SGLT-2 inhibitors on cardiac autonomic function in individuals with and without type 2 diabetes mellitus DOI
Hasan Fehmi Özel, Şüheda Alpay,

Emre Asker

и другие.

Journal of Diabetes and its Complications, Год журнала: 2025, Номер unknown, С. 109021 - 109021

Опубликована: Март 1, 2025

Язык: Английский

Outcomes in diabetic patients treated with SGLT2-Inhibitors with acute myocardial infarction undergoing PCI: The SGLT2-I AMI PROTECT Registry DOI Creative Commons
Pasquale Paolisso, Luca Bergamaschi, Felice Gragnano

и другие.

Pharmacological Research, Год журнала: 2022, Номер 187, С. 106597 - 106597

Опубликована: Дек. 5, 2022

To investigate in-hospital and long-term prognosis in T2DM patients presenting with acute myocardial infarction (AMI) treated SGLT2-I versus other oral anti-diabetic agents (non-SGLT2-I users).

Язык: Английский

Процитировано

92

Canagliflozin mitigates ferroptosis and improves myocardial oxidative stress in mice with diabetic cardiomyopathy DOI Creative Commons
Shuqin Du, Hanqiang Shi, Lie Xiong

и другие.

Frontiers in Endocrinology, Год журнала: 2022, Номер 13

Опубликована: Окт. 14, 2022

Canagliflozin (Cana), an anti-diabetes drug belongs to sodium-glucose cotransporter 2 inhibitor, is gaining interest because of its extra cardiovascular benefits. Ferroptosis a new mode cell death, which can promote the occurrence diabetic cardiomyopathy (DCM). Whether Cana alleviate DCM by inhibiting ferroptosis focus this study. Here, we induced models in C57BL6 mice and treated with Cana. Meanwhile, order exclude hypoglycemic effect, high glucose model H9C2 cells were established. In vivo study, observed that could effectively damage cardiac function mice, including increasing lactate dehydrogenase (LDH) troponin I (cTnI), alleviating myocardial fiber breakage, inflammation, collagen deposition mitochondrial structural disorder. We evaluated reactive oxygen species (ROS) levels DCFH-DA BODIPY 581/591 C11, vitro reduced ROS lipid glucose. JC-1 fluorochrome assay showed decreased membrane potential (MMP) was increased Furthermore, inhibitory effects on oxidative stress verified protein carbonyl (PCO), malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione (GSH). As key inducer ferroptosis, total iron Fe 2+ be inhibited both . addition, western blot results indicated expression ferritin heavy-chain (FTN-H) down-regulated, cystine-glutamate antiporter (xCT) up-regulated cells, suggesting inhibit balancing homeostasis promoting system Xc - /GSH/GPX4 axis DCM. These findings underscore fact plays important role development progression targeting may novel strategy for prevention treatment. conclusion, exert some benefits attenuating ferroptosis.

Язык: Английский

Процитировано

84

Impact of SGLT2-inhibitors on contrast-induced acute kidney injury in diabetic patients with acute myocardial infarction with and without chronic kidney disease: Insight from SGLT2-I AMI PROTECT registry DOI
Pasquale Paolisso, Luca Bergamaschi, Arturo Cesaro

и другие.

Diabetes Research and Clinical Practice, Год журнала: 2023, Номер 202, С. 110766 - 110766

Опубликована: Июнь 3, 2023

Язык: Английский

Процитировано

48

SGLT2-inhibitors in diabetic patients with severe aortic stenosis and cardiac damage undergoing transcatheter aortic valve implantation (TAVI) DOI Creative Commons

Pasquale Paolisso,

Marta Belmonte, Emanuele Gallinoro

и другие.

Cardiovascular Diabetology, Год журнала: 2024, Номер 23(1)

Опубликована: Ноя. 21, 2024

A substantial number of patients with severe aortic stenosis (AS) undergoing transcatheter valve implantation (TAVI) experience adverse events after TAVI, health care expenditure. We aimed to investigate cardiac remodeling and long-term outcomes in diabetic AS, left ventricular ejection fraction (LVEF) < 50%, extra-valvular damage (EVCD) TAVI treated sodium-glucose cotransporter-2 inhibitors (SGLT2i) versus other glucose-lowering strategies (no-SGLT2i users). Multicenter international registry consecutive LVEF EVCD TAVI. Based on therapy at hospital discharge, were stratified SGLT2i no-SGLT2i users. The primary endpoint was a composite all-cause death heart failure (HF)-hospitalization (major cardiovascular events, MACE) 2-year follow-up. Secondary included death, HF hospitalization. study population 311 patients, among which 24% Within 1-year users experienced higher rate LV recovery (p = 0.032), especially those baseline ≤ 30% 0.026), despite the lower LVEF. Patients not more likely progress worse stage over time 0.018). At follow-up, use associated MACE, hospitalization 0.01 for all). After adjusting confounding factors, emerged as an independent predictor reduced MACE (HR 0.45; 95% CI 0.17–0.75; p 0.007), 0.51; 0.25–0.98; 0.042) HF-hospitalization 0.40; 0.27–0.62; 0.004). In favorable risk

Язык: Английский

Процитировано

23

Comparative Effectiveness of Individual Sodium-Glucose Cotransporter 2 Inhibitors DOI
HoJin Shin, Julie M. Paik, Brendan M. Everett

и другие.

