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Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction

Importance: S100A12 is a calcium binding protein which is involved in inflammation and progression of atherosclerosis. Objective: We sought to investigate the utility of S100A12 as a biomarker for the early diagnosis and prognostication of patients presenting with ST-segment elevation myocardial inf...

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Autores principales: Zhang, Xiaolin, Cheng, Minghui, Gao, Naijing, Li, Yi, Yan, Chenghui, Tian, Xiaoxiang, Liu, Dan, Qiu, Miaohan, Wang, Xiaozeng, Luan, Bo, Deng, Jie, Wang, Shouli, Tian, Hongyan, Wang, Geng, Ma, Xinliang, Stone, Gregg W., Han, Yaling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718434/
https://www.ncbi.nlm.nih.gov/pubmed/34977174
http://dx.doi.org/10.3389/fcvm.2021.747511
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author Zhang, Xiaolin
Cheng, Minghui
Gao, Naijing
Li, Yi
Yan, Chenghui
Tian, Xiaoxiang
Liu, Dan
Qiu, Miaohan
Wang, Xiaozeng
Luan, Bo
Deng, Jie
Wang, Shouli
Tian, Hongyan
Wang, Geng
Ma, Xinliang
Stone, Gregg W.
Han, Yaling
author_facet Zhang, Xiaolin
Cheng, Minghui
Gao, Naijing
Li, Yi
Yan, Chenghui
Tian, Xiaoxiang
Liu, Dan
Qiu, Miaohan
Wang, Xiaozeng
Luan, Bo
Deng, Jie
Wang, Shouli
Tian, Hongyan
Wang, Geng
Ma, Xinliang
Stone, Gregg W.
Han, Yaling
author_sort Zhang, Xiaolin
collection PubMed
description Importance: S100A12 is a calcium binding protein which is involved in inflammation and progression of atherosclerosis. Objective: We sought to investigate the utility of S100A12 as a biomarker for the early diagnosis and prognostication of patients presenting with ST-segment elevation myocardial infarction (STEMI). Design, Setting, and Participants: S100A12 was measured in 1023 patients presenting to the emergency department with acute chest pain between June 2012 and November 2015. An independent cohort of 398 patients enrolled at 3 different hospitals served as a validation cohort. Main Outcomes and Measures: The primary clinical endpoint of interest was major adverse cardiac and cerebral events (MACCE) defined as a composite of all-cause death, MI, stroke, or hospitalization for heart failure. Results: A total of 438/1023 patients (42.8%) in the diagnosis cohort were adjudicated as STEMI, among whom plasma S100A12 levels increased within 30 min and peaked 1–2 h after symptom onset. Compared with high-sensitivity cardiac troponin T and creatine kinase-MB isoenzyme, S100A12 more accurately identified STEMI, especially within the first 2 h after symptom onset (area under the curve 0.963 compared with 0.860 for hscTnT and 0.711 for CK-MB, both P < 0.05). These results were consistent in the 243-patient validation cohort. The 1-year rate of MACCE was greatest in patients in the highest peak S100A12 tertile, intermediate in the middle tertile and least in the lowest tertile (9.3 vs. 5.7 vs. 3.0% respectively, P(trend) = 0.0006). By multivariable analysis the peak plasma concentration of S100A12 was an independent predictor of MACCE within 1 year after STEMI (HR, 1.001, 95%CI, 1.000–1.002; P = 0.0104). Conclusions and Relevance: S100A12 rapidly identified patients with STEMI, more accurately than other cardiac biomarkers, especially within the first 2 h after symptom onset. The peak plasma S100A12 level was a strong predictor of 1-year prognosis after STEMI.
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spelling pubmed-87184342022-01-01 Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction Zhang, Xiaolin Cheng, Minghui Gao, Naijing Li, Yi Yan, Chenghui Tian, Xiaoxiang Liu, Dan Qiu, Miaohan Wang, Xiaozeng Luan, Bo Deng, Jie Wang, Shouli Tian, Hongyan Wang, Geng Ma, Xinliang Stone, Gregg W. Han, Yaling Front Cardiovasc Med Cardiovascular Medicine Importance: S100A12 is a calcium binding protein which is involved in inflammation and progression of atherosclerosis. Objective: We sought to investigate the utility of S100A12 as a biomarker for the early diagnosis and prognostication of patients presenting with ST-segment elevation myocardial infarction (STEMI). Design, Setting, and Participants: S100A12 was measured in 1023 patients presenting to the emergency department with acute chest pain between June 2012 and November 2015. An independent cohort of 398 patients enrolled at 3 different hospitals served as a validation cohort. Main Outcomes and Measures: The primary clinical endpoint of interest was major adverse cardiac and cerebral events (MACCE) defined as a composite of all-cause death, MI, stroke, or hospitalization for heart failure. Results: A total of 438/1023 patients (42.8%) in the diagnosis cohort were adjudicated as STEMI, among whom plasma S100A12 levels increased within 30 min and peaked 1–2 h after symptom onset. Compared with high-sensitivity cardiac troponin T and creatine kinase-MB isoenzyme, S100A12 more accurately identified STEMI, especially within the first 2 h after symptom onset (area under the curve 0.963 compared with 0.860 for hscTnT and 0.711 for CK-MB, both P < 0.05). These results were consistent in the 243-patient validation cohort. The 1-year rate of MACCE was greatest in patients in the highest peak S100A12 tertile, intermediate in the middle tertile and least in the lowest tertile (9.3 vs. 5.7 vs. 3.0% respectively, P(trend) = 0.0006). By multivariable analysis the peak plasma concentration of S100A12 was an independent predictor of MACCE within 1 year after STEMI (HR, 1.001, 95%CI, 1.000–1.002; P = 0.0104). Conclusions and Relevance: S100A12 rapidly identified patients with STEMI, more accurately than other cardiac biomarkers, especially within the first 2 h after symptom onset. The peak plasma S100A12 level was a strong predictor of 1-year prognosis after STEMI. Frontiers Media S.A. 2021-12-17 /pmc/articles/PMC8718434/ /pubmed/34977174 http://dx.doi.org/10.3389/fcvm.2021.747511 Text en Copyright © 2021 Zhang, Cheng, Gao, Li, Yan, Tian, Liu, Qiu, Wang, Luan, Deng, Wang, Tian, Wang, Ma, Stone 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 Cardiovascular Medicine
Zhang, Xiaolin
Cheng, Minghui
Gao, Naijing
Li, Yi
Yan, Chenghui
Tian, Xiaoxiang
Liu, Dan
Qiu, Miaohan
Wang, Xiaozeng
Luan, Bo
Deng, Jie
Wang, Shouli
Tian, Hongyan
Wang, Geng
Ma, Xinliang
Stone, Gregg W.
Han, Yaling
Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title_full Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title_fullStr Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title_full_unstemmed Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title_short Utility of S100A12 as an Early Biomarker in Patients With ST-Segment Elevation Myocardial Infarction
title_sort utility of s100a12 as an early biomarker in patients with st-segment elevation myocardial infarction
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718434/
https://www.ncbi.nlm.nih.gov/pubmed/34977174
http://dx.doi.org/10.3389/fcvm.2021.747511
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