依从性水平如何,接受奈非那韦治疗的患者中可检测到HIV-1 RNA载量或PI或拉米夫定耐药的风险显著高于接受洛匹那韦/利托那韦治疗的患者。

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