4.4 Article

Use of nucleoside reverse transcriptase inhibitors and risk of myocardial infarction in HIV-infected patients

Journal

AIDS
Volume 22, Issue 14, Pages F17-F24

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e32830fe35e

Keywords

abacavir; cardiovascular disease; interleukin-6; myocardial infarction

Funding

  1. Medical Research Council [MC_U122886352] Funding Source: Medline
  2. NIAID NIH HHS [U01 AI068641, U01 AI046362-01, U01 AI042170, U01 AI046362-04, U01 AI046362-05S2, U01 AI046362-05S1, U01 AI046362-02, U01 AI046362-03, U01 AI068641-02, U01 AI046362-05, U01 AI068641-03, U01 AI068641-01S1, U01 AI046362-02S1, U01 AI068641-01, U01 AI068641-02S1, U01AI068641, U01AI46362, U01AI042170, U01 AI046362-02S2, U01 AI046362] Funding Source: Medline
  3. Medical Research Council [MC_U122886352] Funding Source: researchfish
  4. MRC [MC_U122886352] Funding Source: UKRI

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Background: Two nucleos(t)ide reverse transcriptase inhibitors (NRTIs) - abacavir and didanosine - may each be associated with excess risk of myocardial infarction. The reproducibility of this finding in an independent dataset was explored and plausible biological mechanisms were sought. Methods: Biomarkers, ischemic changes on the electrocardiogram, and rates of various predefined types of cardiovascular disease (CVD) events according to NRTIs used were explored in the Strategies for Management of Anti-Retroviral Therapy (SMART) study. Patients receiving abacavir and not didanosine were compared with those receiving didanosine, and to those receiving NRTIs other than abacavir or didanosine (other NRTIs). Patients randomly assigned to the continuous antiretroviral therapy arm of SMART were included in all analyses (N=2752); for the study of biomarkers, patients from the antiretroviral therapy interruption arm were also included. Results: Current use of abacavir was associated with an excess risk of CVCVD compared with other NRTIs. Adjusted hazard ratios for clinical myocardial infarction (n=19), major CVD (myocardial infarction, stroke, surgery for coronary artery disease, and CVD death; n = 70), expanded CVD (major CVD plus congestive heart failure, peripheral vascular disease, coronary artery disease requiring drug treatment, and unwitnessed deaths; n = 112) were 4.3 [95% confidence interval (CI): 1.4-13.0], 1.8 (1.0-3.1), and 1.9 (1.3-2.9). At baseline in a subset of patients with biomarker data, high sensitivity-C-reactive protein and interleukin-6 were 27% (P=0.02) and 16% (P=0.02) higher for patients receiving abacavir (N=175) compared with those receiving other NRTIs (N = 500). Didanosine was associated neither with altered risk of CVD nor with altered levels of biomarkers. Conclusion: Abacavir was associated with an increased risk of CVD. The drug may cause vascular inflammation, which may precipitate a CVD event. (C) 2008 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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