Normal myocardial flow reserve in HIV-infected patients on stable antiretroviral therapy: A cross-sectional study using rubidium-82 PET/CT

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Abstract

Studies have found HIV-infected patients to be at increased risk of myocardial infarction, which may be caused by coronary microvascular dysfunction. For the first time among HIV-infected patients, we assessed the myocardial flow reserve (MFR) by Rubidium-82 (82Rb) positron emission tomography (PET), which can quantify the coronary microvascular function. MFR has proved highly predictive of future coronary artery disease and cardiovascular events in the general population. In a prospective cross-sectional study, HIV-infected patients all receiving antiretroviral therapy (ART) with full viral suppression and HIV-uninfected controls were scanned using 82Rb PET/computed tomography at rest and adenosine-induced stress, thereby obtaining the MFR (stress flow/rest flow), stratified into low ≤1.5, borderline >1.5 to 2.0, or normal >2.0. Fifty-six HIV-infected patients and 25 controls were included. The HIV-infected patients had a mean age of 53 years (range 37-68 years) with 23% active smokers. The controls had a mean age of 52 years (range 36-68 years) and 26% active smokers. In the HIV-infected group 73% had a normal MFR, 17% borderline, and 10% low values of MFR. Among controls these values were 71%, 19%, and 10%, respectively (P=0.99). However, the HIV-infected group had lower values of stress myocardial blood flow (MBF) (2.63±0.09 mL/g/min vs 2.99± 0.14 mL/g/min; P=0.03). We found no evidence of decreased MFR as assessed by 82Rb PET among HIV-infected patients on stable ART with full viral suppression compared with HIV-uninfected controls. We did notice a decreased MBF during stress.

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Knudsen, A., Christensen, T. E., Ghotbi, A. A., Hasbak, P., Lebech, A. M., Kjær, A., & Ripa, R. S. (2015). Normal myocardial flow reserve in HIV-infected patients on stable antiretroviral therapy: A cross-sectional study using rubidium-82 PET/CT. Medicine (United States), 94(43). https://doi.org/10.1097/MD.0000000000001886

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