Prevalence and prognostic significance of reduced myocardial perfusion reserve in diabetic heart failure with preserved ejection fraction using quantitative perfusion cardiac magnetic resonance DOI
Yang Yang,

Donglu Qin,

Chenyu Li

et al.

European Radiology, Journal Year: 2025, Volume and Issue: unknown

Published: March 5, 2025

Language: Английский

Heart Failure With Preserved Ejection Fraction DOI Creative Commons
Barry A. Borlaug, Kavita Sharma, Sanjiv J. Shah

et al.

Journal of the American College of Cardiology, Journal Year: 2023, Volume and Issue: 81(18), P. 1810 - 1834

Published: April 19, 2023

Language: Английский

Citations

241

Semaglutide in Patients with Obesity-Related Heart Failure and Type 2 Diabetes DOI
Mikhail Kosiborod, Mark C. Petrie, Barry A. Borlaug

et al.

New England Journal of Medicine, Journal Year: 2024, Volume and Issue: 390(15), P. 1394 - 1407

Published: March 28, 2024

Obesity and type 2 diabetes are prevalent in patients with heart failure preserved ejection fraction characterized by a high symptom burden. No approved therapies specifically target obesity-related persons diabetes.

Language: Английский

Citations

218

Obesity and heart failure with preserved ejection fraction: new insights and pathophysiological targets DOI
Barry A. Borlaug, Michael D. Jensen, Dalane W. Kitzman

et al.

Cardiovascular Research, Journal Year: 2022, Volume and Issue: 118(18), P. 3434 - 3450

Published: July 26, 2022

Abstract Obesity and heart failure with preserved ejection fraction (HFpEF) represent two intermingling epidemics driving perhaps the greatest unmet health problem in cardiovascular medicine 21st century. Many patients HFpEF are either overweight or obese, recent data have shown that increased body fat its attendant metabolic sequelae widespread, protean effects systemically on system leading to symptomatic HFpEF. The paucity of effective therapies underscores importance understanding distinct pathophysiological mechanisms obese develop novel therapies. In this review, we summarize current non-cardiovascular features phenotype HFpEF, how adiposity might pathophysiologically contribute phenotype, these processes be targeted therapeutically.

Language: Английский

Citations

200

Empagliflozin for Heart Failure With Preserved Left Ventricular Ejection Fraction With and Without Diabetes DOI Creative Commons
Gerasimos Filippatos, Javed Butler, Dimitrios Farmakis

et al.

Circulation, Journal Year: 2022, Volume and Issue: 146(9), P. 676 - 686

Published: Aug. 29, 2022

Background: Empagliflozin improves outcomes in patients with heart failure a preserved ejection fraction, but whether the effects are consistent and without diabetes remains to be elucidated. Methods: Patients class II through IV left ventricular fraction >40% were randomized receive empagliflozin 10 mg or placebo addition usual therapy. We undertook prespecified analysis comparing of versus diabetes. Results: Of 5988 enrolled, 2938 (49%) had The risk primary outcome (first hospitalization for cardiovascular death), total hospitalizations failure, estimated glomerular filtration rate decline was higher reduced irrespective status (hazard ratio, 0.79 [95% CI, 0.67, 0.94] hazard 0.78 0.64, 0.95] diabetes; P interaction =0.92). effect reduce also attenuate during double-blind treatment present diabetes, although more pronounced (1.77 0.98 mL/min/1.73m 2 =0.01). Across these 3 end points, did not differ prediabetes normoglycemia (33% 18% patient population, respectively). When investigated as continuous variable, baseline hemoglobin A1c modify on ( =0.26). There no increased hypoglycemic events either subgroup compared placebo. Conclusions: In enrolled EMPEROR-Preserved (Empagliflozin Outcome Trial With Chronic Heart Failure Preserved Ejection Fraction), significantly at baseline. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03057951.

