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Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction
BACKGROUND: Visfatin is an adipokine that related with the inflammation in atherosclerosis and the destabilization of atherosclerotic plaque. The aim of this study was to observe the relationship between visfatin and major adverse cardiovascular events (MACEs) in acute myocardial infarction (AMI) pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275306/ https://www.ncbi.nlm.nih.gov/pubmed/32503436 http://dx.doi.org/10.1186/s12872-020-01549-3 |
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author | Zheng, Meifan Lu, Nan Ren, Meixia Chen, Haifeng |
author_facet | Zheng, Meifan Lu, Nan Ren, Meixia Chen, Haifeng |
author_sort | Zheng, Meifan |
collection | PubMed |
description | BACKGROUND: Visfatin is an adipokine that related with the inflammation in atherosclerosis and the destabilization of atherosclerotic plaque. The aim of this study was to observe the relationship between visfatin and major adverse cardiovascular events (MACEs) in acute myocardial infarction (AMI) patients. METHODS: We enrolled a total of 238 patients (183 AMI and 55 control) who underwent coronary angiography. Patients with AMI were followed for an average of 19.3 months and 159 patients were finally included in the study. RESULTS: It was observed patients with AMI had higher serum visfatin levels than controls. The total incidence of MACEs was 11.32% (18/159) in AMI patients. After calculation of the Youden index, the best cut-off value of visfatin on the curve of receiver-operating characteristic was 8.799 ng/mL for predicting the occurrence of MACEs. The occurrence of MACEs was elevated in high-visfatin group (≥8.799 ng/mL) compared with low-visfatin group (≤8.799 ng/mL). The time to MACEs was correlated with visfatin (HR = 1.235, 95%CI 1.051–1.451, P = 0.01) and high-visfatin group had an earlier time to MACEs and a shorter time of cumulative survival. CONCLUSIONS: Increased serum visfatin levels were observed in AMI patients, and correlated with an earlier onset and higher incidence of MACEs. |
format | Online Article Text |
id | pubmed-7275306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72753062020-06-08 Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction Zheng, Meifan Lu, Nan Ren, Meixia Chen, Haifeng BMC Cardiovasc Disord Research Article BACKGROUND: Visfatin is an adipokine that related with the inflammation in atherosclerosis and the destabilization of atherosclerotic plaque. The aim of this study was to observe the relationship between visfatin and major adverse cardiovascular events (MACEs) in acute myocardial infarction (AMI) patients. METHODS: We enrolled a total of 238 patients (183 AMI and 55 control) who underwent coronary angiography. Patients with AMI were followed for an average of 19.3 months and 159 patients were finally included in the study. RESULTS: It was observed patients with AMI had higher serum visfatin levels than controls. The total incidence of MACEs was 11.32% (18/159) in AMI patients. After calculation of the Youden index, the best cut-off value of visfatin on the curve of receiver-operating characteristic was 8.799 ng/mL for predicting the occurrence of MACEs. The occurrence of MACEs was elevated in high-visfatin group (≥8.799 ng/mL) compared with low-visfatin group (≤8.799 ng/mL). The time to MACEs was correlated with visfatin (HR = 1.235, 95%CI 1.051–1.451, P = 0.01) and high-visfatin group had an earlier time to MACEs and a shorter time of cumulative survival. CONCLUSIONS: Increased serum visfatin levels were observed in AMI patients, and correlated with an earlier onset and higher incidence of MACEs. BioMed Central 2020-06-05 /pmc/articles/PMC7275306/ /pubmed/32503436 http://dx.doi.org/10.1186/s12872-020-01549-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Zheng, Meifan Lu, Nan Ren, Meixia Chen, Haifeng Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title | Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title_full | Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title_fullStr | Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title_full_unstemmed | Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title_short | Visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
title_sort | visfatin associated with major adverse cardiovascular events in patients with acute myocardial infarction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275306/ https://www.ncbi.nlm.nih.gov/pubmed/32503436 http://dx.doi.org/10.1186/s12872-020-01549-3 |
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