Extract

(See the Major Article by Doyle et al, on pages 724–32).

Antiretroviral therapy prevents human immunodeficiency virus type 1 (HIV-1)–related complications by suppressing viral replication [1]. To forestall virologic rebound and treatment failure, a regimen must reduce the plasma HIV-1 RNA to a threshold below which the virus does not evolve and develop drug resistance. Although this threshold has not been precisely defined, it is probably near the level of quantification for the conventional assays used in the past decade (ie, <50–75 copies/mL), and hence most clinicians have aimed to maintain a viral load that is “undetectable.” This goal can easily be achieved with many modern regimens [2, 3]. Recently, the sensitivity of these assays has improved, resulting in a lower threshold for undetectability. This change has led to a clinical quandary: Should patients who have very low but detectable viremia be considered as having failed therapy?

To address this question, Doyle and colleagues performed an analysis of patients on therapy who had viral loads below 50 copies/mL as measured by the Abbott RealTime HIV-1 assay [4]. The lower limit of quantification of this test is 40 copies/mL; below this threshold, the assay detects HIV-1 RNA, but only qualitative results (detectable or nondetectable) are reported. Given the lack of clarity regarding the significance of these low RNA levels, the treating clinician was informed only that the patient’s viral load was below 50 copies/mL, and, hence, the actual results did not affect the clinician’s decision making. Based on their unreported results, patients were retrospectively divided into 3 groups: those with viral load of 40–49 copies/mL, those with a detectable but unquantifiable viral load (RNApos), and those with an undetectable viral load (RNAneg). Of 1247 patients, 19% had an initial viral load of 40–49 copies/mL, 41% had a detectable but nonquantifiable viral load <40 copies/mL, and 40% had a truly undetectable viral load. Most patients who had viral load between 40–49 copies/mL had only recently achieved virologic suppression (median 0.2 years), whereas those who were RNApos and RNAneg had been suppressed much longer (median 1.3 years and 2.8 years, respectively). Among the subset of patients for whom information was available, those who had a viral load of 40–49 copies/mL were significantly less likely to have perfect adherence, as assessed by pharmacy records, than those in the RNAneg group.

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