Heart failure with reduced ejection fraction and the intersection of cardio-renal-metabolic medicine #CaReMe

Author:

Marx Nikolaus1ORCID,Cheng Alice Y Y2,Agarwal Rajiv3,Greene Stephen J45,Abuhantash Hadi6

Affiliation:

1. Department of Internal Medicine I, University Hospital Aachen, RWTH Aachen University , Pauwelsstraße 30, D-52074 Aachen , Germany

2. Trillium Health Partners and Unity Health Toronto, Department of Medicine, University of Toronto , 507-2300 Eglinton Avenue West, Mississauga, Ontario L5M 2V8 , Canada

3. Department of Medicine, Division of Nephrology, Indiana University School of Medicine and Richard L. Roudebush VA Medical Center , 1481 West 10th St, 111N Indianapolis, IN 46202 , USA

4. Division of Cardiology Advanced Heart Failure & Transplantation, Duke Clinical Research Institute , 40 Duke Medicine CircleClinic 2K Room 2250, Orange Zone Durham, NC 27710 , USA

5. Division of Cardiology, Duke University School of Medicine , 40 Duke Medicine CircleClinic 2K Room 2250, Orange Zone Durham, NC 27710 , USA

6. Department of Cardiology, University of Jordan , Amman PO Box 815447 , Jordan

Abstract

Abstract Diabetes and chronic kidney disease (CKD) are important comorbidities in patients with heart failure (HF) that can complicate the clinical management and have major implications for morbidity and mortality. In addition, the presence of these comorbidities, particularly advanced CKD, is a limitation for the implementation of guideline-directed therapies in patients with HF with reduced ejection fraction (HFrEF). Though clinical trials in patients with HFrEF trials included varying percentages of patients with diabetes and/or CKD, patients with advanced CKD have been excluded in most HF studies. Thus, management recommendations for these patients often have to be extrapolated from subgroup analyses. This article summarizes pathophysiological aspects of the interaction of HFrEF, CKD, and diabetes and addresses clinical aspects for the screening of these comorbidities. Moreover, current treatment options for patients with HFrEF and CKD and/or diabetes are discussed and novel strategies such as the use of the selective mineralocorticoid receptor antagonist Finerenone are addressed.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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