4.7 Article

HIV Replication and Immune Status Are Independent Predictors of the Risk of Myocardial Infarction in HIV-Infected Individuals

期刊

CLINICAL INFECTIOUS DISEASES
卷 55, 期 4, 页码 600-607

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OXFORD UNIV PRESS INC
DOI: 10.1093/cid/cis489

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资金

  1. ANRS (French National Agency for Research on AIDS and Viral Hepatitis)
  2. ANRS
  3. INSERM
  4. French Ministry of Health
  5. Boehringer-Ingelheim
  6. Gilead Sciences
  7. Abbott
  8. Bristol-Myers-Squibb
  9. Glaxo-Smith-Kline
  10. Janssen-Cilag
  11. Merck-Sharp Dohme-Chibret
  12. Roche
  13. ViiV Healthcare
  14. Tibotec

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Background. Individuals infected by human immunodeficiency virus (HIV) have a higher risk of cardiovascular disease than the general population. The specific effects of virological and immunological parameters on the risk of myocardial infarction (MI) in HIV-infected individuals are debated. Methods. We conducted a nested case-control study within the French Hospital Database on HIV. Case patients (n = 289) were patients who, between January 2000 and December 2006, had a prospectively recorded and validated first MI. Up to 5 HIV-infected controls (n = 884) matched for age, sex, and clinical center were selected, at random with replacement, among patients with no history of MI. Conditional logistic regression models were used to identify predictors of the risk of MI. Results. Plasma HIV-1 RNA levels >50 copies/mL, a low CD4 T-cell nadir, and a high CD8 T-cell count were independently associated with an increased risk of MI, with respective odds ratios of 1.51 (95% confidence interval, 1.09-2.10), 0.90 (.83-.97) per log(2) unit, and 1.48 (1.01-2.18) for the highest tertile of CD8 T-cell counts (>1150 cells/mm(3)) compared with the lowest (= 760 cells/mm(3)). Conclusions. Independently of cardiovascular risk factors and antiretroviral therapy, HIV replication, a low CD4 T-cell nadir and a high current CD8 T-cell count are associated with an increased risk of MI in HIV-infected individuals. This suggests new paths for interventions to diminish the risk of MI in HIV-infected patients.

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