D-dimer predicts major bleeding, cardiovascular events and all-cause mortality during warfarin treatment Visa övriga samt affilieringar
2014 (Engelska) Ingår i: Clinical Biochemistry, ISSN 0009-9120, E-ISSN 1873-2933, Vol. 47, nr 7-8, s. 570-573Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Objectives: Previous studies have shown that biomarkers in blood plasma can predict bleeding complications during anticoagulant treatment as well as thromboembolic events and may improve existing risk stratification schemes in patients on or considered for oral anticoagulant treatment. The aim of this study was to investigate if levels of D-dimer, tissue plasminogen activator (tPA) and its complex with plasminogen inhibitor type 1 (tPA/PAI-1 complex) can predict major bleedings, cardiovascular events and all-cause mortality in patients with warfarin treatment.
Design and methods: In a longitudinal cohort study, 719 patients on oral anticoagulant treatment were followed for a total of 3001 treatment years. Major bleeding, stroke, arterial emboli, myocardial infarction and death were recorded and classified. Blood samples collected at baseline were analyzed for D-dimer, tPA, and tPA/PAI-1 complex.
Results: In multivariate Cox regression analysis, high levels of D-dimer were associated with major bleeding (HR 1.27 per SD; 95% CI: 1.01-1.60), cardiovascular events (HR 1.23 per SD; 95% CI: 1.05-1.45) and all-cause mortality (HR 1.25 per SD; 95% CI: 1.06-1.47). Neither tPA nor the tPA/PAI-1 complex was associated with major bleeding, cardiovascular events or all-cause mortality.
Conclusion: We conclude that high levels of D-dimer predict major bleeding, cardiovascular events and all-cause mortality during warfarin treatment. (C) 2014 The Canadian Society of Clinical Chemists.
Ort, förlag, år, upplaga, sidor 2014. Vol. 47, nr 7-8, s. 570-573
Nyckelord [en]
D-dimer, Bleeding, Warfarin, Mortality, PAI-1, Cardiovascular events
Nationell ämneskategori
Kardiologi och kardiovaskulära sjukdomar
Identifikatorer URN: urn:nbn:se:umu:diva-90777 DOI: 10.1016/j.clinbiochem.2014.03.003 ISI: 000335905200012 PubMedID: 24636802 Scopus ID: 2-s2.0-84900307939 OAI: oai:DiVA.org:umu-90777 DiVA, id: diva2:754326
2014-10-102014-07-012025-02-10 Bibliografiskt granskad