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High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome

BACKGROUND: Metabolic syndrome is known to be a prothrombotic state. We undertook this study to examine a hypothesis that aspirin resistance may be associated with metabolic syndrome, and to assess other potential determinants of aspirin resistance in patients with cardiovascular disease (CVD). METH...

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Autores principales: Liu, Lin, Gao, Ying-Hui, Cao, Jian, Zhang, Hua-Xin, Fan, Li, Hu, Guo-Liang, Hu, Yi-Xin, Li, Xiao-Li, Zou, Xiao, Li, Jian-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987425/
https://www.ncbi.nlm.nih.gov/pubmed/27582771
http://dx.doi.org/10.11909/j.issn.1671-5411.2016.06.009
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author Liu, Lin
Gao, Ying-Hui
Cao, Jian
Zhang, Hua-Xin
Fan, Li
Hu, Guo-Liang
Hu, Yi-Xin
Li, Xiao-Li
Zou, Xiao
Li, Jian-Hua
author_facet Liu, Lin
Gao, Ying-Hui
Cao, Jian
Zhang, Hua-Xin
Fan, Li
Hu, Guo-Liang
Hu, Yi-Xin
Li, Xiao-Li
Zou, Xiao
Li, Jian-Hua
author_sort Liu, Lin
collection PubMed
description BACKGROUND: Metabolic syndrome is known to be a prothrombotic state. We undertook this study to examine a hypothesis that aspirin resistance may be associated with metabolic syndrome, and to assess other potential determinants of aspirin resistance in patients with cardiovascular disease (CVD). METHODS: A total of 469 elderly patients with CVD were recruited. One hundred and seventy-two patients with metabolic syndrome and 297 without metabolic syndrome (control group) received daily aspirin therapy (≥ 75 mg) over one month. Platelet aggregation was measured by light transmission aggregometry (LTA). Aspirin resistance was defined as ≥ 20% arachidonic acid (AA)- and ≥ 70% adenosine diphosphate (ADP)-induced aggregation according to LTA. Aspirin semi-responders were defined as meeting one (but not both) of these criteria. RESULTS: By LTA, 38 of 469 (8.1%) patients were aspirin resistant. The prevalence of aspirin resistance was higher in the metabolic syndrome group compared with the control group [11.6 % vs. 6.6%, odds ratio (OR) = 2.039; 95% confidence interval (CI): 1.047–3.973]. In the multivariate logistic regression analysis, metabolic syndrome (OR = 4.951, 95% CI: 1.440–17.019, P = 0.011) was a significant risk factor for aspirin resistance. CONCLUSIONS: A significant number of patients with CVD and metabolic syndrome are resistant to aspirin therapy. This might further increase the risk of cardiovascular morbidity and mortality in these patients.
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spelling pubmed-49874252016-09-01 High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome Liu, Lin Gao, Ying-Hui Cao, Jian Zhang, Hua-Xin Fan, Li Hu, Guo-Liang Hu, Yi-Xin Li, Xiao-Li Zou, Xiao Li, Jian-Hua J Geriatr Cardiol Research Article BACKGROUND: Metabolic syndrome is known to be a prothrombotic state. We undertook this study to examine a hypothesis that aspirin resistance may be associated with metabolic syndrome, and to assess other potential determinants of aspirin resistance in patients with cardiovascular disease (CVD). METHODS: A total of 469 elderly patients with CVD were recruited. One hundred and seventy-two patients with metabolic syndrome and 297 without metabolic syndrome (control group) received daily aspirin therapy (≥ 75 mg) over one month. Platelet aggregation was measured by light transmission aggregometry (LTA). Aspirin resistance was defined as ≥ 20% arachidonic acid (AA)- and ≥ 70% adenosine diphosphate (ADP)-induced aggregation according to LTA. Aspirin semi-responders were defined as meeting one (but not both) of these criteria. RESULTS: By LTA, 38 of 469 (8.1%) patients were aspirin resistant. The prevalence of aspirin resistance was higher in the metabolic syndrome group compared with the control group [11.6 % vs. 6.6%, odds ratio (OR) = 2.039; 95% confidence interval (CI): 1.047–3.973]. In the multivariate logistic regression analysis, metabolic syndrome (OR = 4.951, 95% CI: 1.440–17.019, P = 0.011) was a significant risk factor for aspirin resistance. CONCLUSIONS: A significant number of patients with CVD and metabolic syndrome are resistant to aspirin therapy. This might further increase the risk of cardiovascular morbidity and mortality in these patients. Science Press 2016-09 /pmc/articles/PMC4987425/ /pubmed/27582771 http://dx.doi.org/10.11909/j.issn.1671-5411.2016.06.009 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Research Article
Liu, Lin
Gao, Ying-Hui
Cao, Jian
Zhang, Hua-Xin
Fan, Li
Hu, Guo-Liang
Hu, Yi-Xin
Li, Xiao-Li
Zou, Xiao
Li, Jian-Hua
High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title_full High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title_fullStr High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title_full_unstemmed High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title_short High prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
title_sort high prevalence of aspirin resistance in elderly patients with cardiovascular disease and metabolic syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987425/
https://www.ncbi.nlm.nih.gov/pubmed/27582771
http://dx.doi.org/10.11909/j.issn.1671-5411.2016.06.009
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