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Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease
Background Patients with essential thrombocythemia (ET) and coronary artery disease (CAD) have increased risk of thromboembolic complications. In addition, a reduced antiplatelet effect of aspirin has been demonstrated in both patient groups. As ET is a platelet disorder, platelets may be more impo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255105/ https://www.ncbi.nlm.nih.gov/pubmed/34235392 http://dx.doi.org/10.1055/s-0041-1731309 |
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author | Pedersen, Oliver Buchhave Hvas, Anne-Mette Ommen, Hans Beier Kristensen, Steen Dalby Grove, Erik Lerkevang |
author_facet | Pedersen, Oliver Buchhave Hvas, Anne-Mette Ommen, Hans Beier Kristensen, Steen Dalby Grove, Erik Lerkevang |
author_sort | Pedersen, Oliver Buchhave |
collection | PubMed |
description | Background Patients with essential thrombocythemia (ET) and coronary artery disease (CAD) have increased risk of thromboembolic complications. In addition, a reduced antiplatelet effect of aspirin has been demonstrated in both patient groups. As ET is a platelet disorder, platelets may be more important for the thromboembolic risk in ET than in CAD. We aimed to investigate the antiplatelet effect of aspirin and platelet turnover in ET versus CAD patients. Methods We included 48 ET patients and an age-matched group of 48 CAD patients. The effect of aspirin was evaluated by thromboxane B (2) (TXB (2) ) levels and platelet aggregation. Platelet turnover was assessed by immature platelet count (IPC) and immature platelet fraction (IPF). Results ET patients had reduced effect of aspirin compared with CAD patients, demonstrated by significantly higher TXB (2) levels (median of differences = 22.3 ng/mL, p < 0.0001) and platelet aggregation (median of differences = 131.0 AU*min, p = 0.0003). Furthermore, ET patients had significantly higher IPC ( p < 0.0001) and IPF ( p = 0.0004) than CAD patients. Conclusion ET patients have lower 24-hour antiplatelet effect of aspirin than CAD patients. This may be explained by an increased platelet production and turnover counteracting the antiplatelet effect of aspirin. These findings strengthen the rationale for exploring novel antiplatelet regimens in ET patients to reduce the risk of cardiovascular events. |
format | Online Article Text |
id | pubmed-8255105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-82551052021-07-06 Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease Pedersen, Oliver Buchhave Hvas, Anne-Mette Ommen, Hans Beier Kristensen, Steen Dalby Grove, Erik Lerkevang TH Open Background Patients with essential thrombocythemia (ET) and coronary artery disease (CAD) have increased risk of thromboembolic complications. In addition, a reduced antiplatelet effect of aspirin has been demonstrated in both patient groups. As ET is a platelet disorder, platelets may be more important for the thromboembolic risk in ET than in CAD. We aimed to investigate the antiplatelet effect of aspirin and platelet turnover in ET versus CAD patients. Methods We included 48 ET patients and an age-matched group of 48 CAD patients. The effect of aspirin was evaluated by thromboxane B (2) (TXB (2) ) levels and platelet aggregation. Platelet turnover was assessed by immature platelet count (IPC) and immature platelet fraction (IPF). Results ET patients had reduced effect of aspirin compared with CAD patients, demonstrated by significantly higher TXB (2) levels (median of differences = 22.3 ng/mL, p < 0.0001) and platelet aggregation (median of differences = 131.0 AU*min, p = 0.0003). Furthermore, ET patients had significantly higher IPC ( p < 0.0001) and IPF ( p = 0.0004) than CAD patients. Conclusion ET patients have lower 24-hour antiplatelet effect of aspirin than CAD patients. This may be explained by an increased platelet production and turnover counteracting the antiplatelet effect of aspirin. These findings strengthen the rationale for exploring novel antiplatelet regimens in ET patients to reduce the risk of cardiovascular events. Georg Thieme Verlag KG 2021-07-04 /pmc/articles/PMC8255105/ /pubmed/34235392 http://dx.doi.org/10.1055/s-0041-1731309 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Pedersen, Oliver Buchhave Hvas, Anne-Mette Ommen, Hans Beier Kristensen, Steen Dalby Grove, Erik Lerkevang Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title | Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title_full | Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title_fullStr | Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title_full_unstemmed | Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title_short | Lower Antiplatelet Effect of Aspirin in Essential Thrombocythemia than in Coronary Artery Disease |
title_sort | lower antiplatelet effect of aspirin in essential thrombocythemia than in coronary artery disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255105/ https://www.ncbi.nlm.nih.gov/pubmed/34235392 http://dx.doi.org/10.1055/s-0041-1731309 |
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