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Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke

OBJECTIVE: It remains unclear when sufficient antiplatelet effect is achieved after administration of a loading dose of clopidogrel in patients with acute ischemic stroke (AIS). This study aimed to evaluate the clopidogrel response in patients with AIS identified by the platelet function test (PFT)....

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Autores principales: Enomoto, Yukiko, Shoda, Kenji, Mizutani, Daisuke, Matsubara, Hirofumi, Egashira, Yusuke, Iwama, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449631/
https://www.ncbi.nlm.nih.gov/pubmed/36090856
http://dx.doi.org/10.3389/fneur.2022.887243
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author Enomoto, Yukiko
Shoda, Kenji
Mizutani, Daisuke
Matsubara, Hirofumi
Egashira, Yusuke
Iwama, Toru
author_facet Enomoto, Yukiko
Shoda, Kenji
Mizutani, Daisuke
Matsubara, Hirofumi
Egashira, Yusuke
Iwama, Toru
author_sort Enomoto, Yukiko
collection PubMed
description OBJECTIVE: It remains unclear when sufficient antiplatelet effect is achieved after administration of a loading dose of clopidogrel in patients with acute ischemic stroke (AIS). This study aimed to evaluate the clopidogrel response in patients with AIS identified by the platelet function test (PFT). METHODS: P2Y(12) reaction unit (PRU) values measured using VerifyNow at baseline and at 6, 24, and 72 h after administration of a loading dose (300 mg) of clopidogrel were compared between patients with AIS and those of other cerebrovascular diseases (CVD). The prevalence of clopidogrel abnormal response and its associated factors were examined. RESULTS: The PRU value was significantly reduced with time in the other CVD group (p < 0.0001), and also in the AIS group (p = 0.0073). The PRU values were significantly higher in the AIS group than in the other CVD group (p < 0.0001 between the groups, baseline: 314 ± 53 vs. 284 ± 62, p = 0.35; 6 h: 290 ± 66 vs. 214 ± 71, p = 0.016; 24 h: 270 ± 75 vs. 190 ± 70, p < 0.0001; and 72 h: 231 ± 76 vs. 163 ± 93, p = 0.105). The prevalence of clopidogrel hypo-responder (PRU > 240 at 24 h after administration) was higher in the AIS group (79 vs. 33%, p < 0.0001) and associated with the baseline PRU value but not with the cytochrome P450 2C19 genotype or clinical ischemic events. CONCLUSIONS: Residual platelet reactivity at 24 h after clopidogrel loading was substantially higher in patients with AIS than in patients with other CVD. In addition, most patients with AIS were judged to be hypo-responders on PFT. This should be carefully interpreted in patients with AIS because of poor specificity for predicting clinical ischemic events.
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spelling pubmed-94496312022-09-08 Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke Enomoto, Yukiko Shoda, Kenji Mizutani, Daisuke Matsubara, Hirofumi Egashira, Yusuke Iwama, Toru Front Neurol Neurology OBJECTIVE: It remains unclear when sufficient antiplatelet effect is achieved after administration of a loading dose of clopidogrel in patients with acute ischemic stroke (AIS). This study aimed to evaluate the clopidogrel response in patients with AIS identified by the platelet function test (PFT). METHODS: P2Y(12) reaction unit (PRU) values measured using VerifyNow at baseline and at 6, 24, and 72 h after administration of a loading dose (300 mg) of clopidogrel were compared between patients with AIS and those of other cerebrovascular diseases (CVD). The prevalence of clopidogrel abnormal response and its associated factors were examined. RESULTS: The PRU value was significantly reduced with time in the other CVD group (p < 0.0001), and also in the AIS group (p = 0.0073). The PRU values were significantly higher in the AIS group than in the other CVD group (p < 0.0001 between the groups, baseline: 314 ± 53 vs. 284 ± 62, p = 0.35; 6 h: 290 ± 66 vs. 214 ± 71, p = 0.016; 24 h: 270 ± 75 vs. 190 ± 70, p < 0.0001; and 72 h: 231 ± 76 vs. 163 ± 93, p = 0.105). The prevalence of clopidogrel hypo-responder (PRU > 240 at 24 h after administration) was higher in the AIS group (79 vs. 33%, p < 0.0001) and associated with the baseline PRU value but not with the cytochrome P450 2C19 genotype or clinical ischemic events. CONCLUSIONS: Residual platelet reactivity at 24 h after clopidogrel loading was substantially higher in patients with AIS than in patients with other CVD. In addition, most patients with AIS were judged to be hypo-responders on PFT. This should be carefully interpreted in patients with AIS because of poor specificity for predicting clinical ischemic events. Frontiers Media S.A. 2022-08-24 /pmc/articles/PMC9449631/ /pubmed/36090856 http://dx.doi.org/10.3389/fneur.2022.887243 Text en Copyright © 2022 Enomoto, Shoda, Mizutani, Matsubara, Egashira and Iwama. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Enomoto, Yukiko
Shoda, Kenji
Mizutani, Daisuke
Matsubara, Hirofumi
Egashira, Yusuke
Iwama, Toru
Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title_full Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title_fullStr Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title_full_unstemmed Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title_short Platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
title_sort platelet reactivity after clopidogrel loading in patients with acute ischemic stroke
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449631/
https://www.ncbi.nlm.nih.gov/pubmed/36090856
http://dx.doi.org/10.3389/fneur.2022.887243
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