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Coagulation system activation and increase of D-dimer levels in peripheral arterial occlusive disease

✍ Scribed by M. De Buyzere; J. Philippé; Dr. D. Duprez; G. Baele; D. L. Clement


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
403 KB
Volume
43
Category
Article
ISSN
0361-8609

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✦ Synopsis


The aim of the present study was to document coagulation system activation and basal fibrinolysis in peripheral arterial occlusive disease (PAOD) at stage II of Fontaine's classification. In 34 patients, prothrombin fragment (F1 + 2), thrombin-antithrombin 111 complexes (TAT), and D-dimer concentrations were evaluated before and after a standard treadmill test. Basal levels in PAOD of F l + 2 (1.25 t 0.19 nrnol/liter) and of TAT (3.34 t 0.35 pglliter) were significantly increased compared to those obtained in age-and sex-matched healthy controls (0.68 t 0.06 nmol/liter and 2.30 2 0.33 pg/liter, respectively), showing baseline activation of the clotting cascade. A secondary activation of the fibrinolytic system was evidenced by the highly significant increase of basal D-dimers (719 t 99 ng/dl in PAOD vs. 229 t 37 ng/dl in controls). Treadmill exercise failed to increase the study parameters significantly further. Walking distance (583 5 40 m) was correlated with the preexercise ankle to brachial systolic blood pressure ratio (r = 0.485, P < 0.005) and inversely with the level of D-dirners (r = -0.425, P < 0.02). Under baseline conditions, the latter parameter was correlated as well with the antigen concentration of urokinase-type plasminogen activator (U-PA; r = 0.503, P < 0.002). These results indicate that stage II PAOD is characterized by an activation of the clotting cascade in baseline conditions evidenced by increased F1 + 2 and TAT. A secondary activation of the fibrinolytic system with increased U-PA antigen levels accounts for the elevated D-dimers. Treadmill exercise was unable to increase these parameters further.


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D-dimer and its relationship to fibrinog
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## Abstract Levels of D‐dimer and fibrinogen/fibrin degradation products (FDPs) are significantly elevated in patients with deep venous thrombosis, pulmonary embolism, disseminated intravascular coagulation, or other complications. The diagnosis of these disorders can be difficult, time‐consuming,