Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
PLoS One. 2013 Oct 16;8(10):e77691. doi: 10.1371/journal.pone.0077691. eCollection 2013.
Non-adherence is one of the strongest predictors of therapeutic failure in HIV-positive patients. Virologic failure with subsequent emergence of resistance reduces future treatment options and long-term clinical success.
Prospective observational cohort study including patients starting new class of antiretroviral therapy (ART) between 2003 and 2010. Participants were naïve to ART class and completed ≥1 adherence questionnaire prior to resistance testing. Outcomes were development of any IAS-USA, class-specific, or M184V mutations. Associations between adherence and resistance were estimated using logistic regression models stratified by ART class.
Of 314 included individuals, 162 started NNRTI and 152 a PI/r regimen. Adherence was similar between groups with 85% reporting adherence ≥95%. Number of new mutations increased with increasing non-adherence. In NNRTI group, multivariable models indicated a significant linear association in odds of developing IAS-USA (odds ratio (OR) 1.66, 95% confidence interval (CI): 1.04-2.67) or class-specific (OR 1.65, 95% CI: 1.00-2.70) mutations. Levels of drug resistance were considerably lower in PI/r group and adherence was only significantly associated with M184V mutations (OR 8.38, 95% CI: 1.26-55.70). Adherence was significantly associated with HIV RNA in PI/r but not NNRTI regimens.
Therapies containing PI/r appear more forgiving to incomplete adherence compared with NNRTI regimens, which allow higher levels of resistance, even with adherence above 95%. However, in failing PI/r regimens good adherence may prevent accumulation of further resistance mutations and therefore help to preserve future drug options. In contrast, adherence levels have little impact on NNRTI treatments once the first mutations have emerged.
不依从是 HIV 阳性患者治疗失败的最强预测因素之一。病毒学失败后出现耐药性会降低未来的治疗选择和长期临床疗效。
这是一项包括 2003 年至 2010 年期间开始使用新的抗逆转录病毒治疗(ART)类别的患者的前瞻性观察队列研究。参与者对 ART 类别均无耐药性,且在耐药性检测前完成了至少一份依从性调查问卷。研究终点为出现任何 IAS-USA、类别特异性或 M184V 突变。使用逻辑回归模型,根据 ART 类别分层,评估依从性与耐药性之间的相关性。
在 314 名纳入的个体中,162 名开始使用 NNRTI,152 名开始使用 PI/r 方案。两组的依从性相似,有 85%的人报告依从性≥95%。新突变的数量随不依从性的增加而增加。在 NNRTI 组中,多变量模型表明,发生 IAS-USA(比值比(OR)1.66,95%置信区间(CI):1.04-2.67)或类别特异性(OR 1.65,95%CI:1.00-2.70)突变的可能性呈显著线性关联。PI/r 组中的耐药水平明显较低,且依从性仅与 M184V 突变显著相关(OR 8.38,95%CI:1.26-55.70)。在 PI/r 方案中,依从性与 HIV RNA 显著相关,但在 NNRTI 方案中无显著相关性。
与 NNRTI 方案相比,含 PI/r 的治疗方案对不完全依从性的容忍度更高,即使依从性高于 95%,也允许更高水平的耐药性。然而,在失败的 PI/r 方案中,良好的依从性可能有助于防止进一步耐药突变的积累,从而有助于保留未来的药物选择。相比之下,一旦出现第一种突变,依从性对 NNRTI 治疗的影响就很小。