4.4 Article

Relationship between minority nonnucleoside reverse transcriptase inhibitor resistance mutations, adherence, and the risk of virologic failure

期刊

AIDS
卷 26, 期 2, 页码 185-192

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e32834e9d7d

关键词

antiretroviral therapy; HIV-1 drug resistance; medication adherence; minority variants; virologic failure

资金

  1. Bristol-Myers Squibb
  2. Pfizer
  3. Merck
  4. Roche Diagnostics
  5. IrsiCaixa AIDS Research Institute
  6. Lluita contra la SIDA Foundation
  7. ViiV Healthcare
  8. Siemens
  9. Boehringer Ingelheim
  10. Gilead
  11. Abbott
  12. ViiV
  13. Stanford University
  14. Avexa
  15. Boehringer-Ingelheim
  16. GlaxoSmithKline
  17. Oncolys
  18. Roche
  19. Tobira
  20. Vertex
  21. ViroStatistics
  22. Clinical Investigator Training Program
  23. Harvard/MIT Health Sciences and Technology - Beth Israel Deaconess Medical Center
  24. Pfizer Inc.
  25. Merck Co.
  26. CHAIN
  27. Collaborative HIV
  28. Anti-HIV Drug Resistance Network [223131]
  29. European Commission
  30. NIH (Statistical and Data Management Center of the AIDS Clinical Trials Group) [U01 AI068634]
  31. Harvard University CFAR [P30 AI060354]
  32. VA
  33. NIH [U01 AI042170, U01 AI 068636, K24 RR016482]
  34. ACTG

向作者/读者索取更多资源

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-naive 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. (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins

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