TY - JOUR
T1 - Relationship between minority nonnucleoside reverse transcriptase inhibitor resistance mutations, adherence, and the risk of virologic failure
AU - Li, Jonathan Z.
AU - Paredes, Roger
AU - Ribaudo, Heather J.
AU - Svarovskaia, Evguenia S.
AU - Kozal, Michael J.
AU - Hullsiek, Katherine H.
AU - Miller, Michael D.
AU - Bangsberg, David R.
AU - Kuritzkes, Daniel R.
PY - 2012/1/14
Y1 - 2012/1/14
N2 - Objectives: To evaluate the risk of virologic failure conferred by suboptimal adherence to nonnucleoside reverse transcriptase inhibitors (NNRTIs) and minority NNRTI resistance mutations. Design: Pooled analysis of the risk of virologic failure conferred by minority NNRTI resistance mutations and NNRTI adherence from three studies of treatment-naïve individuals initiating an NNRTI-based regimen. Methods: Participants from each study were categorized into both adherence quartiles (Q1-Q4) and four strata: at least 95%, 80-94%, 60-79%, and below 60%. Weighted Cox proportional hazard models were used to estimate the risk of virologic failure. Results: The majority of participants (N=768) had high measured adherence, but those in the lowest adherence quartile had the highest proportion of participants with virologic failure and the risk of virologic failure increased step-wise with adherence below 95%. Detection of minority NNRTI drug resistance mutations increased the proportion of participants with virologic failure across adherence quartiles (Cochran-Mantel-Haenszel P<0.001) and adherence strata [Cochran-Mantel- Haenszel P<0.001; <60% adherence, hazard ratio 1.7 (1.1-2.7), P=0.02; 60- 79% adherence, hazard ratio 1.2 (0.5-3.2), P=0.67; 80-94% adherence, hazard ratio 2.5 (0.98-6.3), P=0.06; ≥95% adherence, hazard ratio 3.6 (2.3-5.6), P<0.001]. On multivariate analysis, the effect of minority variants was also most prominent at higher levels of medication adherence. Conclusions: The presence of minority NNRTI resistance mutations and NNRTI adherence were found to be independent predictors of virologic failure, but also modify each other's effects on virologic failure. In addition to the focus on medication adherence counseling, ultrasensitive HIV-1 drug resistance assays could play a role in optimizing the success rates of first-line antiretroviral therapy.
AB - Objectives: To evaluate the risk of virologic failure conferred by suboptimal adherence to nonnucleoside reverse transcriptase inhibitors (NNRTIs) and minority NNRTI resistance mutations. Design: Pooled analysis of the risk of virologic failure conferred by minority NNRTI resistance mutations and NNRTI adherence from three studies of treatment-naïve individuals initiating an NNRTI-based regimen. Methods: Participants from each study were categorized into both adherence quartiles (Q1-Q4) and four strata: at least 95%, 80-94%, 60-79%, and below 60%. Weighted Cox proportional hazard models were used to estimate the risk of virologic failure. Results: The majority of participants (N=768) had high measured adherence, but those in the lowest adherence quartile had the highest proportion of participants with virologic failure and the risk of virologic failure increased step-wise with adherence below 95%. Detection of minority NNRTI drug resistance mutations increased the proportion of participants with virologic failure across adherence quartiles (Cochran-Mantel-Haenszel P<0.001) and adherence strata [Cochran-Mantel- Haenszel P<0.001; <60% adherence, hazard ratio 1.7 (1.1-2.7), P=0.02; 60- 79% adherence, hazard ratio 1.2 (0.5-3.2), P=0.67; 80-94% adherence, hazard ratio 2.5 (0.98-6.3), P=0.06; ≥95% adherence, hazard ratio 3.6 (2.3-5.6), P<0.001]. On multivariate analysis, the effect of minority variants was also most prominent at higher levels of medication adherence. Conclusions: The presence of minority NNRTI resistance mutations and NNRTI adherence were found to be independent predictors of virologic failure, but also modify each other's effects on virologic failure. In addition to the focus on medication adherence counseling, ultrasensitive HIV-1 drug resistance assays could play a role in optimizing the success rates of first-line antiretroviral therapy.
KW - Antiretroviral therapy
KW - HIV-1 drug resistance
KW - Medication adherence
KW - Minority variants
KW - Virologic failure
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U2 - 10.1097/QAD.0b013e32834e9d7d
DO - 10.1097/QAD.0b013e32834e9d7d
M3 - Article
C2 - 22179227
AN - SCOPUS:84155169026
SN - 0269-9370
VL - 26
SP - 185
EP - 192
JO - AIDS
JF - AIDS
IS - 2
ER -