If patients with human immunodeficiency virus (HIV) infection are already at risk for cardiovascular disease, clinicians are advised to double-check the antiretroviral medication. Researchers from the University of Washington in Seattle discovered a two-fold increase in the risk of elevated blood pressure (BP) among patients receiving lopinavir/ritonavir (Kaletra, Abbott), compared with efavirenz (Sustiva medication, Bristol-Myers Squibb).
Of 444 patients, 83 experienced elevated systolic BP, 33 had elevated dia-stolic BP, and 11 had newly diagnosed hypertension after starting highly active antiretroviral therapy (HAART). Patients taking atazanavir sulfate (Reyataz, Bristol-Myers Squibb), efavirenz, generic nelfinavir mesylate (Viracept tablet, Agouron) and indinavir sulfate (Generic Crixivan, Merck) had significantly lower risk of high BP compared with patients taking lopinavir/ritonavir drug.
Their results suggest that different protease inhibitors influence BP through different mechanisms. For instance, the increased risk associated with lopin-avir/ritonavir was related in part, the researchers say, to an increase in body mass index (BMI). Patients receiving atazanavir-based regimens were at a lower risk for elevated BP compared with those receiving generic efavirenz or lopinavir/ ritonavir even after the researchers adjusted for changes in BMI.
Patients taking tenofovir (Viread, Gilead) and lamivudine (Epivir generic, Glaxo-SmithKline) were more likely to experience high BP than patients using zido-vudine (Retrovir, GlaxoSmithKline) and lamivudine medication. Tenofovir has been associated with a decline in renal function, the researchers note; their results suggest that the increase in risk, again, was mediated by BMI changes.
Although BP did not increase in all patients receiving indinavir drug, a subset of those patients who did develop hypertension had the highest rise among the cohort (more than a 40-mm Hg rise in systolic BP while using HAART). The researchers say this might represent secondary hypertension via a renal pathway. They advise further studies of, among other things, the role of intermediate variables such as lipoatrophy and lipohypertrophy in HIV-infected patients.