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Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris
There is increasing evidence that serum adipokine levels are associated with higher risks of cardiovascular diseases. As an important adipokine, fibroblast growth factor 21 (FGF21) has been demonstrated to be associated with atherosclerosis and coronary artery disease (CAD). However, circulating lev...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153373/ https://www.ncbi.nlm.nih.gov/pubmed/30185439 http://dx.doi.org/10.1042/BSR20181099 |
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author | Cheng, Jing Su, Xing Qiao, Lei Zhai, Chungang Chen, Wenqiang |
author_facet | Cheng, Jing Su, Xing Qiao, Lei Zhai, Chungang Chen, Wenqiang |
author_sort | Cheng, Jing |
collection | PubMed |
description | There is increasing evidence that serum adipokine levels are associated with higher risks of cardiovascular diseases. As an important adipokine, fibroblast growth factor 21 (FGF21) has been demonstrated to be associated with atherosclerosis and coronary artery disease (CAD). However, circulating level of FGF21 in patients with angina pectoris has not yet been investigated. Circulating FGF21 level was examined in 197 patients with stable angina pectoris (SAP, n=66), unstable angina pectoris (UAP, n=76), and control subjects (n=55) along with clinical variables of cardiovascular risk factors. Serum FGF21 concentrations on admission were significantly increased more in patients with UAP than those with SAP (Ln-FGF21: 5.26 ± 0.87 compared with 4.85 ± 0.77, P<0.05) and control subjects (natural logarithm (Ln)-FGF21: 5.26 ± 0.87 compared with 4.54 ± 0.72, P<0.01). The correlation analysis revealed that serum FGF21 concentration was positively correlated with the levels of cardiac troponin I (cTnI) (r(2) = 0.026, P=0.027) and creatine kinase-MB (CK-MB) (r(2) = 0.023, P= 0.04). Furthermore, FGF21 level was identified as an independent factor associated with the risks of UAP (odds ratio (OR): 2.781; 95% CI: 1.476–5.239; P=0.002), after adjusting for gender, age, and body mass index (BMI). However, there were no correlations between serum FGF21 levels and the presence of SAP (OR: 1.248; 95% CI: 0.703–2.215; P=0.448). The present study indicates that FGF21 has a strong correlation and precise predictability for increased risks of UAP, that is independent of traditional risk factors of angina pectoris. |
format | Online Article Text |
id | pubmed-6153373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61533732018-09-25 Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris Cheng, Jing Su, Xing Qiao, Lei Zhai, Chungang Chen, Wenqiang Biosci Rep Research Articles There is increasing evidence that serum adipokine levels are associated with higher risks of cardiovascular diseases. As an important adipokine, fibroblast growth factor 21 (FGF21) has been demonstrated to be associated with atherosclerosis and coronary artery disease (CAD). However, circulating level of FGF21 in patients with angina pectoris has not yet been investigated. Circulating FGF21 level was examined in 197 patients with stable angina pectoris (SAP, n=66), unstable angina pectoris (UAP, n=76), and control subjects (n=55) along with clinical variables of cardiovascular risk factors. Serum FGF21 concentrations on admission were significantly increased more in patients with UAP than those with SAP (Ln-FGF21: 5.26 ± 0.87 compared with 4.85 ± 0.77, P<0.05) and control subjects (natural logarithm (Ln)-FGF21: 5.26 ± 0.87 compared with 4.54 ± 0.72, P<0.01). The correlation analysis revealed that serum FGF21 concentration was positively correlated with the levels of cardiac troponin I (cTnI) (r(2) = 0.026, P=0.027) and creatine kinase-MB (CK-MB) (r(2) = 0.023, P= 0.04). Furthermore, FGF21 level was identified as an independent factor associated with the risks of UAP (odds ratio (OR): 2.781; 95% CI: 1.476–5.239; P=0.002), after adjusting for gender, age, and body mass index (BMI). However, there were no correlations between serum FGF21 levels and the presence of SAP (OR: 1.248; 95% CI: 0.703–2.215; P=0.448). The present study indicates that FGF21 has a strong correlation and precise predictability for increased risks of UAP, that is independent of traditional risk factors of angina pectoris. Portland Press Ltd. 2018-09-25 /pmc/articles/PMC6153373/ /pubmed/30185439 http://dx.doi.org/10.1042/BSR20181099 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles Cheng, Jing Su, Xing Qiao, Lei Zhai, Chungang Chen, Wenqiang Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title | Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title_full | Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title_fullStr | Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title_full_unstemmed | Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title_short | Circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
title_sort | circulating level of fibroblast growth factor 21 is independently associated with the risks of unstable angina pectoris |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153373/ https://www.ncbi.nlm.nih.gov/pubmed/30185439 http://dx.doi.org/10.1042/BSR20181099 |
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