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Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease

BACKGROUND: Expression and activity of the fibroblast growth factor (FGF) 21 hormone-like protein are associated with development of several metabolic disorders. This study was designed to investigate whether serum FGF21 level was also associated with the metabolic syndrome-related cardiovascular di...

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Autores principales: Shen, Yun, Ma, Xiaojing, Zhou, Jian, Pan, Xiaoping, Hao, Yaping, Zhou, Mi, Lu, Zhigang, Gao, Meifang, 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/PMC3766150/
https://www.ncbi.nlm.nih.gov/pubmed/23981342
http://dx.doi.org/10.1186/1475-2840-12-124
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author Shen, Yun
Ma, Xiaojing
Zhou, Jian
Pan, Xiaoping
Hao, Yaping
Zhou, Mi
Lu, Zhigang
Gao, Meifang
Bao, Yuqian
Jia, Weiping
author_facet Shen, Yun
Ma, Xiaojing
Zhou, Jian
Pan, Xiaoping
Hao, Yaping
Zhou, Mi
Lu, Zhigang
Gao, Meifang
Bao, Yuqian
Jia, Weiping
author_sort Shen, Yun
collection PubMed
description BACKGROUND: Expression and activity of the fibroblast growth factor (FGF) 21 hormone-like protein are associated with development of several metabolic disorders. This study was designed to investigate whether serum FGF21 level was also associated with the metabolic syndrome-related cardiovascular disease, atherosclerosis, and its clinical features in a Chinese cohort. METHODS: Two-hundred-and-fifty-three subjects visiting the Cardiology Department (Sixth People's Hospital affiliated to Shanghai JiaoTong University) were examined by coronary arteriography (to diagnose coronary artery disease (CAD)) and hepatic ultrasonography (to diagnose non-alcoholic fatty liver disease (NAFLD)). Serum FGF21 level was measured by enzyme-linked immunosorbent assay and analyzed for correlation to subject and clinical characteristics. The independent factors of CAD were determined by multivariate logistic regression analysis. RESULTS: Subjects with NAFLD showed significantly higher serum FGF21 than those without NAFLD (388.0 pg/mL (253.0-655.4) vs. 273.3 pg/mL (164.9-383.7), P < 0.01). Subjects with CAD showed significantly higher serum FGF21, regardless of NAFLD diagnosis (P < 0.05). Serum FGF21 level significantly elevated with the increasing number of metabolic disorders (P for trend < 0.01). After adjustment of age, sex, and BMI, FGF21 was positively correlated with total cholesterol (P < 0.05) and triglyceride (P < 0.01). FGF21 was identified as an independent factor of CAD (odds ratio = 2.984, 95% confidence interval: 1.014-8.786, P < 0.05). CONCLUSIONS: Increased level of serum FGF21 is associated with NAFLD, metabolic disorders and CAD.
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spelling pubmed-37661502013-09-08 Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease Shen, Yun Ma, Xiaojing Zhou, Jian Pan, Xiaoping Hao, Yaping Zhou, Mi Lu, Zhigang Gao, Meifang Bao, Yuqian Jia, Weiping Cardiovasc Diabetol Original Investigation BACKGROUND: Expression and activity of the fibroblast growth factor (FGF) 21 hormone-like protein are associated with development of several metabolic disorders. This study was designed to investigate whether serum FGF21 level was also associated with the metabolic syndrome-related cardiovascular disease, atherosclerosis, and its clinical features in a Chinese cohort. METHODS: Two-hundred-and-fifty-three subjects visiting the Cardiology Department (Sixth People's Hospital affiliated to Shanghai JiaoTong University) were examined by coronary arteriography (to diagnose coronary artery disease (CAD)) and hepatic ultrasonography (to diagnose non-alcoholic fatty liver disease (NAFLD)). Serum FGF21 level was measured by enzyme-linked immunosorbent assay and analyzed for correlation to subject and clinical characteristics. The independent factors of CAD were determined by multivariate logistic regression analysis. RESULTS: Subjects with NAFLD showed significantly higher serum FGF21 than those without NAFLD (388.0 pg/mL (253.0-655.4) vs. 273.3 pg/mL (164.9-383.7), P < 0.01). Subjects with CAD showed significantly higher serum FGF21, regardless of NAFLD diagnosis (P < 0.05). Serum FGF21 level significantly elevated with the increasing number of metabolic disorders (P for trend < 0.01). After adjustment of age, sex, and BMI, FGF21 was positively correlated with total cholesterol (P < 0.05) and triglyceride (P < 0.01). FGF21 was identified as an independent factor of CAD (odds ratio = 2.984, 95% confidence interval: 1.014-8.786, P < 0.05). CONCLUSIONS: Increased level of serum FGF21 is associated with NAFLD, metabolic disorders and CAD. BioMed Central 2013-08-28 /pmc/articles/PMC3766150/ /pubmed/23981342 http://dx.doi.org/10.1186/1475-2840-12-124 Text en Copyright © 2013 Shen 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
Shen, Yun
Ma, Xiaojing
Zhou, Jian
Pan, Xiaoping
Hao, Yaping
Zhou, Mi
Lu, Zhigang
Gao, Meifang
Bao, Yuqian
Jia, Weiping
Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title_full Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title_fullStr Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title_full_unstemmed Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title_short Additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
title_sort additive relationship between serum fibroblast growth factor 21 level and coronary artery disease
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766150/
https://www.ncbi.nlm.nih.gov/pubmed/23981342
http://dx.doi.org/10.1186/1475-2840-12-124
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