Key result
Eplerenone improves stress myocardial blood flow compared to placebo in people with HIV.
Why the study?
Increased RAAS activity may contribute to excess cardiovascular disease in people with HIV, but the effects of RAAS blockade on myocardial perfusion and function in this population are unclear.
Does eplerenone improve myocardial perfusion, injury, and function in people with HIV on stable ART without known heart disease?
RCT (n=40)
Double-blind
Randomized
Does eplerenone improve myocardial perfusion, injury, and function in people with HIV on stable ART without known heart disease?
In people with HIV on stable ART without known heart disease, RAAS blockade with eplerenone improved surrogate imaging markers of myocardial perfusion and function.
Eplerenone improves myocardial perfusion surrogates in HIV patients on stable ART without known heart disease; extends RAAS blockade evidence and supports outcome trials.
BACKGROUND: Increased renin angiotensin aldosterone system (RAAS) activity may contribute to excess cardiovascular disease in people with HIV (PWH). We investigated how RAAS blockade may improve myocardial perfusion, injury, and function among well-treated PWH. METHODS: Forty PWH, on stable ART, without known heart disease were randomized to eplerenone 50 mg PO BID (n = 20) or identical placebo (n = 20) for 12 months. The primary endpoints were (1) myocardial perfusion assessed by coronary flow reserve (CFR) on cardiac PET or stress myocardial blood flow (sMBF) on cardiac MRI or (2) myocardial inflammation by extracellular mass index (ECMi) on cardiac MRI. RESULTS: Beneficial effects on myocardial perfusion were seen for sMBF by cardiac MRI (mean [SD]: 0.09 [0.56] vs -0.53 [0.68] mL/min/g; P = .03) but not CFR by cardiac PET (0.01 [0.64] vs -0.07 [0.48]; P = .72, eplerenone vs placebo). Eplerenone improved parameters of myocardial function on cardiac MRI including left ventricular end diastolic volume (-13 [28] vs 10 [26] mL; P = .03) and global circumferential strain (GCS; median [interquartile range 25th-75th]: -1.3% [-2.9%-1.0%] vs 2.3% [-0.4%-4.1%]; P = .03), eplerenone versus placebo respectively. On cardiac MRI, improvement in sMBF related to improvement in global circumferential strain (ρ = -0.65, P = .057) among those treated with eplerenone. Selecting for those with impaired myocardial perfusion (CFR <2.5 and/or sMBF <1.8), there was a treatment effect of eplerenone versus placebo to improve CFR (0.28 [0.27] vs -0.05 [0.36]; P = .04). Eplerenone prevented a small increase in troponin (0.00 [-0.13-0.00] vs 0.00 [0.00-0.74] ng/L; P = .03) without effects on ECMi (0.9 [-2.3-4.3] vs -0.7 [-2.2--0.1] g/m2; P = .38). CD4+ T-cell count (127 [-38-286] vs -6 [-168-53] cells/μL; P = .02) increased in the eplerenone- versus placebo-treated groups. CONCLUSIONS: RAAS blockade with eplerenone benefitted key indices and prevented worsening of myocardial perfusion, injury, and function among PWH with subclinical cardiac disease when compared with placebo. CLINICAL TRIALS REGISTRATION: NCT02740179 (https://clinicaltrials.gov/ct2/show/NCT02740179?term=NCT02740179&draw=2&rank=1).
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Srinivasa et al. (2023) conducted an RCT in Human Immunodeficiency Virus (HIV) (n=40). Eplerenone vs. Identical placebo was evaluated on Myocardial perfusion assessed by coronary flow reserve (CFR) on cardiac PET or stress myocardial blood flow (sMBF) on cardiac MRI, or myocardial inflammation by extracellular mass index (ECMi) (p=0.03). Eplerenone improved stress myocardial blood flow (0.09 vs -0.53 mL/min/g; P=0.03) and myocardial function compared to placebo in people with HIV on stable ART.
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