Sodium–Glucose Cotransporter-2 Inhibitors After Acute Myocardial Infarction DOI Creative Commons

Nicia I. Profili,

Roberto Castelli, Roberto Manetti

и другие.

Biomedicines, Год журнала: 2025, Номер 13(3), С. 720 - 720

Опубликована: Март 15, 2025

Sodium–glucose cotransporter-2 inhibitors (SGLT2i) are a specific class of drugs originally developed for treating type 2 diabetes mellitus. Subsequently, studies demonstrated that their action was not limited to glycemic control but could also have positive effects on other outcomes, particularly at the cardiovascular level. Indeed, due diuretic effect, SGLT2i improve clinical chronic heart failure and reduce risk rehospitalization. In addition, reported protective effect major events mortality. More recently, it has been suggested prescription after an acute myocardial infarction may possible inflammation, arrhythmias, ventricular remodeling. Here, we reviewed focused in patients treated with percutaneous coronary intervention.

Язык: Английский

Cardiovascular outcomes with SGLT-2 inhibitors in individuals with diabetes and co-existing atrial fibrillation: A systematic review and meta-analysis DOI
Muhammad Zain Ameer, Muhammad Aemaz Ur Rehman,

Zunaira Amjad

и другие.

International Journal of Cardiology, Год журнала: 2025, Номер unknown, С. 133083 - 133083

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

1

Sodium-glucose cotransporter 2 inhibitors in transthyretin amyloid cardiomyopathy: navigating potential benefits and uncertainties DOI

Paschalis Karakasis

Current Medical Research and Opinion, Год журнала: 2025, Номер unknown, С. 1 - 9

Опубликована: Апрель 18, 2025

Sodium-glucose cotransporter-2 inhibitors (SGLT2i) have garnered attention for their potential role in managing transthyretin amyloid cardiomyopathy (ATTR-CM), a progressive condition characterized by significant morbidity and mortality. ATTR-CM remains underdiagnosed despite advances diagnostic modalities. While tafamidis acoramidis emerged as effective therapies, residual cardiovascular risk persists, highlighting the need adjunctive treatments. SGLT2i, initially developed antidiabetic agents, demonstrated cardioprotective effects various heart failure phenotypes, including preserved reduced ejection fractions. Emerging evidence suggests utility ATTR-CM, potentially addressing unmet needs such symptom burden, hospitalizations, survival. Clinical studies indicate that SGLT2i reduce all-cause mortality, major adverse cardiac events (MACE), with benefits extending to mortality improved functional status. Moreover, these agents appear mitigate arrhythmic complications, evidenced cardioversion procedures antiarrhythmic therapy requirements. Observational also highlight synergy of tafamidis, suggesting additive deposition failure. However, limitations, absence randomized controlled trials, immortal time bias, population heterogeneity, necessitate further research. Future directions involve elucidating mechanisms action, exploring personalized treatment strategies, leveraging big data analytics real-world insights. SGLT2i's transform management underscores promise, though robust trials are imperative validate findings optimize clinical applications.

Язык: Английский

Процитировано

1

Emerging opportunities to target inflammation: myocardial infarction and type 2 diabetes DOI Creative Commons
Tafadzwa T J Kufazvinei, Jason Chai,

Katherine A Boden

и другие.

Cardiovascular Research, Год журнала: 2024, Номер 120(11), С. 1241 - 1252

Опубликована: Июль 1, 2024

After myocardial infarction (MI), patients with type 2 diabetes have an increased rate of adverse outcomes, compared to without. Diabetes confers a 1.5-2-fold increase in early mortality and, importantly, this discrepancy has been consistent over recent decades, despite advances treatment and overall survival. Certain assumptions emerged explain risk, such as differences infarct size or coronary artery disease severity. Here, we re-evaluate that evidence show how contemporary analyses using state-of-the-art characterization tools suggest the received wisdom tells incomplete story. Simultaneously, epidemiological mechanistic biological data additional factors relating processes diabetes-related inflammation might play prominent role. Inflammatory after MI mediate injury repair are thus potential therapeutic target. Recent studies shown affects immune cell numbers drives changes bone marrow, leading pro-inflammatory gene expression functional suppression healing repair. review around prognosis MI, emphasis on targeting presents unexplored, yet valuable opportunities improve cardiovascular outcomes vulnerable patient group.

