Literature DB >> 27545139

Novel Therapies for Heart Failure - Where Do They Stand?

Barry Greenberg1.   

Abstract

Despite advances in therapy, patients with heart failure (HF) continue to experience unacceptably high rates of hospitalization and death, as well as poor quality of life. As a consequence, there is an urgent need for new treatments that can improve the clinical course of the growing worldwide population of HF patients. Serelaxin and ularatide, both based on naturally occurring peptides, have potent vasodilatory as well as other effects on the heart and kidneys. For both agents, phase 3 studies that are designed to determine whether they improve outcomes in patients with acute HF have completed enrollment. TRV027, a biased ligand for the type 1 angiotensin receptor with effects that extend beyond traditional angiotensin-receptor blockers is also being studied in the acute HF population. Omecamtiv mecarbil, an inotropic agent that improves myocardial contractility by a novel mechanism, and vericiguat, a drug that stimulates soluble guanylate cyclase, are both being developed to treat patients with chronic HF. Finally, despite the negative results of the CUPID study, gene transfer therapy continues to be explored as a means of improving the function of the failing heart. The basis for the use of these drugs and their current status in clinical trials are discussed. (Circ J 2016; 80: 1882-1891).

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Year:  2016        PMID: 27545139     DOI: 10.1253/circj.CJ-16-0742

Source DB:  PubMed          Journal:  Circ J        ISSN: 1346-9843            Impact factor:   2.993


  7 in total

Review 1.  The Diverse Roles of Arrestin Scaffolds in G Protein-Coupled Receptor Signaling.

Authors:  Yuri K Peterson; Louis M Luttrell
Journal:  Pharmacol Rev       Date:  2017-07       Impact factor: 25.468

2.  Novel high molecular weight albumin-conjugated angiotensin II activates β-arrestin and G-protein pathways.

Authors:  Hong Weng Pang; Andrea Linares; Leena Couling; Jessica Santollo; Leonardo Ancheta; Derek Daniels; Robert C Speth
Journal:  Endocrine       Date:  2019-04-24       Impact factor: 3.633

3.  Dose-Dependent Effects of the Myosin Activator Omecamtiv Mecarbil on Cross-Bridge Behavior and Force Generation in Failing Human Myocardium.

Authors:  Ranganath Mamidi; Jiayang Li; Kenneth S Gresham; Sujeet Verma; Chang Yoon Doh; Amy Li; Sean Lal; Cristobal G Dos Remedios; Julian E Stelzer
Journal:  Circ Heart Fail       Date:  2017-10       Impact factor: 8.790

4.  Angiotensin II activates CaV 1.2 Ca2+ channels through β-arrestin2 and casein kinase 2 in mouse immature cardiomyocytes.

Authors:  Toshihide Kashihara; Tsutomu Nakada; Katsuhiko Kojima; Toshikazu Takeshita; Mitsuhiko Yamada
Journal:  J Physiol       Date:  2017-04-20       Impact factor: 5.182

Review 5.  Structural Insights into Ligand-Receptor Interactions Involved in Biased Agonism of G-Protein Coupled Receptors.

Authors:  Krzysztof Jóźwiak; Anita Płazińska
Journal:  Molecules       Date:  2021-02-06       Impact factor: 4.411

Review 6.  Targeting Obesity and Diabetes to Treat Heart Failure with Preserved Ejection Fraction.

Authors:  Raffaele Altara; Mauro Giordano; Einar S Nordén; Alessandro Cataliotti; Mazen Kurdi; Saeed N Bajestani; George W Booz
Journal:  Front Endocrinol (Lausanne)       Date:  2017-07-17       Impact factor: 5.555

Review 7.  The metabolic model of heart failure: the role of sodium glucose co-transporter-2 (SGLT-2) inhibition.

Authors:  Muhammad Saad; Umut Gomceli; Pranav Ravi; Andrisael G Lacoste; Neil Shah; Timothy J Vittorio
Journal:  Drugs Context       Date:  2018-11-21
  7 in total

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