The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker

Abstract Atrial fibrillation (AF) is a major risk factor for stroke. We aim to characterize AF patients and the effects of apixaban therapy in terms of clot microstructure using gel point analysis, a novel biomarker. Seventy‐eight patients were included in the study, 50 Stroke with AF (AF‐S), and 28...

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Main Authors: Matthew J. Lawrence, Vanessa Evans, Janet Whitley, Suresh Pillai, Phylip R. Williams, James Coulson, Manju Krishnan, Peter Slade, Kieron Power, Roger H.K. Morris, Phillip A. Evans
Format: Article
Language:English
Published: Wiley 2022-04-01
Series:Pharmacology Research & Perspectives
Subjects:
Online Access:https://doi.org/10.1002/prp2.937
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author Matthew J. Lawrence
Vanessa Evans
Janet Whitley
Suresh Pillai
Phylip R. Williams
James Coulson
Manju Krishnan
Peter Slade
Kieron Power
Roger H.K. Morris
Phillip A. Evans
author_facet Matthew J. Lawrence
Vanessa Evans
Janet Whitley
Suresh Pillai
Phylip R. Williams
James Coulson
Manju Krishnan
Peter Slade
Kieron Power
Roger H.K. Morris
Phillip A. Evans
author_sort Matthew J. Lawrence
collection DOAJ
description Abstract Atrial fibrillation (AF) is a major risk factor for stroke. We aim to characterize AF patients and the effects of apixaban therapy in terms of clot microstructure using gel point analysis, a novel biomarker. Seventy‐eight patients were included in the study, 50 Stroke with AF (AF‐S), and 28 AF without stroke (AF). Pre‐ and post‐anticoagulation samples were collected: gel point (GP) analysis was performed to obtain (i) TGP (the time taken to reach the GP or the clot formation time) and (ii) df, the fractal dimension of the clot, a quantification of clot fibrin microstructure at the GP. At baseline, the AF‐S group had a df = 1.70 (±0.05) and TGP = 306 (±73 s). The AF group had a df = 1.70 ± 0.05 and TGP = 346 ± 78 s, showing a significantly shortened TGP in the stroke group (p = .008). For both groups, apixaban significantly prolonged TGP, p = .005, but resulted in no change in df. Apixaban prolonged clotting time while having no significant impact on the blood’s ability to form stable clots (no change in df). This indicates that apixaban provides protection from the formation of thrombi by reducing clotting kinetics.
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spelling doaj.art-a20d7bd65b524b57863155638c0a89f52022-12-22T01:21:30ZengWileyPharmacology Research & Perspectives2052-17072022-04-01102n/an/a10.1002/prp2.937The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarkerMatthew J. Lawrence0Vanessa Evans1Janet Whitley2Suresh Pillai3Phylip R. Williams4James Coulson5Manju Krishnan6Peter Slade7Kieron Power8Roger H.K. Morris9Phillip A. Evans10Welsh Centre for Emergency Medicine Research Swansea Bay University Health Board Swansea UKWelsh Centre for Emergency Medicine Research Swansea Bay University Health Board Swansea UKWelsh Centre for Emergency Medicine Research Swansea Bay University Health Board Swansea UKWelsh Centre for Emergency Medicine Research Swansea Bay University Health Board Swansea UKCollege of Engineering Swansea University Swansea UKSchool of Medicine Cardiff University Cardiff UKStroke Unit Swansea Bay University Health Board Swansea UKStroke Unit Swansea Bay University Health Board Swansea UKPharmacy Department Swansea Bay University Health Board Swansea UKSchool of Applied Science Cardiff Metropolitan University Cardiff UKWelsh Centre for Emergency Medicine Research Swansea Bay University Health Board Swansea UKAbstract Atrial fibrillation (AF) is a major risk factor for stroke. We aim to characterize AF patients and the effects of apixaban therapy in terms of clot microstructure using gel point analysis, a novel biomarker. Seventy‐eight patients were included in the study, 50 Stroke with AF (AF‐S), and 28 AF without stroke (AF). Pre‐ and post‐anticoagulation samples were collected: gel point (GP) analysis was performed to obtain (i) TGP (the time taken to reach the GP or the clot formation time) and (ii) df, the fractal dimension of the clot, a quantification of clot fibrin microstructure at the GP. At baseline, the AF‐S group had a df = 1.70 (±0.05) and TGP = 306 (±73 s). The AF group had a df = 1.70 ± 0.05 and TGP = 346 ± 78 s, showing a significantly shortened TGP in the stroke group (p = .008). For both groups, apixaban significantly prolonged TGP, p = .005, but resulted in no change in df. Apixaban prolonged clotting time while having no significant impact on the blood’s ability to form stable clots (no change in df). This indicates that apixaban provides protection from the formation of thrombi by reducing clotting kinetics.https://doi.org/10.1002/prp2.937anticoagulationapixabancerebrovascular diseaseclot microstructuregel point and fractal analysis
spellingShingle Matthew J. Lawrence
Vanessa Evans
Janet Whitley
Suresh Pillai
Phylip R. Williams
James Coulson
Manju Krishnan
Peter Slade
Kieron Power
Roger H.K. Morris
Phillip A. Evans
The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
Pharmacology Research & Perspectives
anticoagulation
apixaban
cerebrovascular disease
clot microstructure
gel point and fractal analysis
title The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
title_full The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
title_fullStr The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
title_full_unstemmed The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
title_short The effects of apixaban on clot characteristics in atrial fibrillation: A novel pharmacodynamic biomarker
title_sort effects of apixaban on clot characteristics in atrial fibrillation a novel pharmacodynamic biomarker
topic anticoagulation
apixaban
cerebrovascular disease
clot microstructure
gel point and fractal analysis
url https://doi.org/10.1002/prp2.937
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