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TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study

INTRODUCTION: This prospective study aimed to determine whether trimetazidine (TMZ) alters the pharmacodynamic (PD) effects of clopidogrel. METHODS: Patients with stable coronary artery disease (SCAD) (n = 24) who were actively treated with dual antiplatelet therapy (DAPT) of aspirin 81 mg daily and...

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Autores principales: Seecheran, Naveen, Seebalack, Victoria, Seecheran, Rajeev, Maharaj, Aarti, Boodhai, Brent, Seecheran, Valmiki, Persad, Sangeeta, Motilal, Shastri, Tello-Montoliu, Antonio, Schneider, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828882/
https://www.ncbi.nlm.nih.gov/pubmed/31292901
http://dx.doi.org/10.1007/s40119-019-0139-0
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author Seecheran, Naveen
Seebalack, Victoria
Seecheran, Rajeev
Maharaj, Aarti
Boodhai, Brent
Seecheran, Valmiki
Persad, Sangeeta
Motilal, Shastri
Tello-Montoliu, Antonio
Schneider, David
author_facet Seecheran, Naveen
Seebalack, Victoria
Seecheran, Rajeev
Maharaj, Aarti
Boodhai, Brent
Seecheran, Valmiki
Persad, Sangeeta
Motilal, Shastri
Tello-Montoliu, Antonio
Schneider, David
author_sort Seecheran, Naveen
collection PubMed
description INTRODUCTION: This prospective study aimed to determine whether trimetazidine (TMZ) alters the pharmacodynamic (PD) effects of clopidogrel. METHODS: Patients with stable coronary artery disease (SCAD) (n = 24) who were actively treated with dual antiplatelet therapy (DAPT) of aspirin 81 mg daily and clopidogrel 75 mg daily were recruited. Platelet function was measured with the VerifyNow P2Y12 assay (Accriva Diagnostics, San Diego, CA, USA) and assessed before the initiation of and after 14 days of treatment with TMZ. Results were compared using a paired t test. RESULTS: Almost 80% of the study population were of South Asian descent and had diabetes mellitus (DM). P2Y12 reaction units (PRUs) were higher in patients on TMZ (204 ± 56 compared with 174 ± 71 before TMZ, p = 0.005). The average increase in PRU score was 29 (95% confidence interval 8.8–49.7). Before TMZ, the proportion of patients with high on-treatment platelet reactivity (PRU > 208 units) was 25%, which increased to 42% for patients on TMZ. CONCLUSION: Higher platelet reactivity was seen in patients on TMZ, suggesting that TMZ attenuated the PD effects of clopidogrel in this study of a predominantly South Asian diabetic subpopulation. Alternative therapies should be considered and further research is warranted. TRIAL REGISTRATION: ClinicalTrials.gov number, NCT03603249.
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spelling pubmed-68288822019-11-18 TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study Seecheran, Naveen Seebalack, Victoria Seecheran, Rajeev Maharaj, Aarti Boodhai, Brent Seecheran, Valmiki Persad, Sangeeta Motilal, Shastri Tello-Montoliu, Antonio Schneider, David Cardiol Ther Original Research INTRODUCTION: This prospective study aimed to determine whether trimetazidine (TMZ) alters the pharmacodynamic (PD) effects of clopidogrel. METHODS: Patients with stable coronary artery disease (SCAD) (n = 24) who were actively treated with dual antiplatelet therapy (DAPT) of aspirin 81 mg daily and clopidogrel 75 mg daily were recruited. Platelet function was measured with the VerifyNow P2Y12 assay (Accriva Diagnostics, San Diego, CA, USA) and assessed before the initiation of and after 14 days of treatment with TMZ. Results were compared using a paired t test. RESULTS: Almost 80% of the study population were of South Asian descent and had diabetes mellitus (DM). P2Y12 reaction units (PRUs) were higher in patients on TMZ (204 ± 56 compared with 174 ± 71 before TMZ, p = 0.005). The average increase in PRU score was 29 (95% confidence interval 8.8–49.7). Before TMZ, the proportion of patients with high on-treatment platelet reactivity (PRU > 208 units) was 25%, which increased to 42% for patients on TMZ. CONCLUSION: Higher platelet reactivity was seen in patients on TMZ, suggesting that TMZ attenuated the PD effects of clopidogrel in this study of a predominantly South Asian diabetic subpopulation. Alternative therapies should be considered and further research is warranted. TRIAL REGISTRATION: ClinicalTrials.gov number, NCT03603249. Springer Healthcare 2019-07-10 2019-12 /pmc/articles/PMC6828882/ /pubmed/31292901 http://dx.doi.org/10.1007/s40119-019-0139-0 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Seecheran, Naveen
Seebalack, Victoria
Seecheran, Rajeev
Maharaj, Aarti
Boodhai, Brent
Seecheran, Valmiki
Persad, Sangeeta
Motilal, Shastri
Tello-Montoliu, Antonio
Schneider, David
TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title_full TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title_fullStr TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title_full_unstemmed TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title_short TRimetazidine as an Agent to affeCt clopidogrEl Response: The TRACER Study
title_sort trimetazidine as an agent to affect clopidogrel response: the tracer study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828882/
https://www.ncbi.nlm.nih.gov/pubmed/31292901
http://dx.doi.org/10.1007/s40119-019-0139-0
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