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Clinical implications of plasma Nogo-A levels in patients with coronary heart disease

INTRODUCTION: Nogo-A is an important neurite growth-regulatory protein in the adult and developing nervous system. Recently, increasing evidence has shown that Nogo-A plays important roles in cardiac development and may act as a potential indicator for heart failure. In addition, increased oxidative...

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Autores principales: Ding, Yu, Gao, Bei-Bei, Zhou, Liang, Ye, Xian-Hua, Li, Hong, Lai, Lei, Huang, Jin-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510510/
https://www.ncbi.nlm.nih.gov/pubmed/28721144
http://dx.doi.org/10.5114/aoms.2016.58713
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author Ding, Yu
Gao, Bei-Bei
Zhou, Liang
Ye, Xian-Hua
Li, Hong
Lai, Lei
Huang, Jin-Yu
author_facet Ding, Yu
Gao, Bei-Bei
Zhou, Liang
Ye, Xian-Hua
Li, Hong
Lai, Lei
Huang, Jin-Yu
author_sort Ding, Yu
collection PubMed
description INTRODUCTION: Nogo-A is an important neurite growth-regulatory protein in the adult and developing nervous system. Recently, increasing evidence has shown that Nogo-A plays important roles in cardiac development and may act as a potential indicator for heart failure. In addition, increased oxidative stress has been found in individuals with cardiovascular diseases. However, not much is known regarding the expression levels of Nogo-A and reactive oxygen species (ROS) in patients with coronary heart disease (CHD). Therefore, we sought to investigate the relationship between Nogo-A, ROS levels and CHD. MATERIAL AND METHODS: The plasma Nogo-A and ROS concentrations of 122 acute coronary syndrome (ACS), 101 unstable angina pectoris (UAP), and 21 acute myocardial infarction (AMI) patients and 56 healthy controls were measured by enzyme-linked immunosorbent assay (ELISA). We further generated a receiver operating characteristic (ROC) curve to assess the diagnostic accuracy of Nogo-A and ROS in CHD. RESULTS: The Nogo-A and ROS levels were significantly higher in patients with CHD than those in healthy controls. In addition, multivariate logistic regression analysis revealed that the level of Nogo-A (odds ratio (OR) = 1.624, 95% confidence interval: 1.125–2.293, p = 0.009) is a risk factor for prediction of CHD. Nogo-A has diagnostic value, with an optimal threshold of 5.466 ng/ml for maximized diagnostic performance (59% sensitivity and 78.6% specificity, area under curve, p < 0.05). However, ROS concentration is not a risk factor for prediction of CHD (OR = 0.999, 95% confidence interval: 0.997–1.001, p = 0.320). CONCLUSIONS: Increased plasma Nogo-A level may be associated with CHD.
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spelling pubmed-55105102017-07-18 Clinical implications of plasma Nogo-A levels in patients with coronary heart disease Ding, Yu Gao, Bei-Bei Zhou, Liang Ye, Xian-Hua Li, Hong Lai, Lei Huang, Jin-Yu Arch Med Sci Clinical Research INTRODUCTION: Nogo-A is an important neurite growth-regulatory protein in the adult and developing nervous system. Recently, increasing evidence has shown that Nogo-A plays important roles in cardiac development and may act as a potential indicator for heart failure. In addition, increased oxidative stress has been found in individuals with cardiovascular diseases. However, not much is known regarding the expression levels of Nogo-A and reactive oxygen species (ROS) in patients with coronary heart disease (CHD). Therefore, we sought to investigate the relationship between Nogo-A, ROS levels and CHD. MATERIAL AND METHODS: The plasma Nogo-A and ROS concentrations of 122 acute coronary syndrome (ACS), 101 unstable angina pectoris (UAP), and 21 acute myocardial infarction (AMI) patients and 56 healthy controls were measured by enzyme-linked immunosorbent assay (ELISA). We further generated a receiver operating characteristic (ROC) curve to assess the diagnostic accuracy of Nogo-A and ROS in CHD. RESULTS: The Nogo-A and ROS levels were significantly higher in patients with CHD than those in healthy controls. In addition, multivariate logistic regression analysis revealed that the level of Nogo-A (odds ratio (OR) = 1.624, 95% confidence interval: 1.125–2.293, p = 0.009) is a risk factor for prediction of CHD. Nogo-A has diagnostic value, with an optimal threshold of 5.466 ng/ml for maximized diagnostic performance (59% sensitivity and 78.6% specificity, area under curve, p < 0.05). However, ROS concentration is not a risk factor for prediction of CHD (OR = 0.999, 95% confidence interval: 0.997–1.001, p = 0.320). CONCLUSIONS: Increased plasma Nogo-A level may be associated with CHD. Termedia Publishing House 2016-03-23 2017-06 /pmc/articles/PMC5510510/ /pubmed/28721144 http://dx.doi.org/10.5114/aoms.2016.58713 Text en Copyright: © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Ding, Yu
Gao, Bei-Bei
Zhou, Liang
Ye, Xian-Hua
Li, Hong
Lai, Lei
Huang, Jin-Yu
Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title_full Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title_fullStr Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title_full_unstemmed Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title_short Clinical implications of plasma Nogo-A levels in patients with coronary heart disease
title_sort clinical implications of plasma nogo-a levels in patients with coronary heart disease
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510510/
https://www.ncbi.nlm.nih.gov/pubmed/28721144
http://dx.doi.org/10.5114/aoms.2016.58713
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