The Sodium-Glucose Co-Transporter-2 (SGLT2) Inhibitors Reduce Platelet Activation and Thrombus Formation by Lowering NOX2-Related Oxidative Stress: A Pilot Study

• Published in: Antioxidants Vol. 11; no. 10; p. 1878
• Main Authors: Pignatelli, Pasquale, Baratta, Francesco, Buzzetti, Raffaella, D'Amico, Alessandra, Castellani, Valentina, Bartimoccia, Simona, Siena, Antonio, D'Onofrio, Luca, Maddaloni, Ernesto, Pingitore, Annachiara, Chiariello, Giovanni Alfonso, Santilli, Francesca, Pastori, Daniele, Cocomello, Nicholas, Violi, Francesco, Del Ben, Maria, Cammisotto, Vittoria, Carnevale, Roberto
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 22.09.2022; MDPI
• Subjects: Blood clots; Blood platelets; Collagen; CYBB protein; Diabetes; Diabetes mellitus (non-insulin dependent); Down-regulation; gliflozins; Glucose; Glucose metabolism; Glucose transporter; Heart failure; Hydrogen peroxide; Immunoassay; Ligands; Metformin; Mortality; Observations; Oxidants; Oxidative stress; Patients; platelet activation; Platelets; Thrombosis; type 2 diabetes; Values; United States; St Louis Missouri; United States > US; thrombosis; type 2 diabetes; gliflozins; oxidative stress; platelet activation
• ISSN: 2076-3921; 2076-3921
• DOI: 10.3390/antiox11101878

Sodium−glucose co-transporter-2 inhibitors or gliflozins, the newest anti-hyperglycemic class, induce cardioprotective benefits in patients with type 2 diabetes (T2D). As platelet activation and oxidative stress play a key role in atherothrombotic-related complications, we hypothesized that gliflozins might modulate oxidative stress, platelet activation and thrombus formation. We performed an interventional open-label single-arm before-after study in 32 T2D patients on top of their ongoing metformin therapy. The population was divided into two groups: treatment with GLP-1 receptor agonists (GLP-1RA, Group A) and gliflozins (Group B). Oxidative stress, platelet activation and thrombus growth were assessed before and after 15 days of treatment. Compared to the baseline, gliflozins treatment significantly decreased sNOX2-dp (−45.2%, p < 0.001), H2O2 production (−53.4%, p < 0.001), TxB2 (−33.1%, p < 0.001), sP-selectin (−49.3%, p < 0.001) and sCD40L levels (−62.3%, p < 0.001) as well as thrombus formation (−32%, p < 0.001), whereas it potentiated anti-oxidant power (HBA, +30.8%, p < 0.001). Moreover, a significant difference in oxidative stress, platelet activation and thrombus formation across groups A and B was found. In addition, an in vitro study on stimulated platelets treated with gliflozins (10−30 μM) showed a reduction in oxidative stress, platelet activation and thrombus growth. Our results showed that gliflozins have antiplatelet and antithrombic activity related to an NOX2 down-regulation, suggesting a new mechanism responsible for cardiovascular protection.