JAMA Internal Medicine, Год журнала: 2025, Номер unknown

Опубликована: Янв. 21, 2025

Importance Evidence on cardiovascular benefits and safety of sodium-glucose cotransporter 2 (SGLT-2) inhibitors is mainly from placebo-controlled trials. Therefore, the comparative effectiveness individual SGLT-2 remain unknown. Objective To compare use canagliflozin or dapagliflozin with empagliflozin for a composite outcome (myocardial infarction [MI] stroke), heart failure hospitalization, MI, stroke, all-cause death, outcomes, including diabetic ketoacidosis (DKA), lower-limb amputation, bone fracture, severe urinary tract infection (UTI), genital whether effects differed by dosage disease (CVD) history. Design, Setting, Participants This study using target trial emulation included adults type diabetes (T2D) 3 US claims databases data August 2014 through June 2020. The was conducted 2023 to July 2024, follow-up period up 8 years, analysis completed in 2024. Exposures First dispensing canagliflozin, dapagliflozin, without any during prior 365 days. Main outcomes measures Database-specific models were weighted propensity score matching-weights adjust 129 confounders. Hazard ratios 95% CIs estimated Cox proportional hazards models. HRs pooled across fixed-effect meta-analysis. Results : Across databases, 232 890 patients receiving 881 295 043 identified. Compared initiators, those less likely have diabetes-related conditions history CVD at baseline. For MI/stroke risk, both (HR, 0.98; CI, 0.91-1.05) 0.95; 0.89-1.03) comparable empagliflozin. initiators had higher risk 1.19; 1.02-1.39), particularly low dose 5 mg 1.30; 1.12-1.50). These findings consistent subgroups events, compared empagliflozin, lower infections 0.94; 0.91-0.97) but UTIs 1.13; 1.03-1.24), risks 0.92; 0.89-0.95) DKA 0.78; 0.68-0.90). Conclusions Relevance found that demonstrated clinically effective doses, though low-dose showed reduced benefit hospitalization

Язык: Английский

Процитировано

3

In-hospital arrhythmic burden reduction in diabetic patients with acute myocardial infarction treated with SGLT2-inhibitors: Insights from the SGLT2-I AMI PROTECT study DOI Creative Commons
Arturo Cesaro, Felice Gragnano, Pasquale Paolisso

и другие.

Frontiers in Cardiovascular Medicine, Год журнала: 2022, Номер 9

Опубликована: Сен. 27, 2022

Sodium-glucose co-transporter 2 inhibitors (SGLT2-i) have shown significant cardiovascular benefits in patients with and without type diabetes mellitus (T2DM). They also gained interest for their potential anti-arrhythmic role ability to reduce the occurrence of atrial fibrillation (AF) ventricular arrhythmias (VAs) T2DM heart failure patients.To investigate in-hospital new-onset cardiac a cohort presenting acute myocardial infarction (AMI) treated SGLT2-i vs. other oral anti-diabetic agents (non-SGLT2-i users).Patients from SGLT2-I AMI PROTECT registry (NCT05261867) were stratified according use before admission AMI, divided into users non-SGLT2-i users. In-hospital outcomes included (NOCAs), defined as composite AF sustained tachycardia (VT) and/or (VF) during hospitalization.The study population comprised 646 categorized (111 patients) (535 patients). had lower rate NOCAs compared (6.3 15.7%, p = 0.010). Moreover, was associated VT/VF considered individually (p 0.032). In multivariate logistic regression model, after adjusting all confounding factors, identified an independent predictor (OR 0.35; 95%CI 0.14-0.86; 0.022). At multinomial regression, confounders, therapy remained 0.20; 0.04-0.97; 0.046) but not occurrence.In patients, risk arrhythmic events hospitalization AMI. particular, primary effect expressed reduction VAs. These findings emphasize cardioprotective effects setting beyond glycemic control.Data are part observational international registry: PROTECT. ClinicalTrials.gov, identifier: NCT05261867.

Язык: Английский

Процитировано

63

Obesity, diabetes mellitus, and cardiometabolic risk: An Obesity Medicine Association (OMA) Clinical Practice Statement (CPS) 2023 DOI Creative Commons
Harold Bays,

Shagun Bindlish,

Tiffany Lowe Clayton

и другие.

