Acyl ghrelin increases cardiac output while preserving right ventricular‐pulmonary arterial coupling in heart failure

Author:

Erhardsson Mikael1,Faxén Ulrika L.12,Venkateshvaran Ashwin34,Hage Camilla15,Pironti Gianluigi16,Thorvaldsen Tonje15,Webb Dominic‐Luc7,Hellström Per M.7,Andersson Daniel C.156,Ståhlberg Marcus15,Lund Lars H.15

Affiliation:

1. Department of Medicine, Unit of Cardiology Karolinska Institutet Stockholm Sweden

2. Department of Perioperative Medicine and Intensive Care Karolinska University Hospital Stockholm Sweden

3. Department of Clinical Physiology, Department of Clinical Sciences Lund University Stockholm Sweden

4. Skåne University Hospital Lund Sweden

5. Department of Heart and Vascular Theme Karolinska University Hospital Stockholm Sweden

6. Department of Physiology and Pharmacology Karolinska Institutet Stockholm Sweden

7. Department of Medical Sciences, Gastroenterology and Hepatology Uppsala University Uppsala Sweden

Abstract

AbstractAimAcyl ghrelin increases cardiac output (CO) in heart failure with reduced ejection fraction (HFrEF). This could impair the right ventricular‐pulmonary arterial coupling (RVPAC), both through an increased venous return and right ventricular afterload. We aim to investigate if acyl ghrelin increases CO with or without worsening the right‐sided haemodynamics in HFrEF assessed by RVPAC.Methods and resultsThe Karolinska Acyl ghrelin Trial was a randomized double‐blind placebo‐controlled trial of acyl ghrelin versus placebo (120‐min intravenous infusion) in HFrEF. RVPAC was assessed echocardiographically at baseline and 120 min. ANOVA was used for difference in change between acyl ghrelin versus placebo, adjusted for baseline values. Of the 30 randomized patients, 22 had available RVPAC (acyl ghrelin n = 12, placebo n = 10). Despite a 15% increase in CO in the acyl ghrelin group (from 4.0 (3.5–4.6) to 4.6 (3.9–6.1) L/min, P = 0.003), RVPAC remained unchanged; 5.9 (5.3–7.6) to 6.3 (4.8–7.5) mm·(m/s)−1, P = 0.372, while RVPAC was reduced in the placebo group, 5.2 (4.3–6.4) to 4.8 (4.2–5.8) mm·(m/s)−1, P = 0.035. Comparing change between groups, CO increased in the acyl ghrelin group versus placebo (P = 0.036) while RVPAC and the right ventricular pressure gradient remained unchanged.ConclusionTreatment with acyl ghrelin increases CO while preserving or even improving RVPAC in HFrEF, possibly due to increased contractility, reduced PVR and/or reduced left sided filling pressures. These potential effects strengthen the role of acyl ghrelin therapy in HFrEF with right ventricular failure.

Funder

Hjärt-Lungfonden

Karolinska Institutet

Stockholms Läns Landsting

Vetenskapsrådet

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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