Impaired spontaneous/endogenous fibrinolytic status as new cardiovascular risk factor? JACC Review Topic of the Week
File(s)Review Topic of the Week 10.06.19.pdf (310.65 KB)
Accepted version
Author(s)
Gorog, Diana A
Lip, Gregory YH
Type
Journal Article
Abstract
Endogenous fibrinolysis is a powerful natural defence mechanism against lasting arterial
thrombotic occlusion. Recent prospective studies show that impaired endogenous fibrinolysis
(or hypofibrinolysis) can be detected in a significant number of patients with acute coronary
syndrome (ACS) using global assays and is a strong marker of future cardiovascular risk.
This novel risk biomarker is independent of traditional cardiovascular risk factors and
unaffected by antiplatelet therapy. Nevertheless, the optimal test to assess endogenous
fibrinolysis is not clear. Most prospective, prognostic data have been obtained using a global
assay employing native whole blood at high shear or plasma turbidimetric assays.
For example, tests of endogenous fibrinolysis could be used to identify ACS patients who,
despite antiplatelet therapy, remain at high cardiovascular risk. Clinical trials of
pharmacotherapy to favourably modulate fibrinolytic status are required as a potential new
avenue to improve outcomes in ACS.
thrombotic occlusion. Recent prospective studies show that impaired endogenous fibrinolysis
(or hypofibrinolysis) can be detected in a significant number of patients with acute coronary
syndrome (ACS) using global assays and is a strong marker of future cardiovascular risk.
This novel risk biomarker is independent of traditional cardiovascular risk factors and
unaffected by antiplatelet therapy. Nevertheless, the optimal test to assess endogenous
fibrinolysis is not clear. Most prospective, prognostic data have been obtained using a global
assay employing native whole blood at high shear or plasma turbidimetric assays.
For example, tests of endogenous fibrinolysis could be used to identify ACS patients who,
despite antiplatelet therapy, remain at high cardiovascular risk. Clinical trials of
pharmacotherapy to favourably modulate fibrinolytic status are required as a potential new
avenue to improve outcomes in ACS.
Date Issued
2019-09
Date Acceptance
2019-07-19
Citation
Journal of the American College of Cardiology, 2019, 74 (10), pp.1366-1375
ISSN
0735-1097
Publisher
Elsevier BV
Start Page
1366
End Page
1375
Journal / Book Title
Journal of the American College of Cardiology
Volume
74
Issue
10
Copyright Statement
© 2019 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/
Identifier
https://www.sciencedirect.com/science/article/pii/S0735109719359613?via%3Dihub
Subjects
1102 Cardiorespiratory Medicine and Haematology
1117 Public Health and Health Services
Cardiovascular System & Hematology
Publication Status
Published
Date Publish Online
2019-09-02