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Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease
OBJECTIVE: Antioxidants play a major role in the cellular protection cascade against oxidative damage. Oxidative stress has been linked to the pathogenesis of coronary atherosclerosis. Our aim was to evaluate the association between calculated serum total antioxidant status (cTAS) and the presence a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331354/ https://www.ncbi.nlm.nih.gov/pubmed/27488746 http://dx.doi.org/10.5152/AnatolJCardiol.2015.6482 |
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author | Anvari, Maryam Sotoudeh Babaki, Maryam Mortazavian Boroumand, Mohammad Ali Eslami, Bahareh Jalali, Arash Goodarzynejad, Hamidreza |
author_facet | Anvari, Maryam Sotoudeh Babaki, Maryam Mortazavian Boroumand, Mohammad Ali Eslami, Bahareh Jalali, Arash Goodarzynejad, Hamidreza |
author_sort | Anvari, Maryam Sotoudeh |
collection | PubMed |
description | OBJECTIVE: Antioxidants play a major role in the cellular protection cascade against oxidative damage. Oxidative stress has been linked to the pathogenesis of coronary atherosclerosis. Our aim was to evaluate the association between calculated serum total antioxidant status (cTAS) and the presence and severity of coronary artery disease (CAD). METHODS: One hundred and seventy-four patients with angiographically documented significant (≥50%) luminal stenosis (n=123) or with minimal (<50%) luminal stenosis (n=51) in at least one coronary artery or major branch segment in the epicardial coronary tree were categorized as CAD(+) group; 88 patients with no luminal stenosis were considered as the control group. The level of cTAS (mmol/L) was evaluated using the following equation: (0.63´albumin concentration)+(1.02´uric acid concentration)+(1.53´bilirubin concentration). RESULTS: In univariate analyses, mean levels of cTAS, uric acid, and creatinine were significantly higher in CAD(+) group than in controls. However, adjusted cTAS level was not found to be a CAD predictor in the total population [odds ratio (OR)=1.20; 95% confidence interval (CI): 0.81–1.76; p=0.364] or in men (OR=1.25; 95% CI: 0.73–2.12; p=0.420) and women (OR=1.20; 95% CI: 0.66–2.19; p=0.553). A weak but statistically significant correlation was found between cTAS and Gensini score (Spearman’s r=0.16, p=0.015). CONCLUSION: In patients with suspicious CAD, the level of cTAS was not found to be an independent predictor for the presence of CAD. Further studies with larger sample size are required to confirm the results. |
format | Online Article Text |
id | pubmed-5331354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53313542017-06-28 Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease Anvari, Maryam Sotoudeh Babaki, Maryam Mortazavian Boroumand, Mohammad Ali Eslami, Bahareh Jalali, Arash Goodarzynejad, Hamidreza Anatol J Cardiol Original Investigation OBJECTIVE: Antioxidants play a major role in the cellular protection cascade against oxidative damage. Oxidative stress has been linked to the pathogenesis of coronary atherosclerosis. Our aim was to evaluate the association between calculated serum total antioxidant status (cTAS) and the presence and severity of coronary artery disease (CAD). METHODS: One hundred and seventy-four patients with angiographically documented significant (≥50%) luminal stenosis (n=123) or with minimal (<50%) luminal stenosis (n=51) in at least one coronary artery or major branch segment in the epicardial coronary tree were categorized as CAD(+) group; 88 patients with no luminal stenosis were considered as the control group. The level of cTAS (mmol/L) was evaluated using the following equation: (0.63´albumin concentration)+(1.02´uric acid concentration)+(1.53´bilirubin concentration). RESULTS: In univariate analyses, mean levels of cTAS, uric acid, and creatinine were significantly higher in CAD(+) group than in controls. However, adjusted cTAS level was not found to be a CAD predictor in the total population [odds ratio (OR)=1.20; 95% confidence interval (CI): 0.81–1.76; p=0.364] or in men (OR=1.25; 95% CI: 0.73–2.12; p=0.420) and women (OR=1.20; 95% CI: 0.66–2.19; p=0.553). A weak but statistically significant correlation was found between cTAS and Gensini score (Spearman’s r=0.16, p=0.015). CONCLUSION: In patients with suspicious CAD, the level of cTAS was not found to be an independent predictor for the presence of CAD. Further studies with larger sample size are required to confirm the results. Kare Publishing 2016-09 2015-11-26 /pmc/articles/PMC5331354/ /pubmed/27488746 http://dx.doi.org/10.5152/AnatolJCardiol.2015.6482 Text en Copyright © 2016 Turkish Society of Cardiology 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 Investigation Anvari, Maryam Sotoudeh Babaki, Maryam Mortazavian Boroumand, Mohammad Ali Eslami, Bahareh Jalali, Arash Goodarzynejad, Hamidreza Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title | Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title_full | Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title_fullStr | Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title_full_unstemmed | Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title_short | Relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
title_sort | relationship between calculated total antioxidant status and atherosclerotic coronary artery disease |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331354/ https://www.ncbi.nlm.nih.gov/pubmed/27488746 http://dx.doi.org/10.5152/AnatolJCardiol.2015.6482 |
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