Diabetic Microangiopathy: Lupus Anticoagulant Dependent Thrombotic Tendency in Type 1 (Insulin-dependent) Diabetes Mellitus
Type 1 (insulin‐dependent) diabetes mellitus is associated with long‐term vascular complications. In addition to metabolic factors, immunological and haemostatic mechanisms may be involved. Lupus anticoagulant (LA), an immunoglobulin which interferes with endothelial cell function, is frequently ass...
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Published in | Diabetic medicine Vol. 14; no. 2; pp. 132 - 137 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
01.02.1997
Blackwell |
Subjects | |
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Abstract | Type 1 (insulin‐dependent) diabetes mellitus is associated with long‐term vascular complications. In addition to metabolic factors, immunological and haemostatic mechanisms may be involved. Lupus anticoagulant (LA), an immunoglobulin which interferes with endothelial cell function, is frequently associated with a high risk of thromboembolic events. LA has been described in several diseases but never in diabetes mellitus. The aim of this study was to evaluate if endothelial dysfunction and unmodulated haemostasis are amplified by the presence of LA in Type 1 diabetic patients. Plasma samples collected from clinically and biochemically well‐characterized Type 1 diabetic patients were examined for LA, fibrinogen, prothrombin (PT), PTT, prothrombin degradation products (F1 + 2) and activated protein C (APC). The results revealed significantly decreased APC and increased F1 + 2 plasma concentrations in LA‐positive but not in LA‐negative patients; 60 % of LA‐positive and only 18 % of LA‐negative patients had microangiopathy (not significant). No thrombotic episodes in large vessels were found in LA‐positive patients. These findings suggest that LA could be considered an additional factor in the onset and/or progression of diabetic complications, acting as a link between the immunological and haemostatic systems in the pathogenesis of diabetic microangiopathy. © 1997 by John Wiley & Sons, Ltd. |
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AbstractList | Type 1 (insulin-dependent) diabetes mellitus is associated with long-term vascular complications. In addition to metabolic factors, immunological and haemostatic mechanisms may be involved. Lupus anticoagulant (LA), an immunoglobulin which interferes with endothelial cell function, is frequently associated with a high risk of thromboembolic events. LA has been described in several diseases but never in diabetes mellitus. The aim of this study was to evaluate if endothelial dysfunction and unmodulated haemostasis are amplified by the presence of LA in Type 1 diabetic patients. Plasma samples collected from clinically and biochemically well-characterized Type 1 diabetic patients were examined for LA, fibrinogen, prothrombin (PT), PTT, prothrombin degradation products (F1 + 2) and activated protein C (APC). The results revealed significantly decreased APC and increased F1 + 2 plasma concentrations in LA-positive but not in LA-negative patients; 60% of LA-positive and only 18% of LA-negative patients had microangiopathy (not significant). No thrombotic episodes in large vessels were found in LA-positive patients. These findings suggest that LA could be considered an additional factor in the onset and/or progression of diabetic complications, acting as a link between the immunological and haemostatic systems in the pathogenesis of diabetic microangiopathy. Type 1 (insulin‐dependent) diabetes mellitus is associated with long‐term vascular complications. In addition to metabolic factors, immunological and haemostatic mechanisms may be involved. Lupus anticoagulant (LA), an immunoglobulin which interferes with endothelial cell function, is frequently associated with a high risk of thromboembolic events. LA has been described in several diseases but never in diabetes mellitus. The aim of this study was to evaluate if endothelial dysfunction and unmodulated haemostasis are amplified by the presence of LA in Type 1 diabetic patients. Plasma samples collected from clinically and biochemically well‐characterized Type 1 diabetic patients were examined for LA, fibrinogen, prothrombin (PT), PTT, prothrombin degradation products (F1 + 2) and activated protein C (APC). The results revealed significantly decreased APC and increased F1 + 2 plasma concentrations in LA‐positive but not in LA‐negative patients; 60 % of LA‐positive and only 18 % of LA‐negative patients had microangiopathy (not significant). No thrombotic episodes in large vessels were found in LA‐positive patients. These findings suggest that LA could be considered an additional factor in the onset and/or progression of diabetic complications, acting as a link between the immunological and haemostatic systems in the pathogenesis of diabetic microangiopathy. © 1997 by John Wiley & Sons, Ltd. |
Author | Bosco, D. Pantaleo, A. Arcieri, P. Gargiulo, P. Ciampalini, P. Romani, B. Andreani, D. Schiaffini, R. |
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Keywords | Endocrinopathy Human Immunopathology Endothelial cell Immunoglobulins Circulating anticoagulant Cell function Pathogenesis Cardiovascular disease Autoimmune disease Vascular disease Microangiopathy Hemostasis Insulin dependent diabetes Complication Thromboembolism |
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SubjectTerms | Adult Aged Associated diseases and complications Biological and medical sciences Blood Coagulation Blood Pressure Body Mass Index Creatinine - blood Diabetes Mellitus, Type 1 - blood Diabetes Mellitus, Type 1 - complications Diabetes Mellitus, Type 1 - physiopathology Diabetes. Impaired glucose tolerance Diabetic Angiopathies - etiology Diabetic Angiopathies - physiopathology Diabetic microangiopathy Diabetic Nephropathies - etiology Diabetic Retinopathy - etiology Endocrine pancreas. Apud cells (diseases) Endocrinopathies Endothelial cell dysfunction Female Fibrinogen - metabolism Haemostatic system Humans Lupus anticoagulant Lupus Coagulation Inhibitor - blood Male Medical sciences Middle Aged Thrombosis - blood Thrombosis - complications Type 1 diabetes mellitus |
Title | Diabetic Microangiopathy: Lupus Anticoagulant Dependent Thrombotic Tendency in Type 1 (Insulin-dependent) Diabetes Mellitus |
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