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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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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. |
format | Online Article Text |
id | pubmed-7333163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
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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