Heart rate-induced modifications of concentric left ventricular hypertrophy: exploration of a novel therapeutic concept

Author:

Klein Franziska J.1,Bell Stephen1,Runte K. Elisabeth1,Lobel Robert1,Ashikaga Takamuru2,Lerman Lilach O.3,LeWinter Martin M.1,Meyer Markus1

Affiliation:

1. Cardiology Division, University of Vermont College of Medicine, Burlington, Vermont;

2. Biostatistics Unit, University of Vermont College of Medicine, Burlington, Vermont; and

3. Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota

Abstract

Lowering the heart rate is considered to be beneficial in heart failure (HF) with reduced ejection fraction (HFrEF). In a dilated left ventricle (LV), pharmacological heart rate lowering is associated with a reduction in LV chamber size. In patients with HFrEF, this structural change is associated with better survival. HF with preserved ejection fraction (HFpEF) is increasingly prevalent but, so far, without any evidence-based treatment. HFpEF is typically associated with LV concentric remodeling and hypertrophy. The effects of heart rate on this structural phenotype are not known. Analogous with the benefits of a low heart rate on a dilated heart, we hypothesized that increased heart rates could lead to potentially beneficial remodeling of a concentrically hypertrophied LV. This was explored in an established porcine model of concentric LV hypertrophy and fibrosis. Our results suggest that a moderate increase in heart rate can be used to reduce wall thickness, normalize LV chamber volumes, decrease myocardial fibrosis, and improve LV compliance. Our results also indicate that the effects of heart rate can be titrated, are reversible, and do not induce HF. These findings may provide the rationale for a novel therapeutic approach for HFpEF and its antecedent disease substrate. Listen to this article’s corresponding podcast at http://ajpheart.podbean.com/e/heart-rate-modeling/ .

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI)

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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