Язык: Английский

Процитировано

6

Safety and Efficacy of Early SGLT2 Inhibitors Initiation in Diabetic Patients Following Acute Myocardial Infarction, a Retrospective Study DOI Creative Commons

Gassan Moady,

Igor Yakubovich, Shaul Atar

и другие.

Journal of Cardiovascular Pharmacology and Therapeutics, Год журнала: 2024, Номер 29

Опубликована: Янв. 1, 2024

Introduction Sodium-glucose cotransporter- 2 (SGLT2) inhibitors have become a cornerstone in heart failure (HF), Type diabetes mellitus (T2DM), and cardiovascular disease (CVD) management. In the current retrospective study, we aimed to assess efficacy safety of SGLT2 early following acute myocardial infarction (AMI). Methods Patients with T2DM hospitalized for AMI 2017-2020 were divided according therapy status on discharge (with vs without therapy). Primary outcome was defined as composite hospitalizations HF, recurrent AMI, cerebrovascular accident (CVA). Secondary outcomes included any cause, total cumulative number hospitalizations, all-cause mortality. Results A 69 patients (mean age 59.2 ± 8.2 years) discharged compared 253 62.5 9.8) no inhibitors. During first year post-AMI, 4 (5.8%) treatment group 16 (6.3%) control CV events (p = 1.0). had lower rates hospitalization cause (31.9% 47.8%, P 0.02), change mortality (0% 3.6%, 0.21). After multivariate regression analysis, only female gender associated increased risk readmission, mainly due urinary tract infections. No diabetic ketoacidosis (DKA) or limb amputation reported. Conclusions We found that initiation is safe decreases cause.

Язык: Английский

Процитировано

5

Efficacy of Chronic Use of Sodium–Glucose Co-transporter 2 Inhibitors on the Prevention of Contrast-Induced Acute Kidney Injury in Patients with Type 2 Diabetes Mellitus Following Coronary Procedures: A Systematic Review and Meta-Analysis DOI
Kyriakos Dimitriadis, Angeliki Vakka, Nikolaos Pyrpyris

и другие.

American Journal of Cardiovascular Drugs, Год журнала: 2024, Номер unknown

Опубликована: Окт. 11, 2024

Язык: Английский

Процитировано

5

Atrial fibrillation: Epigenetic aspects and role of sodium-glucose cotransporter 2 inhibitors DOI Creative Commons

M. Donniacuo,

Antonella De Angelis,

Marialucia Telesca

и другие.

Pharmacological Research, Год журнала: 2022, Номер 188, С. 106591 - 106591

Опубликована: Дек. 9, 2022

Atrial fibrillation (AF) is the most frequent arrhythmia and associated with substantial morbidity mortality. Pathophysiological aspects consist in activation of pro-fibrotic signaling Ca2+ handling abnormalities at atrial level. Structural electrical remodeling creates a substrate for AF by triggering conduction cardiac arrhythmias. The care patients focuses predominantly on anticoagulation, symptoms control management risk factors comorbidities. goal therapy points to restore sinus rhythm, re-establish atrioventricular synchrony improve contribution stroke volume. New layer information better comprehend pathophysiology, identify targets novel pharmacological interventions consists epigenetic phenomena including, among others, DNA methylation, histone modifications noncoding RNAs. Moreover, benefits sodium-glucose cotransporter 2 inhibitors (SGLT2i) diabetic non-diabetic cardiovascular as well emerging evidence ability SGLT2i modify signature diseases provide solid background investigate possible role this drug class onset progression AF. In review, following summary pathophysiology management, mechanisms potential are discussed.

