Related Experiment Video
Updated: May 8, 2026

Comprehensive Echocardiographic Assessment of Right Ventricle Function in a Rat Model of Pulmonary Arterial Hypertension
Published on: January 20, 2023
Eplerenone in systemic right ventricle: double blind randomized clinical trial. The evedes study
Laura Dos1, Sandra Pujadas, Montserrat Estruch
1Integrated Adult Congenital Heart Disease Unit of Vall d'Hebron University Hospital and Santa Creu i Sant Pau University Hospital, Barcelona, Spain; Autonomous University of Barcelona, Spain.
Eplerenone treatment in patients with a failing systemic right ventricle (SRV) showed a trend toward reducing collagen turnover biomarkers, suggesting potential for treating myocardial fibrosis.
Area of Science:
- Cardiology
- Pharmacology
- Biomarkers
Background:
- No established pharmacological treatments exist for failing systemic right ventricle (SRV).
- Myocardial fibrosis is implicated in the pathophysiology of SRV.
Purpose of the Study:
- To evaluate the effects of eplerenone on cardiac parameters and collagen turnover biomarkers in patients with SRV.
- To assess eplerenone's potential in managing myocardial fibrosis in SRV.
Main Methods:
- A 12-month, double-blind, placebo-controlled clinical trial.
- Assessed SRV mass, ejection fraction, neurohormonal levels, and collagen turnover biomarkers (CTBs) using cardiac MRI.
- Included 26 patients with SRV post-atrial switch repair and 14 healthy controls.
Main Results:
- Patients with SRV exhibited elevated levels of NT-proBNP, CICP, and ICTP compared to controls.
- Eplerenone treatment showed a trend towards reducing CICP, NT-proMMP1, TIMP1, and galectin 3, with a lower increase in ICTP.
- Eplerenone did not conclusively reduce SRV mass or improve SRV function.
Conclusions:
- Eplerenone improved the altered collagen turnover biomarker profile in SRV patients.
- Reduction of myocardial fibrosis may represent a viable therapeutic target for SRV.
Related Concept Videos
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme (ECE). Of...
Antihypertensive Drugs: Direct Renin Inhibitors
Heart Failure Drugs: Diuretics
Heart Failure Drugs: β-Blockers
Antihypertensive Drugs: Angiotensin II Receptor Blockers
