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Study
Finds PhenoSense Assay More Precise Than the Antivirogram Assay
and Superior at Detecting Resistance to Abacavir, Didanosine and
Stavudine
The
PhenoSense
and the Antivirogram
assays are widely used resistance assays, but prior
to the current study, no one had yet evaluated their sensitivity
and precision. To assess the precision of the Antivirogram and PhenoSense
assays, researchers examined susceptibility results of HIV-1 isolates
lacking drug resistance mutations and containing matching patterns
of drug resistance mutations.
To
assess sensitivity, they determined for each assay the proportion
of isolates with common patterns of matching drug resistance mutations
having reductions in susceptibility greater than those in isolates
without drug resistance mutations.
Results
The
investigators analyzed protease inhibitor (PI) susceptibility results
obtained by the Antivirogram assay for 293 isolates and by the PhenoSense
assay for 300 isolates.
They analyzed
reverse transcriptase (RT) inhibitor susceptibility results obtained
by the Antivirogram assay for 202 isolates and by the PhenoSense
assay for 126 isolates.
For
wild-type and mutant isolates, the median absolute deviance of the
fold resistance of nucleoside RT inhibitor susceptibility results
was significantly lower for the PhenoSense assay than for the Antivirogram
assay.
The
PhenoSense assay was also significantly more likely than the Antivirogram
assay to detect resistance to abacavir
(Ziagen), didanosine
(Videx), and stavudine
(Zerit) in isolates with the common drug resistance
mutations M41L, M184V, and T215Y (+/-L210W).
They
found no significant differences between the 2 assays for detecting
PI
and non
nucleoside RT inhibitor resistance.
The
authors conclude, “The PhenoSense assay is more precise than the
Antivirogram assay and superior at detecting resistance to
abacavir, didanosine, and stavudine.”
03/28/05
Reference
J
Zhang and others. Comparison of the Precision and Sensitivity of the Antivirogram and PhenoSense
HIV Drug Susceptibility Assays. Journal of Acquired Immune Deficiency
Syndromes 38(4): 439-444, April 1, 2005.
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