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Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia

Patients with essential thrombocythaemia (ET) have an increased risk of thromboembolic events, which may differ according to different cytoreductive drugs. We investigated the effect of cytoreductive treatment on platelet function and turnover in ET patients. Blood samples were obtained at 1 and 24 ...

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Autores principales: Pedersen, Oliver Buchhave, Grove, Erik Lerkevang, Pasalic, Leonardo, Ommen, Hans Beier, Kristensen, Steen Dalby, Hvas, Anne‐Mette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540443/
https://www.ncbi.nlm.nih.gov/pubmed/35675970
http://dx.doi.org/10.1111/bjh.18303
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author Pedersen, Oliver Buchhave
Grove, Erik Lerkevang
Pasalic, Leonardo
Ommen, Hans Beier
Kristensen, Steen Dalby
Hvas, Anne‐Mette
author_facet Pedersen, Oliver Buchhave
Grove, Erik Lerkevang
Pasalic, Leonardo
Ommen, Hans Beier
Kristensen, Steen Dalby
Hvas, Anne‐Mette
author_sort Pedersen, Oliver Buchhave
collection PubMed
description Patients with essential thrombocythaemia (ET) have an increased risk of thromboembolic events, which may differ according to different cytoreductive drugs. We investigated the effect of cytoreductive treatment on platelet function and turnover in ET patients. Blood samples were obtained at 1 and 24 h after aspirin intake. Platelet function was evaluated by platelet aggregation and flow cytometry. Platelet turnover was assessed by immature platelet count, immature platelet fraction (IPF) and mean platelet volume (MPV). A total of 47 ET patients were included and grouped into 21 patients not receiving cytoreductive treatment, 15 patients receiving hydroxycarbamide and 11 patients receiving pegylated interferon alpha (peg‐IFN). Patients receiving peg‐IFN had significantly higher IPF and MPV than the other ET groups. Patients not receiving cytoreductive treatment had significantly higher platelet aggregation 24 h after aspirin intake than the other ET groups (p‐values from 0.03 to 0.0002). Patients receiving hydroxycarbamide had significantly higher expression of platelet granule makers, P‐selectin and CD63, than patients receiving peg‐IFN (p‐values ≤0.003). Cytoreduction provides more consistent platelet inhibition compared with no cytoreductive treatment. Moreover, peg‐IFN provides superior inhibition of platelet activation markers than hydroxycarbamide, which in part may explain differences in risk of thromboembolic events in ET patients.
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spelling pubmed-95404432022-10-14 Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia Pedersen, Oliver Buchhave Grove, Erik Lerkevang Pasalic, Leonardo Ommen, Hans Beier Kristensen, Steen Dalby Hvas, Anne‐Mette Br J Haematol Haematological Malignancy–Clinical Patients with essential thrombocythaemia (ET) have an increased risk of thromboembolic events, which may differ according to different cytoreductive drugs. We investigated the effect of cytoreductive treatment on platelet function and turnover in ET patients. Blood samples were obtained at 1 and 24 h after aspirin intake. Platelet function was evaluated by platelet aggregation and flow cytometry. Platelet turnover was assessed by immature platelet count, immature platelet fraction (IPF) and mean platelet volume (MPV). A total of 47 ET patients were included and grouped into 21 patients not receiving cytoreductive treatment, 15 patients receiving hydroxycarbamide and 11 patients receiving pegylated interferon alpha (peg‐IFN). Patients receiving peg‐IFN had significantly higher IPF and MPV than the other ET groups. Patients not receiving cytoreductive treatment had significantly higher platelet aggregation 24 h after aspirin intake than the other ET groups (p‐values from 0.03 to 0.0002). Patients receiving hydroxycarbamide had significantly higher expression of platelet granule makers, P‐selectin and CD63, than patients receiving peg‐IFN (p‐values ≤0.003). Cytoreduction provides more consistent platelet inhibition compared with no cytoreductive treatment. Moreover, peg‐IFN provides superior inhibition of platelet activation markers than hydroxycarbamide, which in part may explain differences in risk of thromboembolic events in ET patients. John Wiley and Sons Inc. 2022-06-08 2022-08 /pmc/articles/PMC9540443/ /pubmed/35675970 http://dx.doi.org/10.1111/bjh.18303 Text en © 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Haematological Malignancy–Clinical
Pedersen, Oliver Buchhave
Grove, Erik Lerkevang
Pasalic, Leonardo
Ommen, Hans Beier
Kristensen, Steen Dalby
Hvas, Anne‐Mette
Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title_full Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title_fullStr Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title_full_unstemmed Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title_short Cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
title_sort cytoreductive treatment and association with platelet function and maturity in patients with essential thrombocythaemia
topic Haematological Malignancy–Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540443/
https://www.ncbi.nlm.nih.gov/pubmed/35675970
http://dx.doi.org/10.1111/bjh.18303
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