Tuboi Suely H, Harrison Lee H, Sprinz Eduardo, Albernaz Ricardo K M, Schechter Mauro
Infectious Diseases Epidemiology Research Unit, Graduate School of Public Health and School of Medicine, University of Pittsburgh, PA, USA.
J Acquir Immune Defic Syndr. 2005 Nov 1;40(3):324-8. doi: 10.1097/01.qai.0000182627.28595.01.
To assess predictors of virologic response 6 months after initiation of highly active antiretroviral therapy (HAART) in a cohort of HIV-infected patients in Brazil.
Treatment-naive patients who started HAART between 1996 and 2004 and had information on viral load at 3-9 months were included. Information was collected on demographic characteristics, antiretroviral regimen, adherence, AIDS diagnosis, baseline CD4 cell count, and viral load. Virologic failure (VF) was defined as viral load > or =400 copies/mL at 6 months or death before completion of 6 months of therapy.
Among 454 patients who met the inclusion criteria, VF occurred in 127 (28.0%). In univariate analysis, VF was associated with younger age (median 34 vs. 37 years, P = 0.003), AIDS diagnosis (relative risk [RR] 1.18, P = 0.009), higher baseline viral load (5.34 vs. 5.00, P = 0.0002), lower baseline CD4 cell count (86 vs. 182, P = 0.006), nonadherence (RR 1.39, P < 0.0001), regimen containing 1 single protease inhibitor, as compared with ritonavir-boosted regimens (odds ratio [OR] 8.5, P < 0.0001), and year therapy initiated before 1999 (P < 0.0001). To minimize the systematic effect of therapy indication, we analyzed the subset of 158 patients with CD4 count < or =200 cells/microL who started therapy after 1999. After adjusting for age, education, adherence, regimen, and baseline viral load, nonadherence (OR 8.78, P = 0.02), and fewer years of education (OR 6.05, P = 0.05) remained associated with VF.
A significant improvement was found in virologic suppression over time, consistent with the introduction of nonnucleoside reverse transcriptase inhibitors and ritonavir-boosted regimens into clinical practice. With currently available therapies, compliance and education were shown to be predictors of virologic response, particularly in more immunocompromised patients.
评估巴西一组HIV感染患者开始高效抗逆转录病毒治疗(HAART)6个月后病毒学反应的预测因素。
纳入1996年至2004年间开始HAART且有3至9个月病毒载量信息的初治患者。收集患者的人口统计学特征、抗逆转录病毒治疗方案、依从性、艾滋病诊断、基线CD4细胞计数和病毒载量等信息。病毒学失败(VF)定义为6个月时病毒载量≥400拷贝/mL或在治疗6个月前死亡。
在454例符合纳入标准的患者中,127例(28.0%)发生病毒学失败。单因素分析显示,病毒学失败与年龄较小(中位数34岁对37岁,P = 0.003)、艾滋病诊断(相对危险度[RR]1.18,P = 0.009)、较高的基线病毒载量(5.34对5.00,P = 0.0002)、较低的基线CD4细胞计数(86对182,P = 0.006)、不依从(RR 1.39,P < 0.0001)、与利托那韦增强方案相比含单一蛋白酶抑制剂的治疗方案(优势比[OR]8.5,P < 0.0001)以及1999年前开始治疗的年份(P < 0.0001)有关。为尽量减少治疗指征的系统影响,我们分析了1999年后开始治疗、CD4计数≤200个细胞/微升的158例患者亚组。在对年龄、教育程度、依从性、治疗方案和基线病毒载量进行校正后,不依从(OR 8.78,P = 0.02)和受教育年限较少(OR 6.05,P = 0.05)仍与病毒学失败相关。
随着时间推移,病毒学抑制有显著改善,这与非核苷类逆转录酶抑制剂和利托那韦增强方案引入临床实践一致。就目前可用的治疗方法而言,依从性和教育程度是病毒学反应的预测因素,尤其是在免疫功能较低的患者中。