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Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide
Chlorthalidone (CTD) may be superior to hydrochlorothiazide (HCTZ) in the reduction of adverse cardiovascular events in hypertensive patients. The mechanism of the potential benefit of CTD could be related to antiplatelet effects. The objective of this study was to determine if CTD or HCTZ have anti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581091/ https://www.ncbi.nlm.nih.gov/pubmed/36067089 http://dx.doi.org/10.1111/jch.14564 |
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author | Bashir, Khalid Burns, Tammy Pirruccello, Samuel J. Aurit, Sarah J. Hilleman, Daniel E. |
author_facet | Bashir, Khalid Burns, Tammy Pirruccello, Samuel J. Aurit, Sarah J. Hilleman, Daniel E. |
author_sort | Bashir, Khalid |
collection | PubMed |
description | Chlorthalidone (CTD) may be superior to hydrochlorothiazide (HCTZ) in the reduction of adverse cardiovascular events in hypertensive patients. The mechanism of the potential benefit of CTD could be related to antiplatelet effects. The objective of this study was to determine if CTD or HCTZ have antiplatelet effects. This study was a prospective, double‐blind, randomized, three‐way crossover comparison evaluating the antiplatelet effects of CTD, HCTZ, and aspirin (ASA) in healthy volunteers. The effects of these treatments on platelet activation and aggregation were assessed using a well‐established method with five standard platelet agonists. Thirty‐four patients completed the three‐way crossover comparing pre‐ and post‐treatment changes in platelet activation and aggregation studies. There were statistically significant antiplatelet effects with ASA but not with CTD or HCTZ. Hypokalemia occurred in 0 (0%), 10 (30%), and 6 (18%) of the ASA, CTD, and HCTZ patients, respectively. The results of our study suggest that the benefits of CTD and HCTZ in reducing adverse cardiovascular events in patients with hypertension is not a result of an antiplatelet effect. In our study, hypokalemia with CTD was more prevalent than that reported in a large outcome trial in patients with hypertension. The clinical relevance of this finding is uncertain. |
format | Online Article Text |
id | pubmed-9581091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95810912022-10-20 Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide Bashir, Khalid Burns, Tammy Pirruccello, Samuel J. Aurit, Sarah J. Hilleman, Daniel E. J Clin Hypertens (Greenwich) Adherence Chlorthalidone (CTD) may be superior to hydrochlorothiazide (HCTZ) in the reduction of adverse cardiovascular events in hypertensive patients. The mechanism of the potential benefit of CTD could be related to antiplatelet effects. The objective of this study was to determine if CTD or HCTZ have antiplatelet effects. This study was a prospective, double‐blind, randomized, three‐way crossover comparison evaluating the antiplatelet effects of CTD, HCTZ, and aspirin (ASA) in healthy volunteers. The effects of these treatments on platelet activation and aggregation were assessed using a well‐established method with five standard platelet agonists. Thirty‐four patients completed the three‐way crossover comparing pre‐ and post‐treatment changes in platelet activation and aggregation studies. There were statistically significant antiplatelet effects with ASA but not with CTD or HCTZ. Hypokalemia occurred in 0 (0%), 10 (30%), and 6 (18%) of the ASA, CTD, and HCTZ patients, respectively. The results of our study suggest that the benefits of CTD and HCTZ in reducing adverse cardiovascular events in patients with hypertension is not a result of an antiplatelet effect. In our study, hypokalemia with CTD was more prevalent than that reported in a large outcome trial in patients with hypertension. The clinical relevance of this finding is uncertain. John Wiley and Sons Inc. 2022-09-06 /pmc/articles/PMC9581091/ /pubmed/36067089 http://dx.doi.org/10.1111/jch.14564 Text en © 2022 The Authors. The Journal of Clinical Hypertension published by Wiley Periodicals LLC. 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 | Adherence Bashir, Khalid Burns, Tammy Pirruccello, Samuel J. Aurit, Sarah J. Hilleman, Daniel E. Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title | Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title_full | Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title_fullStr | Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title_full_unstemmed | Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title_short | Comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
title_sort | comparative antiplatelet effects of chlorthalidone and hydrochlorothiazide |
topic | Adherence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581091/ https://www.ncbi.nlm.nih.gov/pubmed/36067089 http://dx.doi.org/10.1111/jch.14564 |
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