Microparticles as new markers of cardiovascular risk in diabetes and beyond
The term microparticle (MP) identifies a heterogeneous population of vesicles playing a relevant role in the pathogenesis of vascular diseases, cancer and metabolic diseases such as diabetes mellitus. MPs are released by virtually all cell types by shedding during cell growth, proliferation, activat...
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Published in | Thrombosis and haemostasis Vol. 116; no. 2; p. 220 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
01.08.2016
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Abstract | The term microparticle (MP) identifies a heterogeneous population of vesicles playing a relevant role in the pathogenesis of vascular diseases, cancer and metabolic diseases such as diabetes mellitus. MPs are released by virtually all cell types by shedding during cell growth, proliferation, activation, apoptosis or senescence processes. MPs, in particular platelet- and endothelial-derived MPs (PMPs and EMPs), are increased in a wide range of thrombotic disorders, with an interesting relationship between their levels and disease pathophysiology, activity or progression. EMP plasma levels have been associated with several cardiovascular diseases and risk factors. PMPs are also shown to be involved in the progressive formation of atherosclerotic plaque and development of arterial thrombosis, especially in diabetic patients. Indeed, diabetes is characterised by an increased procoagulant state and by a hyperreactive platelet phenotype, with enhanced adhesion, aggregation, and activation. Elevated MP levels, such as TF+ MPs, have been shown to be one of the procoagulant determinants in patients with type 2 diabetes mellitus. Atherosclerotic plaque constitutes an opulent source of sequestered MPs, called "plaque" MPs. Otherwise, circulating MPs represent a TF reservoir, named "blood-borne" TF, challenging the dogma that TF is a constitutive protein expressed in minute amounts. "Blood-borne" TF is mainly harboured by PMPs, and it can be trapped within the developing thrombus. MP detection and enumeration by polychromatic flow cytometry (PFC) have opened interesting perspectives in clinical settings, particularly for the evaluation of MP numbers and phenotypes as independent marker of cardiovascular risk, disease and outcome in diabetic patients. |
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AbstractList | The term microparticle (MP) identifies a heterogeneous population of vesicles playing a relevant role in the pathogenesis of vascular diseases, cancer and metabolic diseases such as diabetes mellitus. MPs are released by virtually all cell types by shedding during cell growth, proliferation, activation, apoptosis or senescence processes. MPs, in particular platelet- and endothelial-derived MPs (PMPs and EMPs), are increased in a wide range of thrombotic disorders, with an interesting relationship between their levels and disease pathophysiology, activity or progression. EMP plasma levels have been associated with several cardiovascular diseases and risk factors. PMPs are also shown to be involved in the progressive formation of atherosclerotic plaque and development of arterial thrombosis, especially in diabetic patients. Indeed, diabetes is characterised by an increased procoagulant state and by a hyperreactive platelet phenotype, with enhanced adhesion, aggregation, and activation. Elevated MP levels, such as TF+ MPs, have been shown to be one of the procoagulant determinants in patients with type 2 diabetes mellitus. Atherosclerotic plaque constitutes an opulent source of sequestered MPs, called "plaque" MPs. Otherwise, circulating MPs represent a TF reservoir, named "blood-borne" TF, challenging the dogma that TF is a constitutive protein expressed in minute amounts. "Blood-borne" TF is mainly harboured by PMPs, and it can be trapped within the developing thrombus. MP detection and enumeration by polychromatic flow cytometry (PFC) have opened interesting perspectives in clinical settings, particularly for the evaluation of MP numbers and phenotypes as independent marker of cardiovascular risk, disease and outcome in diabetic patients. |
Author | Miscia, Sebastiano Davì, Giovanni Santilli, Francesca Boccatonda, Andrea Lanuti, Paola Marchisio, Marco |
Author_xml | – sequence: 1 givenname: Francesca surname: Santilli fullname: Santilli, Francesca – sequence: 2 givenname: Marco surname: Marchisio fullname: Marchisio, Marco – sequence: 3 givenname: Paola surname: Lanuti fullname: Lanuti, Paola – sequence: 4 givenname: Andrea surname: Boccatonda fullname: Boccatonda, Andrea – sequence: 5 givenname: Sebastiano surname: Miscia fullname: Miscia, Sebastiano – sequence: 6 givenname: Giovanni surname: Davì fullname: Davì, Giovanni email: gdavi@unich.it organization: Prof. Giovanni Davì, Center of Excellence on Aging, "G. D'Annunzio" University Foundation, Via Colle dell'Ara, 66013 Chieti, Italy, Tel.: +39 0871 541312, Fax: +39 0871 541261, E-mail: gdavi@unich.it |
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SubjectTerms | Acute Coronary Syndrome - blood Acute Coronary Syndrome - etiology Atherosclerosis - blood Atherosclerosis - etiology Biomarkers - blood Blood Platelets - pathology Cardiovascular Diseases - blood Cardiovascular Diseases - etiology Cell-Derived Microparticles - pathology Diabetes Mellitus - blood Diabetes Mellitus, Type 2 - blood Diabetes Mellitus, Type 2 - complications Diabetic Cardiomyopathies - blood Diabetic Cardiomyopathies - etiology Endothelial Cells - pathology Humans Plaque, Atherosclerotic - blood Plaque, Atherosclerotic - etiology Risk Factors Stroke - blood Stroke - etiology Thromboplastin - metabolism |
Title | Microparticles as new markers of cardiovascular risk in diabetes and beyond |
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