Literature DB >> 31584231

Evaluation of the effect of sodium-glucose co-transporter 2 inhibition with empagliflozin on morbidity and mortality of patients with chronic heart failure and a reduced ejection fraction: rationale for and design of the EMPEROR-Reduced trial.

Milton Packer1,2, Javed Butler3, Gerasimos S Filippatos4,5, Waheed Jamal6, Afshin Salsali7, Janet Schnee7, Karen Kimura8, Cordula Zeller9, Jyothis George6, Martina Brueckmann6,10, Stefan D Anker11, Faiez Zannad12.   

Abstract

Drugs that inhibit the sodium-glucose co-transporter 2 (SGLT2) have been shown to reduce the risk of hospitalizations for heart failure in patients with type 2 diabetes. In populations that largely did not have heart failure at the time of enrolment, empagliflozin, canagliflozin and dapagliflozin decreased the risk of serious new-onset heart failure events by ≈30%. In addition, in the EMPA-REG OUTCOME trial, empagliflozin reduced the risk of both pump failure and sudden deaths, the two most common modes of death among patients with heart failure. In none of the three trials could the benefits of SGLT2 inhibitors on heart failure be explained by the actions of these drugs as diuretics or anti-hyperglycaemic agents. These observations raise the possibility that SGLT2 inhibitors could reduce morbidity and mortality in patients with established heart failure, including those without diabetes. The EMPEROR-Reduced trial is enrolling ≈3600 patients with heart failure and a reduced left ventricular ejection fraction (≤ 40%), half of whom are expected not to have diabetes. Patients are being randomized to placebo or empagliflozin 10 mg daily, which is added to all appropriate treatment with inhibitors of the renin-angiotensin system and neprilysin, beta-blockers and mineralocorticoid receptor antagonists. The primary endpoint is the time-to-first event analysis of the combined risk of cardiovascular death and hospitalization for heart failure, but the trial will also evaluate the effects of empagliflozin on renal function, cardiovascular death, all-cause mortality, and recurrent hospitalization events. By adjusting eligibility based on natriuretic peptide levels to the baseline ejection fraction, the trial will preferentially enrol high-risk patients. A large proportion of the participants is expected to have an ejection fraction < 30%, and the estimated annual event rate is expected to be at least 15%. The EMPEROR-Reduced trial is well-positioned to determine if the addition of empagliflozin can add meaningfully to current approaches that have established benefits in the treatment of chronic heart failure with left ventricular systolic dysfunction.
© 2019 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Entities:  

Keywords:  Diabetes; Heart failure; Reduced ejection fraction; SGLT2 inhibitors; Trial design

Year:  2019        PMID: 31584231     DOI: 10.1002/ejhf.1536

Source DB:  PubMed          Journal:  Eur J Heart Fail        ISSN: 1388-9842            Impact factor:   15.534


  39 in total

1.  The year in cardiology: heart failure.

Authors:  John G F Cleland; Alexander R Lyon; Theresa McDonagh; John J V McMurray
Journal:  Eur Heart J       Date:  2020-03-21       Impact factor: 29.983

Review 2.  Empagliflozin for Patients with Heart Failure and Type 2 Diabetes Mellitus: Clinical Evidence in Comparison with Other Sodium-Glucose Co-transporter-2 Inhibitors and Potential Mechanism.

Authors:  Bo Liang; Rui Li; Peng Zhang; Ning Gu
Journal:  J Cardiovasc Transl Res       Date:  2022-08-15       Impact factor: 3.216

Review 3.  Glucose-Lowering Therapy beyond Insulin in Type 1 Diabetes: A Narrative Review on Existing Evidence from Randomized Controlled Trials and Clinical Perspective.

Authors:  Felix Aberer; Thomas R Pieber; Max L Eckstein; Harald Sourij; Othmar Moser
Journal:  Pharmaceutics       Date:  2022-05-31       Impact factor: 6.525

Review 4.  Hypertension and Type 2 Diabetes-The Novel Treatment Possibilities.

Authors:  Agnieszka Przezak; Weronika Bielka; Andrzej Pawlik
Journal:  Int J Mol Sci       Date:  2022-06-10       Impact factor: 6.208

Review 5.  Challenges of Cardio-Kidney Composite Outcomes in Large-Scale Clinical Trials.

Authors:  Ravi B Patel; Jozine M Ter Maaten; João Pedro Ferreira; Finnian R McCausland; Sanjiv J Shah; Patrick Rossignol; Scott D Solomon; Muthiah Vaduganathan; Milton Packer; Aliza Thompson; Norman Stockbridge; Faiez Zannad
Journal:  Circulation       Date:  2021-01-07       Impact factor: 29.690

6.  Dipeptidyl peptidase-4 inhibitors, glucagon-like peptide 1 receptor agonists and sodium-glucose co-transporter-2 inhibitors for people with cardiovascular disease: a network meta-analysis.

Authors:  Takayoshi Kanie; Atsushi Mizuno; Yoshimitsu Takaoka; Takahiro Suzuki; Daisuke Yoneoka; Yuri Nishikawa; Wilson Wai San Tam; Jakub Morze; Andrzej Rynkiewicz; Yiqiao Xin; Olivia Wu; Rui Providencia; Joey Sw Kwong
Journal:  Cochrane Database Syst Rev       Date:  2021-10-25

Review 7.  Sodium glucose cotransporter (SGLT)-2 inhibitors alleviate the renal stress responsible for sympathetic activation.

Authors:  Motoaki Sano
Journal:  Ther Adv Cardiovasc Dis       Date:  2020 Jan-Dec

Review 8.  The Diabetic Cardiomyopathy: The Contributing Pathophysiological Mechanisms.

Authors:  Teresa Salvatore; Pia Clara Pafundi; Raffaele Galiero; Gaetana Albanese; Anna Di Martino; Alfredo Caturano; Erica Vetrano; Luca Rinaldi; Ferdinando Carlo Sasso
Journal:  Front Med (Lausanne)       Date:  2021-06-30

9.  The impact of empagliflozin on cardiac physiology and fibrosis early after myocardial infarction in non-diabetic rats.

Authors:  Elias Daud; Offir Ertracht; Nadav Bandel; Gassan Moady; Monah Shehadeh; Tali Reuveni; Shaul Atar
Journal:  Cardiovasc Diabetol       Date:  2021-07-02       Impact factor: 9.951

10.  Different effects of SGLT2 inhibitors according to the presence and types of heart failure in type 2 diabetic patients.

Authors:  In-Chang Hwang; Goo-Yeong Cho; Yeonyee E Yoon; Jin Joo Park; Jun-Bean Park; Seung-Pyo Lee; Hyung-Kwan Kim; Yong-Jin Kim; Dae-Won Sohn
Journal:  Cardiovasc Diabetol       Date:  2020-05-28       Impact factor: 9.951

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