K. Van Vaerenbergh et al., Prevalence of genotypic resistance among antiretroviral drug-naive HTV-1-infected patients in Belgium, ANTIVIR TH, 6(1), 2001, pp. 63-70
Objectives: To estimate the prevalence and the evolution over time (1995-19
98) of genotypic resistance to antiviral drugs in antiretroviral drug-naive
HIV-1-infected patients in Belgium.
Design: Belgian Aids Reference Laboratories provided retrospective samples
and clinical data from antiretroviral drug-naive HIV-l-infected patients wh
o visited the hospital for the first time in 1995 (n=45), 1997 (n=75) and 1
998 (n=111). Genotypic resistance to the three available classes of drugs w
as monitored using the Line Probe Assay (Innogenetics, Gent, Belgium). Addi
tionally, ARMS-151 was performed for scoring multinucleoside resistance.
Results: The prevalence of genotypic resistance at baseline to nucleoside a
nalogue reverse transcriptase inhibitors (NRTls) and non-nucleoside reverse
transcriptase inhibitors (NNRTls) were each between 10% and 20% for 1995,
1997 and 1998 without an increasing trend over time. For NRTls, resistance
mutations were mainly related to zidovudine in 1995, whereas in 1997 and 19
98 baseline resistance was scored for zidovudine, lamivudine or for both dr
ugs simultaneously. No patients displayed the multi-nucleoside resistance Q
151M mutation. Baseline resistance mutations to protease inhibitors (Pls) d
id not rise significantly: 4.4% in 1995, 8% in 1997 and 9.9% in 1998. When
scoring any resistance-related mutation, 26.6% displayed genotypic baseline
resistance in 1995, 26.6% in 1997 and 31.5% in 1998.
Discussion: The prevalence of genotypic baseline resistance to any drug, as
scored with LiPA, in naiveHIV-1 patients in Belgium is 29%, with baseline
resistance mutations to one or several drugs from all available classes of
antiviral drugs. The ability of LiPA to pick up minor variants could be an
explanation for the higher overall prevalence we observe, when compared to
recent estimates in other countries of 16.3% and 22%, which were based on s
equencing methods. According to the European guidelines for resistance test
ing, resistance testing in Belgium before starting antiviral therapy should
be considered.