Язык: Английский

Процитировано

17

SGLT2 inhibitors: an evidence-based update on cardiovascular implications DOI

Imma Forzano,

Scott Wilson, Angela Lombardi

и другие.

Expert Opinion on Investigational Drugs, Год журнала: 2023, Номер 32(9), С. 839 - 847

Опубликована: Сен. 2, 2023

Introduction Sodium Glucose co-Transporter 2 (SGLT2) inhibitors (also known as 'gliflozins') represent a cornerstone to treat diabetes mellitus. Moreover, recent randomized clinical trials have demonstrated important cardioprotective effects of gliflozins, independent the presence diabetes. Herein, we summarize therapeutic progress in cardiovascular field obtained with SGLT2 inhibitors.

Язык: Английский

Процитировано

11

Obesity-induced Neuronal Senescence: Unraveling the Pathophysiological Links DOI
Puja Ghosh,

Rosaria Anna Fontanella,

Lucia Scisciola

и другие.

Ageing Research Reviews, Год журнала: 2024, Номер unknown, С. 102533 - 102533

Опубликована: Окт. 1, 2024

Язык: Английский

Процитировано

4

Effects and mechanisms of SGLT2 inhibitors on the NLRP3 inflammasome, with a focus on atherosclerosis DOI Creative Commons
Liu Yang, Xuejiao Zhang, Qing Wang

и другие.

Frontiers in Endocrinology, Год журнала: 2022, Номер 13

Опубликована: Дек. 15, 2022

Atherosclerosis is a lipid-driven chronic inflammatory disease that widespread in the walls of large and medium-sized arteries. Its pathogenesis not fully understood. The currently known includes activation pro-inflammatory signaling pathways body, increased oxidative stress, expression cytokines/chemokines. In innate immune response, vesicles are an important component with ability to promote maturation factors, release amounts cytokines, trigger cascade responses, clear pathogens damaged cells. Studies last few years have demonstrated NLRP3 play crucial role development atherosclerosis as well its complications. Several studies shown binding ligands promotes inflammasome formation, activates caspase-1, ultimately production IL-1β IL-18. IL-18 considered be two most prominent cytokines atherosclerosis. SGLT2 inhibitors novel hypoglycemic agents also significant antiatherosclerotic effects. However, their exact mechanism yet clear. This article review literature on effects mechanisms inflammasome, focusing antiatherosclerosis.

Язык: Английский

Процитировано

16

The Therapeutic Role of SGLT-2 Inhibitors in Acute Heart Failure: From Pathophysiologic Mechanisms to Clinical Evidence with Pooled Analysis of Relevant Studies across Safety and Efficacy Endpoints of Interest DOI Creative Commons
Dimitrios Patoulias, Nikolaos Fragakis, Manfredi Rizzo

и другие.

Life, Год журнала: 2022, Номер 12(12), С. 2062 - 2062

Опубликована: Дек. 8, 2022

(1) Background: Sodium-glucose co-transporter-2 (SGLT-2) inhibitors constitute a novel drug class with remarkable cardiovascular benefits for patients chronic heart failure (HF). Recently, this has been utilized in acute HF as an additional treatment option to classic diuretics, which remain the cornerstone of treatment. (2) Methods: We attempted identify those pathophysiologic mechanisms targeted by SGLT-2 inhibitors, could be benefit HF. then conducted comprehensive review literature within PubMed database order relevant studies, both randomized controlled trials (RCTs) and observational assessing safety efficacy (3) Results: induce significant osmotic diuresis natriuresis, decrease interstitial fluid volume blood pressure, improve left ventricular (LV) function, ameliorate LV remodeling prevent atrial arrhythmia occurrence, that seem beneficial However, currently available including six RCTs two real-world provide conflicting results concerning true “hard” surrogate endpoints. (4) Conclusions: Current evidence appears insufficient substantiate use Further are required shed more light on issue.

Язык: Английский

Процитировано

16