Language: Английский

Citations

89

Association between the triglyceride glucose (TyG) index and the risk of acute kidney injury in critically ill patients with heart failure: analysis of the MIMIC-IV database DOI Creative Commons

Zewen Yang,

Hongxia Gong,

Fuqiang Kan

et al.

Cardiovascular Diabetology, Journal Year: 2023, Volume and Issue: 22(1)

Published: Aug. 31, 2023

Abstract Background Insulin resistance (IR) can be effectively assessed using the dependable surrogate biomarker triglyceride-glucose (TyG) index. In various critical care contexts, like contrast-induced acute kidney injury (AKI), an elevated TyG index has demonstrated a robust correlation with incidence of AKI. Nonetheless, potential to predict AKI in critically ill patients heart failure (HF) remains uncertain. Methods A cohort participants was non-consecutively selected from Medical Information Mart for Intensive Care IV (MIMIC-IV) database and divided into quartiles based on their values. The primary outcome. secondary endpoint in-hospital mortality within both whole study population subset patients. use renal replacement therapy (RRT) which represented progression severity also included as representing restricted cubic splines model Cox proportional hazards models were utilized evaluate association risk HF condition. Kaplan-Meier survival analysis employed estimate disparities across groups differentiated by Results This total 1,393 patients, 59% being male. 82.8%. analyses revealed significant between HF. illustrated linear relationship higher increased this specific patient population. Furthermore, unveiled statistically differences RRT Conclusions results highlight independent predictor poor outcome However, further confirmation causality necessitates larger prospective studies.

Language: Английский

Citations

56

2024 update in heart failure DOI Creative Commons

Alberto Beghini,

Antonio Maria Sammartino, Z. Papp

et al.

ESC Heart Failure, Journal Year: 2024, Volume and Issue: unknown

Published: May 28, 2024

Abstract In the last years, major progress has occurred in heart failure (HF) management. The 2023 ESC focused update of 2021 HF guidelines introduced new key recommendations based on results years science. First, two drugs, sodium–glucose co‐transporter‐2 (SGLT2) inhibitors and finerenone, a novel nonsteroidal, selective mineralocorticoid receptor antagonist (MRA), are recommended for prevention patients with diabetic chronic kidney disease (CKD). Second, SGLT2 now treatment across entire left ventricular ejection fraction spectrum. benefits quadruple therapy reduced (HFrEF) well established. Its rapid early up‐titration along close follow‐up frequent clinical laboratory re‐assessment after an episode acute (the so‐called ‘high‐intensity care’ strategy) was associated better outcomes STRONG‐HF trial. Patients experiencing worsening might require fifth drug, vericiguat. STEP‐HFpEF‐DM STEP‐HFpEF trials, semaglutide 2.4 mg once weekly administered 1 year decreased body weight significantly improved quality life 6 min walk distance obese preserved (HFpEF) or without history diabetes. Further data safety efficacy, including also hard endpoints, needed to support addition acetazolamide hydrochlorothiazide standard diuretic regimen hospitalized due HF. meantime, PUSH‐AHF supported use natriuresis‐guided therapy. options most recent evidence HF, specific drugs cardiomyopathies (i.e., mavacamten hypertrophic cardiomyopathy tafamidis transthyretin cardiac amyloidosis), device therapies, contractility modulation percutaneous valvulopathies, finding from TRILUMINATE Pivotal trial, reviewed this article.

Language: Английский

Citations

38

Finerenone and new-onset diabetes in heart failure: a prespecified analysis of the FINEARTS-HF trial DOI Creative Commons
Jawad H. Butt, Pardeep S. Jhund, Alasdair Henderson

et al.

