Early Increase of von Willebrand Factor Predicts Adverse Outcome in Unstable Coronary Artery Disease
| Autor: | Albert Dutoit, Annick Ankri, Alain Carayon, Daniel Thomas, Monique Chevrot, Didier Carrié, Daniel Flammang, Gilles Montalescot, Claude Jardel, Eric Vicaut, Fredérique Bigonzi, Jean Ernest Poulard, Jean Philippe Bastard, Etienne Bearez, François Philippe |
|---|---|
| Rok vydání: | 1998 |
| Předmět: |
medicine.medical_specialty
biology Unstable angina business.industry medicine.medical_treatment Heparin medicine.disease Revascularization Angina Coronary artery disease Von Willebrand factor Physiology (medical) Internal medicine Troponin I medicine biology.protein Cardiology Myocardial infarction Cardiology and Cardiovascular Medicine business medicine.drug |
| Zdroj: | Circulation. 98:294-299 |
| ISSN: | 1524-4539 0009-7322 |
| DOI: | 10.1161/01.cir.98.4.294 |
| Popis: | Background —The pathogenesis of unstable angina and non–Q-wave myocardial infarction is still poorly understood, and early evaluation of prognosis remains difficult. We therefore studied the predictive value of 5 biological indicators of inflammation, thrombogenesis, vasoconstriction, and myocardial necrosis, and we examined the effects of enoxaparin and unfractionated heparin on these markers after 48 hours of treatment. Methods and Results —Sixty-eight patients with unstable angina or non–Q-wave myocardial infarction randomized in the international ESSENCE trial participated in this French substudy. C-reactive protein, fibrinogen, von Willebrand factor antigen, endothelin-1 and troponin I were measured on admission and 48 hours later. The composite end point of death, myocardial infarction, recurrent angina, or revascularization was significantly lower at 14 and 30 days of follow-up in patients allocated to enoxaparin compared with unfractionated heparin. All acute-phase reactant proteins were elevated on admission and increased further at 48 hours. Multivariate analysis demonstrated that the rise of von Willebrand factor over 48 hours was a significant and independent predictor of the composite end point at both 14 days and 30 days. Moreover the early increase of von Willebrand factor was more frequent and more severe with unfractionated heparin than with enoxaparin (mean change was +8.7±8.8% with enoxaparin versus +93.9±11.7% with unfractionated heparin, P Conclusions —In patients with unstable angina or non–Q-wave myocardial infarction, the acute-phase proteins increase over the first 2 days despite medical treatment. The early rise of von Willebrand factor is an independent predictor of adverse clinical outcome at 14 days and at 30 days. Enoxaparin provides protection as evidenced by the reduced release of von Willebrand factor, which represents a favorable prognostic finding. |
| Databáze: | OpenAIRE |
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