4.4 Article

Atazanavir is not associated with an increased risk of cardio or cerebrovascular disease events

Journal

AIDS
Volume 27, Issue 3, Pages 407-415

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e32835b2ef1

Keywords

atazanavir; cardiovascular disease; cerebrovascular disease; HIV; myocardial infarction; stroke

Funding

  1. Highly Active Antiretroviral Therapy Oversight Committee (HAART-OC)
  2. European Agency for the Evaluation of Medicinal Products
  3. United States Food and Drug Administration
  4. Abbott Laboratories
  5. Boehringer Ingelheim Pharmaceuticals Inc.
  6. Bristol-Myers Squibb
  7. Gilead Sciences Inc.
  8. Viiv Healthcare
  9. Merck Co Inc.
  10. Pfizer Inc
  11. F. Hoffman-LaRoche Ltd
  12. Janssen Pharmaceuticals
  13. Health Insurance Fund Council, Amstelveen, the Netherlands [CURE/97-46486]
  14. Agence Nationale de Recherches sur le SIDA
  15. U.S. National Institutes of Health's National Institute of Allergy and Infectious Diseases (NIAID) [U01-AI069907]
  16. Merck Sharp Dohme
  17. Gilead Sciences
  18. Roche
  19. Pfizer
  20. GlaxoSmithKline
  21. The Australian Government Department of Health and Ageing
  22. Fondo de Investigacion Sanitaria [FIS 99/0887]
  23. Fundacion para la Investigacion y la Prevencion del SIDA en Espana [FIPSE 3171/00]
  24. National Institute of Allergy and Infectious Diseases, National Institutes of Health [5U01AI042170-10, 5U01AI046362-03]
  25. BIOMED 1 [CT94-1637]
  26. BIOMED 2 [CT97-2713]
  27. European Commission [QLK2-2000-00773]
  28. Pfizer Inc.
  29. Swiss National Science Foundation
  30. Gilead
  31. Boehringer Ingelheim
  32. Janssen-Cilag
  33. Abbott
  34. TRB Chemedica
  35. Tibotec
  36. Johnson Johnson
  37. GSK Bio
  38. Janssen
  39. Bristol-Myer Squibb
  40. Abbott Pharmaceuticals

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Objective: To investigate whether there is any association between exposure to atazanavir (ATV), either when boosted or unboosted by ritonavir, and myocardial infarction (MI) or stroke within the D:A:D: Study. Design: Prospective cohort collaboration. Methods: Poisson regression was used to investigate the association between cumulative exposure to ATV and MI/stroke risk after adjusting for known demographic and clinical confounders, as well as cumulative and recent exposure to specific anti-retroviral drugs. Follow-up started on enrolment in the study and ended at the earliest of: a new MI/stroke event, death, 6 months after last clinic visit, or 1 February 2011. Results: The incidence of MI varied from 0.28 [95% confidence interval (CI) 0.26-0.30)]/100 person-years of follow-up (PYFU) in those with no exposure to ATV to 0.20 (0.12-0.32)/100 PYFU in those with more than 3 years exposure. There was no evidence of an association between cumulative exposure to ATV and MI risk, either in univariate [relative rate/year 0.96 (95% CI 0.88-1.04)] or multivariable [0.95 (0.87-1.05)] analyses. The incidence of stroke was 0.17 (0.16-0.19)/100 PYFU in those with no exposure to ATV and 0.17 (0.10-0.27)/100 PYFU in those with more than 3 years exposure. As with the MI endpoint, there was no evidence of an association with ATV exposure in either univariate [1.02 (0.98-1.05)] or multivariable [0.95 (0.87-1.05)] analyses. Conclusion: These results argue against a class-wide association between exposure to HIV protease inhibitors and the risk of cardio/cerebrovascular events. (C) 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins AIDS 2013, 27:407-415

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