The Lancet Diabetes & Endocrinology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Data on the effect of mineralocorticoid receptor antagonist therapy HbA1c levels and new-onset diabetes are conflicting. We aimed to examine oral finerenone, compared with placebo, incident in Finerenone Trial Investigate Efficacy Safety Superior Placebo Patients Heart Failure (FINEARTS-HF) trial. In this randomised, double-blind, placebo-controlled trial, 6001 participants heart failure New York Association functional class II-IV, left ventricular ejection fraction 40% or higher, evidence structural disease, elevated N-terminal pro-B-type natriuretic peptide were randomly assigned finerenone administered orally. Randomisation was performed concealed allocation. The primary outcome trial composite cardiovascular death total (first recurrent) events (ie, hospitalisation urgent visit). present analysis, at baseline (investigator-reported history ≥6·5%) excluded. New-onset defined as a measurement 6·5% higher two consecutive follow-up visits new initiation glucose-lowering therapy. full-analysis set comprised all study treatment, analysed according their treatment assignment irrespective received intention treat). safety analysis who took least one dose investigational product, actually received. This is registered ClinicalTrials.gov, NCT04435626, closed participants. Between Sept 14, 2020, Jan 10, 2023, recruited placebo. 3222 (53·7%) did not have population. During median duration 31·3 months (IQR 21·5-36·3), 115 (7·2%) group 147 (9·1%) placebo developed diabetes, corresponding rate 3·0 per 100 person-years (95% CI 2·5-3·6) 3·9 (3·3-4·6) group. Compared significantly reduced hazard by 24% (hazard ratio [HR] 0·76 [95% 0·59-0·97], p=0·026). Fine-Gray competing risk accounting for death, yielded similar finding (subdistribution HR 0·75 [0·59-0·96], p=0·024). Results sensitivity analyses, which definition expanded include SGLT2 inhibitor indication, restricted measurements only, drugs only (excluding treatment). Findings when treated excluded (n=15). consistent across key participant subgroups. Seven had an adverse event captured any definitions above. mildly preserved without representing meaningful additional clinical benefit these individuals. Bayer.

Language: Английский

Citations

2

Semaglutide in obesity-related heart failure with preserved ejection fraction and type 2 diabetes across baseline HbA1c levels (STEP-HFpEF DM): a prespecified analysis of heart failure and metabolic outcomes from a randomised, placebo-controlled trial DOI
Melanie J. Davies, Peter van der Meer, Subodh Verma

et al.

The Lancet Diabetes & Endocrinology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Language: Английский

Citations

2

How to Manage Heart Failure With Preserved Ejection Fraction DOI Creative Commons
Akshay S. Desai, Carolyn S.P. Lam, John J.V. McMurray

et al.

JACC Heart Failure, Journal Year: 2023, Volume and Issue: 11(6), P. 619 - 636

Published: May 3, 2023

Language: Английский

Citations

38

The Emerging Role of Glucagon-like Peptide-1 Receptor Agonists in the Management of Obesity-Related Heart Failure with Preserved Ejection Fraction: Benefits beyond What Scales Can Measure? DOI Creative Commons
Paschalis Karakasis, Nikolaos Fragakis, Dimitrios Patoulias

et al.

Biomedicines, Journal Year: 2024, Volume and Issue: 12(9), P. 2112 - 2112

Published: Sept. 16, 2024

Obesity is a significant predisposing factor for heart failure with preserved ejection fraction (HFpEF). Although substantial proportion of individuals HFpEF also have obesity, those obesity are under-represented in clinical trials failure. In turn, current guidelines provided limited recommendations the medical management this patient population. Both and diabetes induce pro-inflammatory state that can contribute to endothelial dysfunction coronary microvascular impairment, finally resulting HFpEF. Additionally, leads increased epicardial chest wall adiposity, which enhances ventricular interdependence. This condition further aggravated by plasma blood volume expansion excessive vasoconstriction, ultimately worsening Despite well-documented benefits GLP-1 receptor agonists subjects diabetes, or both, their role obesity-related remains unclear. light recently published literature, review aims investigate potential mechanisms synthesize available evidence regarding patients

Language: Английский

Citations

14