Current Heart Failure Reports, Journal Year: 2024, Volume and Issue: 22(1)
Published: Nov. 15, 2024
Language: Английский
Current Heart Failure Reports, Journal Year: 2024, Volume and Issue: 22(1)
Published: Nov. 15, 2024
Language: Английский
The Lancet Diabetes & Endocrinology, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
3Journal of the American College of Cardiology, Journal Year: 2024, Volume and Issue: 84(17), P. 1678 - 1682
Published: Aug. 30, 2024
Language: Английский
Citations
9Journal of the American College of Cardiology, Journal Year: 2025, Volume and Issue: 85(2), P. 196 - 198
Published: Jan. 1, 2025
Language: Английский
Citations
1Drugs & Aging, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 18, 2025
Language: Английский
Citations
1JAMA Cardiology, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 17, 2024
Importance Sex is associated with the clinical presentation, outcomes, and response to treatment in patients heart failure (HF). However, little known about safety efficacy of finerenone according sex. Objective To estimate compared placebo both women men. Design, Setting, Participants Prespecified analyses were conducted phase 3 randomized trial Finerenone Trial Investigate Efficacy Safety Superior Placebo Patients Heart Failure (FINEARTS-HF). The was across 653 sites 37 countries. adults aged 40 years older symptomatic HF left ventricular ejection fraction (LVEF) 40% or greater between September 2020 January 2023. Intervention (titrated 20 mg mg) placebo. Main Outcomes Measures primary outcome a composite cardiovascular death total (first recurrent) events (unplanned hospitalizations urgent visits). Results A 6001 FINEARTS-HF, whom 2732 (45.5%), mean (SD) age 73.6 (9.1) years. Women had higher rates any obesity, LVEF (54.6 [7.6%] vs 50.9 [7.6] for men), lower estimated glomerular filtration rate than men (59.7 [19.1] 64.1 [20.0] men; P<.001) , worse New York Association functional class, Kansas City Cardiomyopathy Questionnaire-Total Symptom Scores (KCCQ-TSS) (mean [SD] 62.3 [24.0] 71.0 [23.1]). incident slightly (15.7; 95% CI, 14.3-17.3) (16.8; 15.4-18.3) per 100 person-years. Compared placebo, reduced risk end point similarly men: ratio 0.78 (95% 0.65-0.95) 0.88 0.74-1.04) ( P = .41 interaction). Consistent effects observed components all-cause mortality. increase (improvement) KCCQ-TSS from baseline 12 months finerenone, regardless sex .73 similar tolerability Conclusions Relevance In mildly preserved fraction. Registration ClinicalTrials.gov Identifier: NCT04435626
Language: Английский
Citations
4Trends in Endocrinology and Metabolism, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
0Journal of Cardiac Failure, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
0American Journal of Preventive Cardiology, Journal Year: 2025, Volume and Issue: unknown, P. 100928 - 100928
Published: Feb. 1, 2025
Language: Английский
Citations
0American Heart Journal Plus Cardiology Research and Practice, Journal Year: 2025, Volume and Issue: 52, P. 100518 - 100518
Published: March 1, 2025
Semaglutide, a GLP-1 receptor agonist, has emerged as promising agent in cardiovascular disease management, particularly for patients with obesity and diabetes. Recent studies have demonstrated significant benefits of Semaglutide beyond glycemic control, including reduced major adverse events (MACE), improvements heart failure symptoms, weight reduction. Notably, the STEP-HFpEF trial highlighted improved exercise capacity reduction NT-proBNP levels, offering novel therapeutic pathway management. Additionally, shown anti-inflammatory effects, reducing C-reactive protein (CRP) tumor necrosis factor-alpha (TNF-α), thereby mitigating atherosclerotic risks. Moreover, SELECT Semaglutide's non-diabetic, obese patients, suggesting that its effects extend loss. These findings represent potential paradigm shift risk although access affordability remain key challenges.
Language: Английский
Citations
0Pharmaceuticals, Journal Year: 2025, Volume and Issue: 18(3), P. 399 - 399
Published: March 12, 2025
This review addresses the role of semaglutide (SMG), a GLP-1 receptor agonist, in treatment obesity and its related comorbidities. Originally developed for type 2 diabetes (DM2), SMG has shown significant efficacy weight reduction, with superior results compared to other treatments same class. Its effects include appetite suppression, increased satiety, improvements cardiovascular, renal, metabolic parameters. Studies such as SUSTAIN, PIONEER, STEP highlight superiority agonists anti-obesity drugs. The oral formulation showed promising initial results, higher doses (50 mg) showing losses comparable those subcutaneous administration. Despite benefits, there are challenges, regain after cessation treatment, gastrointestinal adverse effects, variability response. Future studies should explore strategies mitigate these identify predictive factors efficacy, expand therapeutic indications conditions insulin resistance. constant innovation this class drugs reinforces potential transform protocols chronic weight-related diseases.
Language: Английский
Citations
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