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Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease
Objective : Several studies have demonstrated the beneficial role of antiplatelet therapy with acetylsalicylic acid (ASA) at atherosclerotic vascular disease. Antiaggregant effect of ASA is not uniform in all patients. Purpose of the present study is to evaluate the prevalence of ASA resistance in p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Professional Medical Publicaitons
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048502/ https://www.ncbi.nlm.nih.gov/pubmed/24948975 http://dx.doi.org/10.12669/pjms.303.4773 |
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author | Cetin, Mustafa Kiziltunc, Emrullah Cetin, Zehra Guven Cicekcioglu, Hulya Sahin, Muslum Isik, Serhat Kurtul, Alparslan Ornek, Ender Ulusoy, Feridun Vasfi |
author_facet | Cetin, Mustafa Kiziltunc, Emrullah Cetin, Zehra Guven Cicekcioglu, Hulya Sahin, Muslum Isik, Serhat Kurtul, Alparslan Ornek, Ender Ulusoy, Feridun Vasfi |
author_sort | Cetin, Mustafa |
collection | PubMed |
description | Objective : Several studies have demonstrated the beneficial role of antiplatelet therapy with acetylsalicylic acid (ASA) at atherosclerotic vascular disease. Antiaggregant effect of ASA is not uniform in all patients. Purpose of the present study is to evaluate the prevalence of ASA resistance in patients with type 2 diabetes mellitus (T2DM), pre-diabetes and non-diabetic coronary artery disease (CAD). Methods: Effect of ASA was assessed using the platelet function analyzer (PFA-100) system. Resistance to ASA was defined as a normal collagen/epinephrine induced closure time after one week of ASA therapy. Patients with non-diabetic CAD, pre-diabetes and T2DM were compared. Results: ASA resistance was found in 26 (37.1%), 6 (17.6%) and 41 (26.5%) patients in the groups, respectively (p=0.154). ASA resistance was found to be significantly higher in men, smokers and insulin users, besides this it was found to be significantly lower in beta blocker (BB) users, angiotensin converting enzyme inhibitor (ACEI) users with univariate analysis. However insulin usage was found to be the single effective parameter on ASA resistance in multivariate analysis. Conclusion: There was no difference with regard to ASA resistance between groups. While ASA resistance was higher in men, smokers and insulin users, it was lower in patients using BBs and ACEIs. |
format | Online Article Text |
id | pubmed-4048502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Professional Medical Publicaitons |
record_format | MEDLINE/PubMed |
spelling | pubmed-40485022014-06-19 Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease Cetin, Mustafa Kiziltunc, Emrullah Cetin, Zehra Guven Cicekcioglu, Hulya Sahin, Muslum Isik, Serhat Kurtul, Alparslan Ornek, Ender Ulusoy, Feridun Vasfi Pak J Med Sci Original Article Objective : Several studies have demonstrated the beneficial role of antiplatelet therapy with acetylsalicylic acid (ASA) at atherosclerotic vascular disease. Antiaggregant effect of ASA is not uniform in all patients. Purpose of the present study is to evaluate the prevalence of ASA resistance in patients with type 2 diabetes mellitus (T2DM), pre-diabetes and non-diabetic coronary artery disease (CAD). Methods: Effect of ASA was assessed using the platelet function analyzer (PFA-100) system. Resistance to ASA was defined as a normal collagen/epinephrine induced closure time after one week of ASA therapy. Patients with non-diabetic CAD, pre-diabetes and T2DM were compared. Results: ASA resistance was found in 26 (37.1%), 6 (17.6%) and 41 (26.5%) patients in the groups, respectively (p=0.154). ASA resistance was found to be significantly higher in men, smokers and insulin users, besides this it was found to be significantly lower in beta blocker (BB) users, angiotensin converting enzyme inhibitor (ACEI) users with univariate analysis. However insulin usage was found to be the single effective parameter on ASA resistance in multivariate analysis. Conclusion: There was no difference with regard to ASA resistance between groups. While ASA resistance was higher in men, smokers and insulin users, it was lower in patients using BBs and ACEIs. Professional Medical Publicaitons 2014 /pmc/articles/PMC4048502/ /pubmed/24948975 http://dx.doi.org/10.12669/pjms.303.4773 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Cetin, Mustafa Kiziltunc, Emrullah Cetin, Zehra Guven Cicekcioglu, Hulya Sahin, Muslum Isik, Serhat Kurtul, Alparslan Ornek, Ender Ulusoy, Feridun Vasfi Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title | Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title_full | Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title_fullStr | Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title_full_unstemmed | Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title_short | Acetylsalicylic Acid Resistance in Patients with Type 2 Diabetes Mellitus, Prediabetes & Non-Diabetic Coronary Artery Disease |
title_sort | acetylsalicylic acid resistance in patients with type 2 diabetes mellitus, prediabetes & non-diabetic coronary artery disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048502/ https://www.ncbi.nlm.nih.gov/pubmed/24948975 http://dx.doi.org/10.12669/pjms.303.4773 |
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