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Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease

BACKGROUND: Calcific aortic valve disease (CAVD) is a slowly progressive pathologic process associated with significant morbidity and mortality, CAVD is the most common valve heart disease in the elderly and a leading cause of aortic valve stenosis. Multiple steps characterize the process: inflammat...

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Autores principales: Fu, Bo, Zhang, Yuhui, Chen, Qingliang, Guo, Zhigang, Jiang, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333163/
https://www.ncbi.nlm.nih.gov/pubmed/32647686
http://dx.doi.org/10.21037/atm-20-4463
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author Fu, Bo
Zhang, Yuhui
Chen, Qingliang
Guo, Zhigang
Jiang, Nan
author_facet Fu, Bo
Zhang, Yuhui
Chen, Qingliang
Guo, Zhigang
Jiang, Nan
author_sort Fu, Bo
collection PubMed
description BACKGROUND: Calcific aortic valve disease (CAVD) is a slowly progressive pathologic process associated with significant morbidity and mortality, CAVD is the most common valve heart disease in the elderly and a leading cause of aortic valve stenosis. Multiple steps characterize the process: inflammation, cell apoptosis, lipid deposition, renin-angiotensin system activation, extracellular matrix remodeling, and bone formation. This paper focuses on detecting and analyzing the expression of serum inflammatory factors in CAVD by antibody microarray techniques. METHODS: In this study, a total of 258 patients were included at Tianjin Chest Hospital between January 2017 and December 2018, subjects were divided into three groups: control, coronary artery disease (CAD), and CAVD. Blood samples were collected, and adipokine/cytokine/chemokine serum profiles were measured by antibody arrays. RESULTS: These data suggest that B-Lymphocyte Chemoattractant (BLC), Interleukin (IL)-12p40, monokine inducible by γ interferon (MIG), and Macrophage inflammatory protein (MIP)-1delta were significantly increased in CAVD compared to control or CAD. Furthermore, Real-time quantified PCR, Western blot assay, and Flow cytometer detection showed that these four cytokines/chemokines were from peripheral blood mononuclear cells. CONCLUSIONS: These findings suggest that BLC, IL-12p40, MIG, and MIP-1delta can be used as a marker to assess CAVD, which could have significant clinical implications.
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spelling pubmed-73331632020-07-08 Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease Fu, Bo Zhang, Yuhui Chen, Qingliang Guo, Zhigang Jiang, Nan Ann Transl Med Original Article BACKGROUND: Calcific aortic valve disease (CAVD) is a slowly progressive pathologic process associated with significant morbidity and mortality, CAVD is the most common valve heart disease in the elderly and a leading cause of aortic valve stenosis. Multiple steps characterize the process: inflammation, cell apoptosis, lipid deposition, renin-angiotensin system activation, extracellular matrix remodeling, and bone formation. This paper focuses on detecting and analyzing the expression of serum inflammatory factors in CAVD by antibody microarray techniques. METHODS: In this study, a total of 258 patients were included at Tianjin Chest Hospital between January 2017 and December 2018, subjects were divided into three groups: control, coronary artery disease (CAD), and CAVD. Blood samples were collected, and adipokine/cytokine/chemokine serum profiles were measured by antibody arrays. RESULTS: These data suggest that B-Lymphocyte Chemoattractant (BLC), Interleukin (IL)-12p40, monokine inducible by γ interferon (MIG), and Macrophage inflammatory protein (MIP)-1delta were significantly increased in CAVD compared to control or CAD. Furthermore, Real-time quantified PCR, Western blot assay, and Flow cytometer detection showed that these four cytokines/chemokines were from peripheral blood mononuclear cells. CONCLUSIONS: These findings suggest that BLC, IL-12p40, MIG, and MIP-1delta can be used as a marker to assess CAVD, which could have significant clinical implications. AME Publishing Company 2020-06 /pmc/articles/PMC7333163/ /pubmed/32647686 http://dx.doi.org/10.21037/atm-20-4463 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Fu, Bo
Zhang, Yuhui
Chen, Qingliang
Guo, Zhigang
Jiang, Nan
Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title_full Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title_fullStr Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title_full_unstemmed Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title_short Antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
title_sort antibody microarray analysis of serum inflammatory cytokines in patients with calcific aortic valve disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333163/
https://www.ncbi.nlm.nih.gov/pubmed/32647686
http://dx.doi.org/10.21037/atm-20-4463
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