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Comparative Performances of HIV-1 RNA Load Assays at Low Viral Load Levels: Results of an International Collaboration
Author(s) -
Luke C. Swenson,
Bryan Cobb,
Anna María Geretti,
P. Richard Harrigan,
Mario Poljak,
Carole SeguinDevaux,
Chris Verhofstede,
Marc Wirden,
Alessandra Amendola,
Jürg Böni,
Thomas Bourlet,
Jon B. Huder,
Jean-Claude Karasi,
Snježana Židovec Lepej,
Maja M. Lunar,
O. Mukabayire,
Rob Schuurman,
Janez Tomažič,
Kristel Van Laethem,
Linos Vandekerckhove,
Annemarie M. J. Wensing
Publication year - 2013
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.02461-13
Subject(s) - concordance , viremia , viral load , virology , taqman , medicine , beagle , human immunodeficiency virus (hiv) , immunology , biology , real time polymerase chain reaction , gene , genetics
Low-level viremia during antiretroviral therapy and its accurate measurement are increasingly relevant. Here, we present an international collaboration of 4,221 paired blood plasma viral load (pVL) results from four commercial assays, emphasizing the data with low pVL. The assays compared were the Abbott RealTime assay, the Roche Amplicor assay, and the Roche TaqMan version 1 and version 2 assays. The correlation between the assays was 0.90 to 0.97. However, at a low pVL, the correlation fell to 0.45 to 0.85. The observed interassay concordance was higher when detectability was defined as 200 copies/ml than when it was defined as 50 copies/ml. A pVL of ∼100 to 125 copies/ml by the TaqMan version 1 and version 2 assays corresponded best to a 50-copies/ml threshold with the Amplicor assay. Correlation and concordance between the viral load assays were lower at a low pVL. Clear guidelines are needed on the clinical significance of low-level viremia.

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