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抗逆转录病毒治疗后 HIV-1 感染持续低水平病毒血症相关标志物。

Markers associated with persisting low-level viraemia under antiretroviral therapy in HIV-1 infection.

机构信息

AIDS Reference Laboratory, Department of Clinical Chemistry, Microbiology and Immunology, Ghent University, De Pintelaan 185-Blok A, B-9000 Ghent, Belgium.

出版信息

J Antimicrob Chemother. 2014 Apr;69(4):1098-103. doi: 10.1093/jac/dkt484. Epub 2013 Dec 12.

Abstract

OBJECTIVES

To identify host and viral characteristics associated with long-term persisting low-level viraemia (PLLV) under antiretroviral therapy (ART).

PATIENTS AND METHODS

Seventy-one ART-treated patients with long-term PLLV (20-250 copies/mL) and 102 control patients with systematically undetectable viral load (VL) were selected retrospectively from ART-treated patients followed at the Ghent HIV reference centre. Host and viral characteristics were compared using univariate and multivariate analyses.

RESULTS

Higher plasma VL at therapy initiation (OR 3.52; 95% CI 1.86-6.65; P < 0.001), therapy re-initiation after an interruption (OR 3.94; 95% CI 1.70-9.16; P = 0.001), male gender (OR 4.28; 95% CI 1.40-13.00; P = 0.011), a protease inhibitor-based regimen (OR 2.90; 95% CI 1.20-6.97; P = 0.017) and predicted CCR5 co-receptor tropism (OR 2.53; 95% CI 1.05-6.11; P = 0.039) were independently associated with PLLV.

CONCLUSIONS

VL at ART initiation, therapy history, gender, ART regimen and co-receptor tropism were independently associated with PLLV. Gender, therapy history, co-receptor tropism and VL at ART initiation could be valuable predictive markers to identify patients at risk for PLLV.

摘要

目的

确定与抗逆转录病毒治疗(ART)下长期持续低水平病毒血症(PLLV)相关的宿主和病毒特征。

方法

从在根特 HIV 参考中心接受治疗的患者中回顾性选择了 71 名接受 ART 治疗且长期 PLLV(20-250 拷贝/mL)的患者和 102 名系统检测不到病毒载量(VL)的对照患者。使用单变量和多变量分析比较了宿主和病毒特征。

结果

治疗开始时的血浆 VL 较高(OR 3.52;95%CI 1.86-6.65;P < 0.001)、中断后重新开始治疗(OR 3.94;95%CI 1.70-9.16;P = 0.001)、男性(OR 4.28;95%CI 1.40-13.00;P = 0.011)、基于蛋白酶抑制剂的方案(OR 2.90;95%CI 1.20-6.97;P = 0.017)和预测的 CCR5 共受体嗜性(OR 2.53;95%CI 1.05-6.11;P = 0.039)与 PLLV 独立相关。

结论

ART 开始时的 VL、治疗史、性别、ART 方案和共受体嗜性与 PLLV 独立相关。性别、治疗史、共受体嗜性和 ART 开始时的 VL 可能是识别 PLLV 风险患者的有价值的预测标志物。

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