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Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors

Background: Previous studies have shown that Asymmetric Dimethyl Arginine (ADMA) is increased significantly during coronary artery diseases (CAD). However it is not clear either this increase is due to cardiovascular disease (CVD) risk factors or ADMA is increased independently in CAD. The aim of th...

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Autores principales: Ghayour-Mobarhan, Majid, Ayati, Nayyereh, Sahebkar, Amir Hossein, Moohebati, Mohsen, Ayati, Narjess, Elyasi, Sepideh, Mohammadpour, Amir Hooshang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179032/
https://www.ncbi.nlm.nih.gov/pubmed/29957752
http://dx.doi.org/10.23750/abm.v89i2.5335
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author Ghayour-Mobarhan, Majid
Ayati, Nayyereh
Sahebkar, Amir Hossein
Moohebati, Mohsen
Ayati, Narjess
Elyasi, Sepideh
Mohammadpour, Amir Hooshang
author_facet Ghayour-Mobarhan, Majid
Ayati, Nayyereh
Sahebkar, Amir Hossein
Moohebati, Mohsen
Ayati, Narjess
Elyasi, Sepideh
Mohammadpour, Amir Hooshang
author_sort Ghayour-Mobarhan, Majid
collection PubMed
description Background: Previous studies have shown that Asymmetric Dimethyl Arginine (ADMA) is increased significantly during coronary artery diseases (CAD). However it is not clear either this increase is due to cardiovascular disease (CVD) risk factors or ADMA is increased independently in CAD. The aim of this study is to evaluate ADMA’s plasma level as an independent biomarker in CADs. Patients and methods: In current study a total of 165 subjects with no traditional CVD’s RFs, who fulfilled the inclusion and exclusion criteria, were recruited; 55 CAD+ patients which had more than 50% stenosis (CAD+); 55 CAD- patients which had less than 50% stenosis in their coronary arteries (CAD-), based on their angiography record and 55 healthy individuals as controls. CAD+ patients were divided into three groups: single (SVD), double (2VD), and triple vessel (3VD) disease. Plasma level of soluble ADMA was measured with an enzyme-linked immono sorbent assay (ELISA) kit. Results: No significant difference between ADMA’s plasma levels was found between CAD+, CAD- and healthy groups. In addition ADMA’s plasma levels was not significantly different between CAD+’s subgroups. Conclusions: The result of this study indicates no significant relation between ADMA’s plasma levels and either presence or severity of coronary artery stenosis. Therefore, it is presumed that ADMA may not be an independent biomarker for CADs. (www.actabiomedica.it)
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spelling pubmed-61790322019-05-08 Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors Ghayour-Mobarhan, Majid Ayati, Nayyereh Sahebkar, Amir Hossein Moohebati, Mohsen Ayati, Narjess Elyasi, Sepideh Mohammadpour, Amir Hooshang Acta Biomed Original Article Background: Previous studies have shown that Asymmetric Dimethyl Arginine (ADMA) is increased significantly during coronary artery diseases (CAD). However it is not clear either this increase is due to cardiovascular disease (CVD) risk factors or ADMA is increased independently in CAD. The aim of this study is to evaluate ADMA’s plasma level as an independent biomarker in CADs. Patients and methods: In current study a total of 165 subjects with no traditional CVD’s RFs, who fulfilled the inclusion and exclusion criteria, were recruited; 55 CAD+ patients which had more than 50% stenosis (CAD+); 55 CAD- patients which had less than 50% stenosis in their coronary arteries (CAD-), based on their angiography record and 55 healthy individuals as controls. CAD+ patients were divided into three groups: single (SVD), double (2VD), and triple vessel (3VD) disease. Plasma level of soluble ADMA was measured with an enzyme-linked immono sorbent assay (ELISA) kit. Results: No significant difference between ADMA’s plasma levels was found between CAD+, CAD- and healthy groups. In addition ADMA’s plasma levels was not significantly different between CAD+’s subgroups. Conclusions: The result of this study indicates no significant relation between ADMA’s plasma levels and either presence or severity of coronary artery stenosis. Therefore, it is presumed that ADMA may not be an independent biomarker for CADs. (www.actabiomedica.it) Mattioli 1885 2018 /pmc/articles/PMC6179032/ /pubmed/29957752 http://dx.doi.org/10.23750/abm.v89i2.5335 Text en Copyright: © 2018 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article
Ghayour-Mobarhan, Majid
Ayati, Nayyereh
Sahebkar, Amir Hossein
Moohebati, Mohsen
Ayati, Narjess
Elyasi, Sepideh
Mohammadpour, Amir Hooshang
Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title_full Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title_fullStr Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title_full_unstemmed Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title_short Evaluation of serum Asymmetric Dimethyl Arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
title_sort evaluation of serum asymmetric dimethyl arginine concentrations in coronary artery disease patients without traditional cardiovascular risk factors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6179032/
https://www.ncbi.nlm.nih.gov/pubmed/29957752
http://dx.doi.org/10.23750/abm.v89i2.5335
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