Prevention & lipidsRandomised controlled trial

Mineralocorticoid Receptor Antagonism by Eplerenone and Arterial Inflammation in HIV

JAMA CardiolPublished

  • Randomised controlled trial
  • double-blind
  • placebo-controlled
  • substudy of MIRACLE HIV

Authors' conclusion

In this small randomized clinical trial, eplerenone was associated with reduction in arterial inflammation among well-treated PWH without known CVD. In addition, reductions in arterial inflammation as measured by 18F-FDG PET/CT were related to improvements in stress myocardial perfusion.

Study context

Population
Well-treated persons with HIV without known cardiovascular disease (CVD) and no current statin use
Participants
26 persons
Comparison
Eplerenone vs placebo
  • Eplerenonen = 13
  • Placebon = 13reference
Primary endpoint
Change in target to background ratio (TBR, arterial wall inflammation) in the index vessel (highest baseline TBR: aorta, left or right carotid) on 18F-FDG PET/CT
Follow-up
12 months

Primary result

TBR of index vessel

Model treatment effect

−0.31

95% CI −0.50 to −0.11

P = 0.006

By group

Eplerenone

−12.4%

percentage change · IQR −21.9%–-2.6%

Placebo

5.1%

percentage change · IQR −1.6%–11.0%

As reported in the abstract

Further findings

Percentage change

OutcomeEplerenonePlaceboP value
TBR of most diseased segment (MDS) of index vessel−19.1% (IQR −27.0%–-11.9%)6.8% (IQR −9.1%–12.1%)P = 0.007
TBR of carotid index vessel−10.0% (IQR −21.8%–3.6%)9.7% (IQR −9.8%–15.9%)P = 0.046

Correlation of most diseased segment (MDS) to background ratio (TBR) reduction with improvement in stress myocardial blood flow on CMR

Spearman ρ
−0.67; P = .01

Original publication

Mineralocorticoid Receptor Antagonism by Eplerenone and Arterial Inflammation in HIV. JAMA Cardiol. Published 1 February 2024. doi:10.1001/jamacardio.2023.4578

Summarised from the published abstract; every number is checked against it