کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3369650 | 1219045 | 2011 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Comparative frequencies of HIV low-level viremia between real-time viral load assays at clinically relevant thresholds Comparative frequencies of HIV low-level viremia between real-time viral load assays at clinically relevant thresholds](/preview/png/3369650.png)
BackgroundThe introduction of new real-time PCR HIV-1 assays with higher sensitivity and broader dynamic range has resulted in detection of low-level viremia (LLV) (≥50 copies/mL) in some patients who previously had undetectable HIV-1 viral load (VL) (<50 copies/mL) with end-point PCR assays. It is therefore important to compare the performance of end-point and newer real-time PCR assays at medically relevant decision points.ObjectivesThe study compared the results obtained with the end-point COBAS® AMPLICOR HIV-1 MONITOR Test, v1.5 to those obtained by three real-time PCR assays COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 Test; the COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 Test, v2.0; and the Abbott RealTime™ HIV-1 test.Study designA total of 391 plasma specimens from HIV-1-infected patients from three US cities were tested with all four assays. The correlation and concordance of results between real-time and end-point PCR assays were calculated.ResultsThere was a consistent and similar proportion (11.8–14.0%) of HIV-1 VL ≥ 50 copies/mL with the three real-time PCR assays for specimens recording <50 copies/mL on the end-point PCR assay. The real-time PCR assays correlated with the end-point PCR assay within generally accepted limits, but consistently quantified higher than the end-point PCR assay between 50 and 200 copies/mL. Discrepancies in results were associated with patient CD4+ cell count and antiviral medication class.ConclusionsThe clinical interpretation of VL results from real-time PCR assays should take into account their higher sensitivity at the lower quantitation range when assessing patients for disease progression and monitoring response to therapy in HIV-1-infected patients, in line with current treatment guidelines.
Journal: Journal of Clinical Virology - Volume 52, Supplement 1, December 2011, Pages S83–S89