Long-term benefit of genotypic-guided therapy and prevalence of multinucleoside resistance in an Italian group of antiretroviral multiexperienced patients
E. Quiros-roldan et al., Long-term benefit of genotypic-guided therapy and prevalence of multinucleoside resistance in an Italian group of antiretroviral multiexperienced patients, J CL LAB AN, 15(3), 2001, pp. 127-130
Multiple nucleoside resistance involves specific genetic changes in the HIV
-1 reverse transcriptase gene, such as Q151M mutation and an insertion of t
wo serine aminoacids at RT codon 69. Among 432 patients failing antiretrovi
ral therapy, five (1.15%) harboured viruses with Q151M mutation into the RT
gene and no viruses were identified harbouring insertion at codon 69. Also
we have studied the long-term benefit of HIV genotypic testing with the fa
ilure to reach a viral load below 50 copies/ml within 1 year of antiretrovi
ral therapy using as the primary end-point. A group of 64 HIV-positive anti
retroviral multiexperienced patients were examined, all of them failing the
currentART. HIV-RNA changed -0.8 log at month 4 and +0.1 log and -0.5 log
at months 8 and 12, respectively. The proportion of patients with viral loa
d below 50 copies/ml was 19.3,32.8, and 28.1% at months 4, 3, and 12, respe
ctively. In multidrug-experienced patients, genotype-guided therapy is not
in fact able to achieve complete viral suppression in more than 30% of pati
ents after 1 year of ART. The development of more precise resistance tests
and interpretations are needed for better control of HIV replication. Other
metabolic/pharmacokinetics factors of poor drug adherence should also be a
ssessed. J. Clin. Lab. Anal. 15:127-130, 2001. (C) 2001 Wiley-Liss, Inc.