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Background: Sodium-glucose cotransporter 2 (SGLT2) inhibitors have demonstrated cardiovascular benefits in randomized trials. However, real-world evidence on their cardioprotective effect in high-risk populations with documented myocardial injury-such as heart failure (HF), acute coronary syndrome (ACS), myocardial revascularization, or cardiac surgery-is still limited.
Objective: To evaluate the impact of SGLT2 inhibitor adherence on cardiovascular outcomes in patients with type 2 diabetes mellitus (T2DM) and a history of myocardial injury, in a real-world setting.
Methods: We retrospectively reviewed the healthcare utilization databases of the Lombardy region (Italy) to identify all patients with T2DM who were dispensed SGLT2 inhibitors between 2014-2020, and had one hospitalization for HF, myocardial revascularization, ACS or cardiac surgery in the previous 10 years. Adherence was calculated as the proportion of days covered by therapy during follow-up. Cox regression analysis was performed to estimate the hazard ratios (HR) for cardiovascular hospitalizations and death.
Results: Among 1789 HF, 5759 revascularization, 3986 ACS, and 4580 cardiac surgery patients, higher adherence to SGLT2i therapy was consistently associated with a lower risk of CV events or death. Adjusted HRs for high vs. very low adherence were: HF, 0.65 (95 %CI:0.52-0.82); revascularization, 0.70 (95 %CI:0.59-0.84); ACS, 0.76 (95 %CI:0.62-0.93); and cardiac surgery, 0.69 (95 %CI:0.57-0.84). A dose-response trend was observed across adherence levels.
Conclusion: High adherence to SGLT2 inhibitors therapy can significantly decrease the risk of cardiovascular-related hospitalization and death in patients with T2DM and several forms of myocardial injury, such as HF, ACS, myocardial revascularization, and cardiac surgery.
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http://dx.doi.org/10.1016/j.hrtlng.2025.05.020 | DOI Listing |
J Prim Care Community Health
September 2025
Division of Nephrology, Department of Medicine, National University Hospital, Singapore.
Background: Chronic kidney disease (CKD) management was largely centered around renin-angiotensin-aldosterone system inhibitors (RAASi) optimization, until recent emergence of novel therapeutics. However, slow adoption of guideline-directed therapy leaves patients vulnerable to disease progression. In 2022, a data-driven informatics approach was introduced to track real-time adherence to best practices.
View Article and Find Full Text PDFInt Immunopharmacol
September 2025
Clinical Pharmacy Department, School of Pharmacy, Newgiza University, Giza, Egypt. Electronic address:
Ulcerative colitis (UC) is a persistent inflammatory condition marked by the destruction of the intestinal mucosal barrier, infiltration of inflammatory cells, and ulceration. M1/M2 macrophage polarization plays an imperative function in the regulation of inflammation through the nuclear factor-kappa B (NFκB) signaling pathway and modulating microRNA-155 (miR-155). Recent studies have highlighted the anti-ulcerogenic and colo-protective properties of sodium-glucose co-transporter-2 (SGLT2) inhibitors.
View Article and Find Full Text PDFHeart Lung Circ
September 2025
Lifelong Health Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia; Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia; Department of Cardiology, Central Adelaide Local Health Network, Adelaide, SA,
Cardiovascular-kidney-metabolic (CKM) syndrome is a term that is increasingly used to describe interconnected conditions that lead to poor health outcomes, including cardiovascular disease, chronic kidney disease, type 2 diabetes, and obesity. Historically, there have been very few targeted pharmacotherapies available that have changed cardiovascular outcomes for people with CKM syndromes; however, over the past decade, new pharmacologic options have rapidly expanded, with strong evidence for cardiovascular and kidney protective benefits in CKM conditions. Of note, sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists have emerged as key therapeutic options and are now widely guideline-endorsed.
View Article and Find Full Text PDFCell Regen
September 2025
Institute of Physical Chemistry, Polish Academy of Sciences, Warsaw, Poland.
Diabetes mellitus is a common and serious metabolic disease globally, characterized by increased blood glucose levels. The major pathogenesis is the functional impairment of insulin-producing beta cells in the pancreas and the lack of insulin secretion. Although both type 1 and type 2 diabetes develop through distinct pathological mechanisms, they lead to the destruction and/or dysfunction of beta cells, resulting in inadequate beta cell mass to maintain normal blood glucose levels.
View Article and Find Full Text PDFHeart Lung Circ
September 2025
Centre of Excellence for Cardiometabolic Health, Fiona Stanley Hospital, Perth, WA, Australia; Department of Cardiology, Fiona Stanley Hospital, Perth, WA, Australia; Medical School, The University of Western Australia, Perth, WA, Australia; Harry Perkins Institute of Medical Research, Perth, WA, Au
Background: In patients with type 2 diabetes (T2D) and chronic kidney disease (CKD), sodium-glucose cotransporter 2 (SGLT2) inhibitors, semaglutide (glucagon-like peptide-1 [GLP-1] agonist), and finerenone (non-steroidal mineralocorticoid receptor antagonist) improve renal and cardiovascular outcomes. We assessed real-world prescribing of these drugs in patients with T2D and CKD.
Method: The ReDiCare project retrospectively identified patients with T2D and CKD admitted to an Australian hospital between January 2020 and September 2024 using International Statistical Classification of Diseases and Related Health Problems 10th Revision Australian Modification codes.