Extracellular vesicles number and cell subtype may be influenced by diabetes mellitus and metformin in patients at high cardiovascular risk

• Published in: Nutrition, metabolism, and cardiovascular diseases Vol. 33; no. 1; pp. 124 - 132
• Main Authors: Simeone, Paola G., Liani, Rossella, Bologna, Giuseppina, Tripaldi, Romina, Di Castelnuovo, Augusto, Simeone, Pasquale, D'Ardes, Damiano, Miscia, Sebastiano, Cipollone, Francesco, Marchisio, Marco, Consoli, Agostino, Lanuti, Paola, Santilli, Francesca
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.01.2023
• Subjects: Cardiovascular risk; Diabetes mellitus; Extracellular vesicles; Metformin; Vascular function; Extracellular vesicles; Metformin; Vascular function; Diabetes mellitus; Cardiovascular risk
• ISSN: 0939-4753; 1590-3729
• DOI: 10.1016/j.numecd.2022.09.010

Extracellular vesicles (EV) represent a population of small vesicles deriving from all types of cells, generated by the extroflection of the plasma membrane, and released into the circulation. EV can have both pro- and anti-atherothrombotic effects depending on the clinical setting, origin cell, stimuli, and different treatments might affect their levels. The primary endpoint of our study was to compare the amount of circulating EV and specific EV subtypes derived from platelets, endothelial cells, and leucocytes in subject at high CV risk, with and without T2DM, and if any ongoing anti-diabetic drugs could affect the levels of EV. The levels of total EV (d = 0.576; p = 0.049), total Annexin + EV (d = 0.519; p = 0.011), CD41a+/AnnexinV+ platelet derived EV (d = 0.482; p = 0.0187) and CD31 endothelial derived EV (d = 0.590; p = 0.0041) were lower in diabetic patients vs. those without T2DM. Interestingly, after adjustment for variables no significantly different between groups, including HbA1c, differences in EV subtypes were no longer observed. Linear regression analysis showed that HbA1c was inversely related to total EV to (beta coefficients = −10969; p = 0.0170), CD41a+/AnnexinV+ platelet-derived EV (beta coefficients = −352.71125; p = 0.0529) and CD31+ endothelial-derived EV (beta coefficients = −188.01952; p = 0.0095) in all patients. Among subjects with diabetes, CD41+ platelet-derived EV and CD41a+/AnnexinV+ platelet-derived EV (p = 0.0644 and p = 0.0635) were lower in patients on metformin treatment, even after adjustment for gender, hypertension, weight, waist circumference, total cholesterol, diuretics and statins use). Our study showed that, among high CV risk patients, treated with the state-of-the-art preventive strategies, T2DM is associated with lower levels of total, platelet-and endothelial-derived EV, and that this difference may be accounted for, at least in part, by hyperglycemia and ongoing treatment with metformin, the most widely prescribed oral antidiabetic agent. •Extracellular vesicles (EV) can have both pro- and anti-atherothrombotic effects.•DM is associated with lower levels of total, platelet-and endothelial-derived EV.•Platelet-derived AnnexinV + EV are lower in patients on treatment with metformin.•EV number may serve as biomarkers for the response to metformin intervention.