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Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction
OBJECTIVE: The occurrence of cardiovascular adverse events in the first year after ST-acute myocardial infarction (STEMI) remains high; therefore, identification of patients with poor prognosis is essential for early intervention. This study aimed to evaluate the prognostic value of metabolomics-bas...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667794/ https://www.ncbi.nlm.nih.gov/pubmed/36405744 http://dx.doi.org/10.3389/fimmu.2022.950441 |
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author | Zhang, Xiaolin Cai, Yi Su, Xu Jing, Quanmin Liu, Haiwei Na, Kun Qiu, Miaohan Tian, Xiaoxiang Liu, Dan Wu, Tianxiao Yan, Chenghui Han, Yaling |
author_facet | Zhang, Xiaolin Cai, Yi Su, Xu Jing, Quanmin Liu, Haiwei Na, Kun Qiu, Miaohan Tian, Xiaoxiang Liu, Dan Wu, Tianxiao Yan, Chenghui Han, Yaling |
author_sort | Zhang, Xiaolin |
collection | PubMed |
description | OBJECTIVE: The occurrence of cardiovascular adverse events in the first year after ST-acute myocardial infarction (STEMI) remains high; therefore, identification of patients with poor prognosis is essential for early intervention. This study aimed to evaluate the prognostic value of metabolomics-based biomarkers in STEMI patients and explore their functional mechanisms. METHODS: Metabolite profiling was performed using nuclear magnetic resonance. The plasma concentration of Kynurenine (Kyn) was measured using ultraperformance liquid chromatography/electrospray ionization quadruple time-of-flight mass spectrometry. Major adverse cardiac and cerebral events were assessed for 1 year. A functional metabolomics strategy was proposed for investigating the role of Kyn in both vitro and vivo models. RESULTS: The adjusted hazard ratios in STEMI patients for Kyn in the 4(th) quartile 7.12(5.71-10.82) was significantly higher than that in the 3(rd) quartile 3.03(2.62-3.74), 2(nd) quartile 1.86(1.70-2.03), and 1(st) quartile 1.20(0.93-1.39).The incidence of MACCE was significantly different among Kyn quartiles and the highest incidence of MACCE was observed in the 4th quartile when compared with the 1st quartile (9.84% vs.2.85%, P<0.001).Immunofluorescence staining indicated that indoleamine-pyrrole 2,3-dioxygenase (IDO1) was located in the CD68 positive staining area of thrombi from STEMI patients and Kyn was induced in the early phase after myocardial infarction. Kyn could trigger inflammation and oxidative stress of macrophage cells by activation of the Sirt3-acSOD2/IL-1β signaling pathway in vitro. CONCLUSIONS: Plasma Kyn levels were positively associated with the occurrence of STEMI. Kyn could induce macrophage cells inflammation and oxidative stress by activating the Sirt3-acSOD2/IL-1β pathway following myocardial ischemia injury. Kyn could be a robust biomarker for STEMI prognosis and reduction of Kyn could be beneficial in STEMI patients. |
format | Online Article Text |
id | pubmed-9667794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96677942022-11-17 Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction Zhang, Xiaolin Cai, Yi Su, Xu Jing, Quanmin Liu, Haiwei Na, Kun Qiu, Miaohan Tian, Xiaoxiang Liu, Dan Wu, Tianxiao Yan, Chenghui Han, Yaling Front Immunol Immunology OBJECTIVE: The occurrence of cardiovascular adverse events in the first year after ST-acute myocardial infarction (STEMI) remains high; therefore, identification of patients with poor prognosis is essential for early intervention. This study aimed to evaluate the prognostic value of metabolomics-based biomarkers in STEMI patients and explore their functional mechanisms. METHODS: Metabolite profiling was performed using nuclear magnetic resonance. The plasma concentration of Kynurenine (Kyn) was measured using ultraperformance liquid chromatography/electrospray ionization quadruple time-of-flight mass spectrometry. Major adverse cardiac and cerebral events were assessed for 1 year. A functional metabolomics strategy was proposed for investigating the role of Kyn in both vitro and vivo models. RESULTS: The adjusted hazard ratios in STEMI patients for Kyn in the 4(th) quartile 7.12(5.71-10.82) was significantly higher than that in the 3(rd) quartile 3.03(2.62-3.74), 2(nd) quartile 1.86(1.70-2.03), and 1(st) quartile 1.20(0.93-1.39).The incidence of MACCE was significantly different among Kyn quartiles and the highest incidence of MACCE was observed in the 4th quartile when compared with the 1st quartile (9.84% vs.2.85%, P<0.001).Immunofluorescence staining indicated that indoleamine-pyrrole 2,3-dioxygenase (IDO1) was located in the CD68 positive staining area of thrombi from STEMI patients and Kyn was induced in the early phase after myocardial infarction. Kyn could trigger inflammation and oxidative stress of macrophage cells by activation of the Sirt3-acSOD2/IL-1β signaling pathway in vitro. CONCLUSIONS: Plasma Kyn levels were positively associated with the occurrence of STEMI. Kyn could induce macrophage cells inflammation and oxidative stress by activating the Sirt3-acSOD2/IL-1β pathway following myocardial ischemia injury. Kyn could be a robust biomarker for STEMI prognosis and reduction of Kyn could be beneficial in STEMI patients. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9667794/ /pubmed/36405744 http://dx.doi.org/10.3389/fimmu.2022.950441 Text en Copyright © 2022 Zhang, Cai, Su, Jing, Liu, Na, Qiu, Tian, Liu, Wu, Yan and Han https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zhang, Xiaolin Cai, Yi Su, Xu Jing, Quanmin Liu, Haiwei Na, Kun Qiu, Miaohan Tian, Xiaoxiang Liu, Dan Wu, Tianxiao Yan, Chenghui Han, Yaling Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title | Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title_full | Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title_fullStr | Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title_full_unstemmed | Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title_short | Untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
title_sort | untargeted metabolomics identified kynurenine as a predictive prognostic biomarker in acute myocardial infarction |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667794/ https://www.ncbi.nlm.nih.gov/pubmed/36405744 http://dx.doi.org/10.3389/fimmu.2022.950441 |
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