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在人类免疫缺陷病毒感染患者中,表型药物敏感性检测比治疗史更能预测长期病毒学抑制情况。

Phenotypic drug susceptibility testing predicts long-term virologic suppression better than treatment history in patients with human immunodeficiency virus infection.

作者信息

Call S A, Saag M S, Westfall A O, Raper J L, Pham S V, Tolson J M, Hellmann N S, Cloud G A, Johnson V A

机构信息

Division of General Internal Medicine and Birmingham Veterans Affairs Medical Center, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294-0006, USA.

出版信息

J Infect Dis. 2001 Feb 1;183(3):401-8. doi: 10.1086/318078. Epub 2000 Dec 29.

Abstract

To assess the value of phenotypic drug susceptibility testing as a predictor of antiretroviral treatment response in human immunodeficiency virus (HIV)-infected people, drug susceptibility testing was performed retrospectively on plasma samples collected at baseline in a cohort of 86 antiretroviral-experienced, HIV-infected people experiencing treatment failure and initiating a new antiretroviral treatment regimen. Two separate criteria for reduced drug susceptibility were evaluated. In multivariate analyses, phenotypic susceptibility was an independent predictor of time to treatment failure (adjusted hazards ratio [HR], 0.70; 95% confidence interval [CI], 0.55-0.90; and adjusted HR, 0.76; 95% CI, 0.61-0.95, with reduced drug susceptibility cutoffs defined as 4.0-fold and 2.5-fold higher than reference virus IC(50) values, respectively). Previous protease inhibitor experience was also a significant independent predictor. Notably, drug susceptibility predicted on the basis of treatment history alone was not predictive of time to treatment failure. In this cohort, phenotypic testing results enhanced the ability to predict sustained long-term suppression of virus load.

摘要

为评估表型药物敏感性检测作为人类免疫缺陷病毒(HIV)感染者抗逆转录病毒治疗反应预测指标的价值,对一组86例有抗逆转录病毒治疗经验、出现治疗失败且开始新抗逆转录病毒治疗方案的HIV感染者基线时采集的血浆样本进行了回顾性药物敏感性检测。评估了两种不同的药物敏感性降低标准。在多变量分析中,表型敏感性是治疗失败时间的独立预测指标(调整后风险比[HR]为0.70;95%置信区间[CI]为0.55 - 0.90;调整后HR为0.76;95%CI为0.61 - 0.95,药物敏感性降低阈值分别定义为比参考病毒IC(50)值高4.0倍和2.5倍)。既往蛋白酶抑制剂治疗经历也是一个显著的独立预测指标。值得注意的是,仅基于治疗史预测的药物敏感性并不能预测治疗失败时间。在该队列中,表型检测结果增强了预测病毒载量长期持续抑制的能力。

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