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C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction

OBJECTIVE: To investigate whether C-reactive protein (CRP) is a biomarker of malignant ventricular arrhythmias (MVA) occurring in non-ST elevation myocardial infarction (NSTEMI) patients with Global Registry of Acute Coronary events (GRACE) scores < 140. METHODS: A total of 1450 NSTEMI patients w...

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Autores principales: Wang, Cheng-Gang, Qin, Xiu-Chuan, Nie, Shao-Ping, Wang, Chun-Mei, Ai, Hui, Que, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748903/
https://www.ncbi.nlm.nih.gov/pubmed/31555329
http://dx.doi.org/10.11909/j.issn.1671-5411.2019.08.007
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author Wang, Cheng-Gang
Qin, Xiu-Chuan
Nie, Shao-Ping
Wang, Chun-Mei
Ai, Hui
Que, Bin
author_facet Wang, Cheng-Gang
Qin, Xiu-Chuan
Nie, Shao-Ping
Wang, Chun-Mei
Ai, Hui
Que, Bin
author_sort Wang, Cheng-Gang
collection PubMed
description OBJECTIVE: To investigate whether C-reactive protein (CRP) is a biomarker of malignant ventricular arrhythmias (MVA) occurring in non-ST elevation myocardial infarction (NSTEMI) patients with Global Registry of Acute Coronary events (GRACE) scores < 140. METHODS: A total of 1450 NSTEMI patients were included in this study. Hs-CRP blood levels were measured via a turbidimetric immunoassay after confirming the diagnosis of NSTEMI with GRACE scores < 140. RESULTS: Consistent with prior studies, the MVA occurrence rate in our cohort was 6.7%, and patients with MVA exhibited a reduced left ventricular ejection fraction (46.1% ± 6.9% vs. 61.5% ± 8.7%, P = 0.032), a higher incidence of Killip classification > 1 (34.1% vs. 24.2%, P < 0.001), an increased surgical revascularization rate (34.1% vs. 9.7%, P < 0.001), and increased mortality (16.5% vs. 5.8%, P < 0.001). Serum hs-CRP levels were higher (P = 0.003) in NSTEMI patients with MVA, and this increase appeared unrelated to other clinical parameters. The C-statistic to discriminate MVA was 0.82 (95% CI: 0.74–0.89). Using receiver operating characteristics analysis, we optimized a cutoff point of 16 mL/L, and the sensitivity and specificity were 95% and 61%, respectively; the positive predictive value was 20% and the negative predictive value was 99%. CONCLUSIONS: An hs-CRP assay is a potential MVA biomarker in low-risk NSTEMI patients with GRACE scores < 140. If validated in prospective studies, hs-CRP may offer a low-cost supplementary strategy for risk stratification for NSTEMI patients.
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spelling pubmed-67489032019-09-25 C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction Wang, Cheng-Gang Qin, Xiu-Chuan Nie, Shao-Ping Wang, Chun-Mei Ai, Hui Que, Bin J Geriatr Cardiol Research Article OBJECTIVE: To investigate whether C-reactive protein (CRP) is a biomarker of malignant ventricular arrhythmias (MVA) occurring in non-ST elevation myocardial infarction (NSTEMI) patients with Global Registry of Acute Coronary events (GRACE) scores < 140. METHODS: A total of 1450 NSTEMI patients were included in this study. Hs-CRP blood levels were measured via a turbidimetric immunoassay after confirming the diagnosis of NSTEMI with GRACE scores < 140. RESULTS: Consistent with prior studies, the MVA occurrence rate in our cohort was 6.7%, and patients with MVA exhibited a reduced left ventricular ejection fraction (46.1% ± 6.9% vs. 61.5% ± 8.7%, P = 0.032), a higher incidence of Killip classification > 1 (34.1% vs. 24.2%, P < 0.001), an increased surgical revascularization rate (34.1% vs. 9.7%, P < 0.001), and increased mortality (16.5% vs. 5.8%, P < 0.001). Serum hs-CRP levels were higher (P = 0.003) in NSTEMI patients with MVA, and this increase appeared unrelated to other clinical parameters. The C-statistic to discriminate MVA was 0.82 (95% CI: 0.74–0.89). Using receiver operating characteristics analysis, we optimized a cutoff point of 16 mL/L, and the sensitivity and specificity were 95% and 61%, respectively; the positive predictive value was 20% and the negative predictive value was 99%. CONCLUSIONS: An hs-CRP assay is a potential MVA biomarker in low-risk NSTEMI patients with GRACE scores < 140. If validated in prospective studies, hs-CRP may offer a low-cost supplementary strategy for risk stratification for NSTEMI patients. Science Press 2019-08 /pmc/articles/PMC6748903/ /pubmed/31555329 http://dx.doi.org/10.11909/j.issn.1671-5411.2019.08.007 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Research Article
Wang, Cheng-Gang
Qin, Xiu-Chuan
Nie, Shao-Ping
Wang, Chun-Mei
Ai, Hui
Que, Bin
C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title_full C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title_fullStr C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title_full_unstemmed C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title_short C-reactive protein as a predictor of malignant ventricular arrhythmias in non-ST elevation myocardial infarction
title_sort c-reactive protein as a predictor of malignant ventricular arrhythmias in non-st elevation myocardial infarction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748903/
https://www.ncbi.nlm.nih.gov/pubmed/31555329
http://dx.doi.org/10.11909/j.issn.1671-5411.2019.08.007
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