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Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors

BACKGROUND: Gender influences platelet biology. Women have a larger platelet count, but gender-based differences in platelet function remain debated. We performed a study addressing gender-based differences in platelet function using point-of-care platelet function tests (PFT). METHODS: The patient...

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Autores principales: Ranucci, Marco, Aloisio, Tommaso, Di Dedda, Umberto, Menicanti, Lorenzo, de Vincentiis, Carlo, Baryshnikova, Ekaterina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881030/
https://www.ncbi.nlm.nih.gov/pubmed/31774869
http://dx.doi.org/10.1371/journal.pone.0225771
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author Ranucci, Marco
Aloisio, Tommaso
Di Dedda, Umberto
Menicanti, Lorenzo
de Vincentiis, Carlo
Baryshnikova, Ekaterina
author_facet Ranucci, Marco
Aloisio, Tommaso
Di Dedda, Umberto
Menicanti, Lorenzo
de Vincentiis, Carlo
Baryshnikova, Ekaterina
author_sort Ranucci, Marco
collection PubMed
description BACKGROUND: Gender influences platelet biology. Women have a larger platelet count, but gender-based differences in platelet function remain debated. We performed a study addressing gender-based differences in platelet function using point-of-care platelet function tests (PFT). METHODS: The patient population consisted of 760 cardiac surgery patients where preoperative PFT (multiple-electrode aggregometry [MEA]) were available. Platelet count and function at the ADPtest and TRAPtest were compared in the overall population and separately in patients with or without residual effects of P2Y(12) inhibitors. RESULTS: Women had a significantly (P = 0.001) higher platelet count but a non-significantly higher platelet reactivity to ADP. In clopidogrel-treated patients, the platelets ADP reactivity was significantly (P = 0.031) higher in women, and platelet count was the main determinant of platelet hyper-reactivity. Within patients under full clopidogrel effects, women with a platelet count ≥ 200,000 cells/μL had a significantly (P = 0.023) higher rate of high-on-treatment platelet reactivity (HTPR, 45.5%) with respect to males with a platelet count < 200,000 cells/μL (11.9%), with a relative risk of 6.2 (95% confidence interval 1.4–29). CONCLUSIONS: Our findings confirm that women have a larger platelet count than men, and that this is associated to a trend towards a higher platelet reactivity. HTPR is largely represented in women with a high platelet count. This generates the hypothesis that women requiring P2Y(12) inhibitors could potentially benefit from larger doses of drug or should be treated with anti-platelet agents with a low rate of HTPR.
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spelling pubmed-68810302019-12-08 Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors Ranucci, Marco Aloisio, Tommaso Di Dedda, Umberto Menicanti, Lorenzo de Vincentiis, Carlo Baryshnikova, Ekaterina PLoS One Research Article BACKGROUND: Gender influences platelet biology. Women have a larger platelet count, but gender-based differences in platelet function remain debated. We performed a study addressing gender-based differences in platelet function using point-of-care platelet function tests (PFT). METHODS: The patient population consisted of 760 cardiac surgery patients where preoperative PFT (multiple-electrode aggregometry [MEA]) were available. Platelet count and function at the ADPtest and TRAPtest were compared in the overall population and separately in patients with or without residual effects of P2Y(12) inhibitors. RESULTS: Women had a significantly (P = 0.001) higher platelet count but a non-significantly higher platelet reactivity to ADP. In clopidogrel-treated patients, the platelets ADP reactivity was significantly (P = 0.031) higher in women, and platelet count was the main determinant of platelet hyper-reactivity. Within patients under full clopidogrel effects, women with a platelet count ≥ 200,000 cells/μL had a significantly (P = 0.023) higher rate of high-on-treatment platelet reactivity (HTPR, 45.5%) with respect to males with a platelet count < 200,000 cells/μL (11.9%), with a relative risk of 6.2 (95% confidence interval 1.4–29). CONCLUSIONS: Our findings confirm that women have a larger platelet count than men, and that this is associated to a trend towards a higher platelet reactivity. HTPR is largely represented in women with a high platelet count. This generates the hypothesis that women requiring P2Y(12) inhibitors could potentially benefit from larger doses of drug or should be treated with anti-platelet agents with a low rate of HTPR. Public Library of Science 2019-11-27 /pmc/articles/PMC6881030/ /pubmed/31774869 http://dx.doi.org/10.1371/journal.pone.0225771 Text en © 2019 Ranucci et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ranucci, Marco
Aloisio, Tommaso
Di Dedda, Umberto
Menicanti, Lorenzo
de Vincentiis, Carlo
Baryshnikova, Ekaterina
Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title_full Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title_fullStr Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title_full_unstemmed Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title_short Gender-based differences in platelet function and platelet reactivity to P2Y(12) inhibitors
title_sort gender-based differences in platelet function and platelet reactivity to p2y(12) inhibitors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881030/
https://www.ncbi.nlm.nih.gov/pubmed/31774869
http://dx.doi.org/10.1371/journal.pone.0225771
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