Prothrombin fragment 1+2 and thrombin???antithrombin III complex as markers of activation of blood coagulation in inflammatory bowel diseases

التفاصيل البيبلوغرافية
العنوان: Prothrombin fragment 1+2 and thrombin???antithrombin III complex as markers of activation of blood coagulation in inflammatory bowel diseases
المؤلفون: Marie-Louise Wiesel, Pierre Louis Frey, Christian Wittersheim, René Baumann, P. Chamouard, René Sapin, Jean-Pierre Cazenave, Lelia Grunebaum
المصدر: European Journal of Gastroenterology & Hepatology. 12:1183-1188
بيانات النشر: Ovid Technologies (Wolters Kluwer Health), 1995.
سنة النشر: 1995
مصطلحات موضوعية: Adult, Male, Pancolitis, medicine.medical_specialty, Adolescent, Thrombomodulin, Antithrombin III, Gastroenterology, Pathogenesis, Crohn Disease, Internal medicine, Humans, Medicine, Colitis, Blood Coagulation, Aged, Aged, 80 and over, Hepatology, biology, Tumor Necrosis Factor-alpha, business.industry, PROTHROMBIN FRAGMENT 1.2, Inflammatory Bowel Diseases, Thrombosis, Middle Aged, medicine.disease, Ulcerative colitis, Peptide Fragments, C-Reactive Protein, Coagulation, Antibodies, Anticardiolipin, Immunology, biology.protein, Colitis, Ulcerative, Female, Prothrombin, medicine.symptom, Antibody, business, Biomarkers, Peptide Hydrolases, circulatory and respiratory physiology
الوصف: OBJECTIVES AND METHODS The aims of the present work were to assess the presence of thrombin generation in Crohn's disease and in ulcerative colitis by using the prothrombin fragment 1 + 2 and the thrombin-antithrombin III complex assays and to study the possible relationships between these markers and disease activity. RESULTS Prothrombin fragment 1 + 2 and thrombin-antithrombin III complex were significantly raised in patients with Crohn's disease (n = 69) and with ulcerative colitis (n = 25) as compared with healthy controls (n = 50). In Crohn's disease these two markers of thrombin generation were correlated with the Van Hees index (P < 0.05 and P < 0.001, respectively); values were significantly different from controls even in the patient group displaying the lowest disease activity (P < 0.001). No correlation was found with tumour necrosis factor alpha and C-reactive protein; nevertheless patients with C-reactive protein less than or equal to 10 mg/l had significant lower values of prothrombin fragment 1 + 2 (P < 0.03). In ulcerative colitis prothrombin fragment 1 + 2 and thrombin-antithrombin III complex were significantly increased by comparison with controls, were higher in patients with pancolitis and correlated with C-reactive protein (P < 0.002 and P < 0.009, respectively). CONCLUSION These data show that prothrombin fragment 1 + 2 and thrombin-antithrombin III complex are increased in inflammatory bowel diseases and suggest that thrombin generation might be an early event in their pathogenesis.
تدمد: 0954-691X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21faf679de0949e6bb7f8f9db0ec1614Test
https://doi.org/10.1097/00042737-199512000-00010Test
رقم الانضمام: edsair.doi.dedup.....21faf679de0949e6bb7f8f9db0ec1614
قاعدة البيانات: OpenAIRE