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The association between aspirin resistance and extent and severity of coronary atherosclerosis

OBJECTIVE: Uncontrolled inflammatory responses could contribute to the pathogenesis of many leading causes of human morbidity and mortality. Aspirin is an anti-inflammatory and antithrombotic drug that is used in the primary and secondary protection in atherothrombotic diseases and complications. Th...

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Autores principales: Kahraman, Serkan, Dogan, Ali, Ziyrek, Murat, Usta, Emrah, Demiroz, Onder, Ciftci, Cavlan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371993/
https://www.ncbi.nlm.nih.gov/pubmed/30859163
http://dx.doi.org/10.14744/nci.2017.26779
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author Kahraman, Serkan
Dogan, Ali
Ziyrek, Murat
Usta, Emrah
Demiroz, Onder
Ciftci, Cavlan
author_facet Kahraman, Serkan
Dogan, Ali
Ziyrek, Murat
Usta, Emrah
Demiroz, Onder
Ciftci, Cavlan
author_sort Kahraman, Serkan
collection PubMed
description OBJECTIVE: Uncontrolled inflammatory responses could contribute to the pathogenesis of many leading causes of human morbidity and mortality. Aspirin is an anti-inflammatory and antithrombotic drug that is used in the primary and secondary protection in atherothrombotic diseases and complications. The aim of the present study was to analyze the effect of aspirin resistance on the extent and severity of atherosclerosis. METHODS: One hundred patients who underwent coronary angiography with suspected or known coronary artery disease and were using aspirin were enrolled in the study. RESULTS: Of these 100 patients, 30 (8 female and 22 male) formed the aspirin-resistant group (ARG), and 70 (22 female and 48 male) formed the control group. Gensini scoring system (GSS) was significantly higher in the ARG than in the control group (80.5 (36–166) vs. 45 (2–209); p<0.001). The number of percutaneous coronary intervention (PCI) patients was significantly higher in the ARG (13 of 30 (43.3%) ARG vs. 13 of 70 (18.6%) control group; p=0.01). Furthermore, when we evaluate the 16 reintervention patients, stent restenosis was significantly higher in the ARG (11 of 16 (68.75%) ARG vs. 5 of 16 (31.25%) control group; p=0.016). Multivariate logistic regression analysis revealed that GSS (p=0.038; 95% CI: 1.001–1.026) and PCI history (p=0.017; 95% CI: 1.182–89.804) were independent risk factors for aspirin resistance. CONCLUSION: In conclusion, atherosclerotic burden as calculated by the GSS is significantly higher in aspirin-resistant patients. According to this result, we suggest that aspirin treatment can be prescribed in higher doses in aspirin resistance patients with coronary events. Furthermore, GSS and PCI history could be independent predictors of aspirin resistance.
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spelling pubmed-63719932019-03-11 The association between aspirin resistance and extent and severity of coronary atherosclerosis Kahraman, Serkan Dogan, Ali Ziyrek, Murat Usta, Emrah Demiroz, Onder Ciftci, Cavlan North Clin Istanb Original Article OBJECTIVE: Uncontrolled inflammatory responses could contribute to the pathogenesis of many leading causes of human morbidity and mortality. Aspirin is an anti-inflammatory and antithrombotic drug that is used in the primary and secondary protection in atherothrombotic diseases and complications. The aim of the present study was to analyze the effect of aspirin resistance on the extent and severity of atherosclerosis. METHODS: One hundred patients who underwent coronary angiography with suspected or known coronary artery disease and were using aspirin were enrolled in the study. RESULTS: Of these 100 patients, 30 (8 female and 22 male) formed the aspirin-resistant group (ARG), and 70 (22 female and 48 male) formed the control group. Gensini scoring system (GSS) was significantly higher in the ARG than in the control group (80.5 (36–166) vs. 45 (2–209); p<0.001). The number of percutaneous coronary intervention (PCI) patients was significantly higher in the ARG (13 of 30 (43.3%) ARG vs. 13 of 70 (18.6%) control group; p=0.01). Furthermore, when we evaluate the 16 reintervention patients, stent restenosis was significantly higher in the ARG (11 of 16 (68.75%) ARG vs. 5 of 16 (31.25%) control group; p=0.016). Multivariate logistic regression analysis revealed that GSS (p=0.038; 95% CI: 1.001–1.026) and PCI history (p=0.017; 95% CI: 1.182–89.804) were independent risk factors for aspirin resistance. CONCLUSION: In conclusion, atherosclerotic burden as calculated by the GSS is significantly higher in aspirin-resistant patients. According to this result, we suggest that aspirin treatment can be prescribed in higher doses in aspirin resistance patients with coronary events. Furthermore, GSS and PCI history could be independent predictors of aspirin resistance. Kare Publishing 2018-08-08 /pmc/articles/PMC6371993/ /pubmed/30859163 http://dx.doi.org/10.14744/nci.2017.26779 Text en Copyright: © 2018 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Original Article
Kahraman, Serkan
Dogan, Ali
Ziyrek, Murat
Usta, Emrah
Demiroz, Onder
Ciftci, Cavlan
The association between aspirin resistance and extent and severity of coronary atherosclerosis
title The association between aspirin resistance and extent and severity of coronary atherosclerosis
title_full The association between aspirin resistance and extent and severity of coronary atherosclerosis
title_fullStr The association between aspirin resistance and extent and severity of coronary atherosclerosis
title_full_unstemmed The association between aspirin resistance and extent and severity of coronary atherosclerosis
title_short The association between aspirin resistance and extent and severity of coronary atherosclerosis
title_sort association between aspirin resistance and extent and severity of coronary atherosclerosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371993/
https://www.ncbi.nlm.nih.gov/pubmed/30859163
http://dx.doi.org/10.14744/nci.2017.26779
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