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Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease

BACKGROUND: Pigment epithelium-derived factor (PEDF) has been proved to be closely correlated with metabolic syndrome (MetS) and its components that are all risk factors of cardiovascular disease and may play a protective role against vascular injury and atherosclerosis. The present study was design...

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Autores principales: Wang, Feifei, Ma, Xiaojing, Zhou, Mi, Pan, Xiaoping, Ni, Jie, Gao, Meifang, Lu, Zhigang, Hang, Jingyu, Bao, Yuqian, Jia, Weiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626632/
https://www.ncbi.nlm.nih.gov/pubmed/23547730
http://dx.doi.org/10.1186/1475-2840-12-56
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author Wang, Feifei
Ma, Xiaojing
Zhou, Mi
Pan, Xiaoping
Ni, Jie
Gao, Meifang
Lu, Zhigang
Hang, Jingyu
Bao, Yuqian
Jia, Weiping
author_facet Wang, Feifei
Ma, Xiaojing
Zhou, Mi
Pan, Xiaoping
Ni, Jie
Gao, Meifang
Lu, Zhigang
Hang, Jingyu
Bao, Yuqian
Jia, Weiping
author_sort Wang, Feifei
collection PubMed
description BACKGROUND: Pigment epithelium-derived factor (PEDF) has been proved to be closely correlated with metabolic syndrome (MetS) and its components that are all risk factors of cardiovascular disease and may play a protective role against vascular injury and atherosclerosis. The present study was designed to investigate the relationship between serum PEDF and coronary artery disease (CAD). METHODS: A total of 312 consecutive in-patients (including 228 with CAD and 197 with MetS) who underwent coronary angiography were enrolled. Serum PEDF was measured by sandwich enzyme immunoassay and used to carry out multivariate stepwise regression analysis to assess correlation with patient demographic and clinical parameters. Multiple logistic regression analysis was performed to identify factors independently correlated with CAD. RESULTS: Patients with MetS had significantly higher levels of serum PEDF than non-MetS subjects (11.1(8.2, 14.2) vs. 10.1(7.6, 12.4) μg/mL; P < 0.05). Patients with CAD also had significantly higher serum PEDF than non-CAD subjects (11.0(8.1, 14.2) vs. 10.3(8.1, 12.8) μg/mL; P < 0.05). Triglyceride (TG), C-reactive protein (CRP), estimated glomerular filtration rate (eGFR), and hypoglycemic therapy were independently correlated with serum PEDF levels, and serum PEDF was independently positively correlated with CAD. CONCLUSIONS: Serum PEDF levels are independently positively associated with CAD in a Chinese population. Elevated PEDF may act as a protective response against vascular damage and subsequent CAD.
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spelling pubmed-36266322013-04-16 Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease Wang, Feifei Ma, Xiaojing Zhou, Mi Pan, Xiaoping Ni, Jie Gao, Meifang Lu, Zhigang Hang, Jingyu Bao, Yuqian Jia, Weiping Cardiovasc Diabetol Original Investigation BACKGROUND: Pigment epithelium-derived factor (PEDF) has been proved to be closely correlated with metabolic syndrome (MetS) and its components that are all risk factors of cardiovascular disease and may play a protective role against vascular injury and atherosclerosis. The present study was designed to investigate the relationship between serum PEDF and coronary artery disease (CAD). METHODS: A total of 312 consecutive in-patients (including 228 with CAD and 197 with MetS) who underwent coronary angiography were enrolled. Serum PEDF was measured by sandwich enzyme immunoassay and used to carry out multivariate stepwise regression analysis to assess correlation with patient demographic and clinical parameters. Multiple logistic regression analysis was performed to identify factors independently correlated with CAD. RESULTS: Patients with MetS had significantly higher levels of serum PEDF than non-MetS subjects (11.1(8.2, 14.2) vs. 10.1(7.6, 12.4) μg/mL; P < 0.05). Patients with CAD also had significantly higher serum PEDF than non-CAD subjects (11.0(8.1, 14.2) vs. 10.3(8.1, 12.8) μg/mL; P < 0.05). Triglyceride (TG), C-reactive protein (CRP), estimated glomerular filtration rate (eGFR), and hypoglycemic therapy were independently correlated with serum PEDF levels, and serum PEDF was independently positively correlated with CAD. CONCLUSIONS: Serum PEDF levels are independently positively associated with CAD in a Chinese population. Elevated PEDF may act as a protective response against vascular damage and subsequent CAD. BioMed Central 2013-04-01 /pmc/articles/PMC3626632/ /pubmed/23547730 http://dx.doi.org/10.1186/1475-2840-12-56 Text en Copyright © 2013 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Wang, Feifei
Ma, Xiaojing
Zhou, Mi
Pan, Xiaoping
Ni, Jie
Gao, Meifang
Lu, Zhigang
Hang, Jingyu
Bao, Yuqian
Jia, Weiping
Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title_full Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title_fullStr Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title_full_unstemmed Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title_short Serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
title_sort serum pigment epithelium-derived factor levels are independently correlated with the presence of coronary artery disease
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626632/
https://www.ncbi.nlm.nih.gov/pubmed/23547730
http://dx.doi.org/10.1186/1475-2840-12-56
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