Obesity Pillars, Год журнала: 2023, Номер 5, С. 100056 - 100056

Опубликована: Янв. 28, 2023

This Obesity Medicine Association (OMA) Clinical Practice Statement (CPS) is intended to provide clinicians an overview of type 2 diabetes mellitus (T2DM), obesity-related cardiometabolic risk factor.

Язык: Английский

Процитировано

32

Hypertrophic cardiomyopathy dysfunction mimicked in human engineered heart tissue and improved by sodium–glucose cotransporter 2 inhibitors DOI Creative Commons

Paul J.M. Wijnker,

Rafeeh Dinani,

Nico C van der Laan

и другие.

Cardiovascular Research, Год журнала: 2024, Номер 120(3), С. 301 - 317

Опубликована: Янв. 18, 2024

Abstract Aims Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy, often caused by pathogenic sarcomere mutations. Early characteristics of HCM are diastolic dysfunction and hypercontractility. Treatment to prevent mutation-induced cardiac lacking. Sodium–glucose cotransporter 2 inhibitors (SGLT2i) a group antidiabetic drugs that recently showed beneficial cardiovascular outcomes in patients with acquired forms heart failure. We here studied if SGLT2i represent potential therapy correct cardiomyocyte induced an mutation. Methods results Contractility was measured human pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) harbouring mutation cultured 2D 3D engineered tissue (EHT). Mutations gene encoding β-myosin heavy chain (MYH7-R403Q) or troponin T (TNNT2-R92Q) were investigated. In 2D, intracellular [Ca2+], action ion currents determined. mutations hiPSC-CMs impaired relaxation increased force, mimicking early features observed HCM. enhance hiPSC-CMs, larger extent compared control hiPSC-CMs. Moreover, SGLT2i-effects on R403Q EHT culture duration, i.e. maturation. Canagliflozin’s effects more pronounced than empagliflozin dapagliflozin. acutely altered Ca2+ handling Analyses SGLT2i-mediated mechanisms may underlie enhanced mutant excluded SGLT2, Na+/H+ exchanger, peak late Nav1.5 currents, L-type current, but indicate important role for Na+/Ca2+ exchanger. Indeed, electrophysiological measurements hiPSC-CM exchange current. Conclusion (canagliflozin &gt; dapagliflozin empagliflozin) EHT, especially upon prolonged culture.

Язык: Английский

Процитировано

12

Kidney outcomes in patients with diabetes mellitus did not differ between individual sodium-glucose cotransporter-2 inhibitors DOI Creative Commons
Yuta Suzuki, Hidehiro Kaneko, Akira Okada

и другие.

Kidney International, Год журнала: 2022, Номер 102(5), С. 1147 - 1153

Опубликована: Авг. 9, 2022

Язык: Английский

Процитировано

34

Comparative Cardiovascular Effectiveness of Empagliflozin Versus Dapagliflozin in Adults With Treated Type 2 Diabetes: A Target Trial Emulation DOI
Kasper Bonnesen, Uffe Heide‐Jørgensen, Diana Hedevang Christensen

и другие.

Circulation, Год журнала: 2024, Номер 150(18), С. 1401 - 1411

Опубликована: Авг. 29, 2024

BACKGROUND: Empagliflozin and dapagliflozin have proven cardiovascular benefits in people with type 2 diabetes at high risk, but their comparative effectiveness is unknown. METHODS: This study used nationwide, population-based Danish health registries to emulate a hypothetical target trial comparing empagliflozin versus initiation, addition standard care, among treated from 2014 through 2020. The outcome was composite of myocardial infarction, ischemic stroke, heart failure (HF), or death (major adverse event). Participants were followed until an outcome, emigration, occurred; 6 years after initiation; December 31, 2021, whichever occurred first. Logistic regression compute inverse probability treatment censoring weights, controlling for 57 potential confounders. In intention-to-treat analyses, 6-year adjusted risks, risk differences, ratios, considering noncardiovascular competing events, estimated. Analyses stratified by coexisting atherosclerotic disease HF. A per-protocol design performed as secondary analysis. RESULTS: There 36 670 eligible 20 606 initiators. the analysis, absolute major event not different between initiators (10.0% 10.0%; difference, 0.0% [95% CI, −0.9% 1.0%]; ratio, 1.00 0.91 1.11]). findings consistent (risk −2.3% −8.2% 3.5%]; 0.92 0.74 1.14]) without 0.3% −0.6% 1.2%]; 1.04 0.93 1.16]) HF 1.1% −6.5% 8.6%]; 0.79 1.37]) −0.1% −1.0% 0.8%]; 0.99 0.90 1.09]). risks also analysis (9.1% 8.8%; 0.2% −2.1% 2.5%]; 1.03 0.80 1.32]). CONCLUSIONS: had no differences outcomes adults

Язык: Английский

Процитировано

8