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Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis

Fulminant myocarditis (FM) is the severest type of myocarditis and requires timely diagnosis and treatment. However, effective biomarkers for early diagnosis of FM are limited. First, 12 common inflammatory cytokines levels in the plasma of patients with FM were measured using human cytokine 12-Plex...

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Autores principales: Zhuang, Yan, Wang, Jin, Li, Huihui, Chen, Yanghui, Chen, Chen, Wang, Dao Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687192/
https://www.ncbi.nlm.nih.gov/pubmed/36428509
http://dx.doi.org/10.3390/biomedicines10112941
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author Zhuang, Yan
Wang, Jin
Li, Huihui
Chen, Yanghui
Chen, Chen
Wang, Dao Wen
author_facet Zhuang, Yan
Wang, Jin
Li, Huihui
Chen, Yanghui
Chen, Chen
Wang, Dao Wen
author_sort Zhuang, Yan
collection PubMed
description Fulminant myocarditis (FM) is the severest type of myocarditis and requires timely diagnosis and treatment. However, effective biomarkers for early diagnosis of FM are limited. First, 12 common inflammatory cytokines levels in the plasma of patients with FM were measured using human cytokine 12-Plex assay. Then, enzyme-linked immunosorbent assay (ELISA) was used to detect the plasma levels of another eight cytokines that we previously reported on. Moreover, a Spearman correlation test was employed to investigate the correlations between the plasma cytokine levels and the clinical parameters of patients with FM. Finally, receiver operating characteristic (ROC) curve analyses were performed to assess the diagnostic performance of plasma cytokine levels for the detection of FM. Five of the twelve common inflammation cytokines were significantly altered in patients with FM, but none of them was correlated with the severity of FM. Six of the eight significantly changed cytokines that we previously reported on were validated by ELISA. Among these, sST2, Siglec-5, and CD163 were negatively correlated with ejection fraction values. Furthermore, plasma Siglec-5 and CD163 levels were found to be associated with the severity of FM. Finally, both plasma Siglec-5 and CD163 showed outstanding diagnostic performance for FM. The current study identified plasma Siglec-5 and CD163 as valuable novel biomarkers for the early diagnosis of FM.
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spelling pubmed-96871922022-11-25 Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis Zhuang, Yan Wang, Jin Li, Huihui Chen, Yanghui Chen, Chen Wang, Dao Wen Biomedicines Article Fulminant myocarditis (FM) is the severest type of myocarditis and requires timely diagnosis and treatment. However, effective biomarkers for early diagnosis of FM are limited. First, 12 common inflammatory cytokines levels in the plasma of patients with FM were measured using human cytokine 12-Plex assay. Then, enzyme-linked immunosorbent assay (ELISA) was used to detect the plasma levels of another eight cytokines that we previously reported on. Moreover, a Spearman correlation test was employed to investigate the correlations between the plasma cytokine levels and the clinical parameters of patients with FM. Finally, receiver operating characteristic (ROC) curve analyses were performed to assess the diagnostic performance of plasma cytokine levels for the detection of FM. Five of the twelve common inflammation cytokines were significantly altered in patients with FM, but none of them was correlated with the severity of FM. Six of the eight significantly changed cytokines that we previously reported on were validated by ELISA. Among these, sST2, Siglec-5, and CD163 were negatively correlated with ejection fraction values. Furthermore, plasma Siglec-5 and CD163 levels were found to be associated with the severity of FM. Finally, both plasma Siglec-5 and CD163 showed outstanding diagnostic performance for FM. The current study identified plasma Siglec-5 and CD163 as valuable novel biomarkers for the early diagnosis of FM. MDPI 2022-11-15 /pmc/articles/PMC9687192/ /pubmed/36428509 http://dx.doi.org/10.3390/biomedicines10112941 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhuang, Yan
Wang, Jin
Li, Huihui
Chen, Yanghui
Chen, Chen
Wang, Dao Wen
Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title_full Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title_fullStr Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title_full_unstemmed Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title_short Plasma Siglec-5 and CD163 as Novel Biomarkers for Fulminant Myocarditis
title_sort plasma siglec-5 and cd163 as novel biomarkers for fulminant myocarditis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687192/
https://www.ncbi.nlm.nih.gov/pubmed/36428509
http://dx.doi.org/10.3390/biomedicines10112941
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