Cargando…
Circulating CD14(+) monocytes in patients with aortic stenosis
BACKGROUND: Calcific aortic stenosis (AS) is an active process sharing similarities with atherosclerosis and chronic inflammation. The pathophysiology of AS is notable for three cardinal components: inflammation, fibrosis and calcification. Monocytes play a role in each of these processes. The role...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753017/ https://www.ncbi.nlm.nih.gov/pubmed/26918018 http://dx.doi.org/10.11909/j.issn.1671-5411.2016.01.015 |
_version_ | 1782415819472371712 |
---|---|
author | Shimoni, Sara Meledin, Valery Bar, Iris Fabricant, Jacob Gandelman, Gera George, Jacob |
author_facet | Shimoni, Sara Meledin, Valery Bar, Iris Fabricant, Jacob Gandelman, Gera George, Jacob |
author_sort | Shimoni, Sara |
collection | PubMed |
description | BACKGROUND: Calcific aortic stenosis (AS) is an active process sharing similarities with atherosclerosis and chronic inflammation. The pathophysiology of AS is notable for three cardinal components: inflammation, fibrosis and calcification. Monocytes play a role in each of these processes. The role of circulating monocytes in AS is not clear. The aim of the present study was to study an association between circulating apoptotic and non apoptotic CD14(+) monocytes and AS features. METHODS: We assessed the number of CD14(+) monocytes and apoptotic monocytes in 54 patients with significant AS (aortic valve area 0.74 ± 0.27 cm(2)) and compared them to 33 patients with similar risk factors and no valvular disease. The level of CD14(+) monocytes and apoptotic monocytes was assessed by flow cytometry. RESULTS: There was no difference in the risk factor profile and known coronary or peripheral vascular diseases between patients with AS and controls. Patients with AS exhibited increased numbers of CD14(+) monocytes as compared to controls (9.9% ± 4.9% vs. 7.7% ± 3.9%, P = 0.03). CD14(+) monocyte number was related to age and the presence and severity of AS. In patients with AS, both CD14(+) monocytes and apoptotic monocytes were inversely related to aortic valve area. CONCLUSIONS: Patients with significant AS have increased number of circulating CD14(+) monocytes and there is an inverse correlation between monocyte count and aortic valve area. These findings may suggest that inflammation is operative not only in early valve injury phase, but also at later developed stages such as calcification when AS is severe. |
format | Online Article Text |
id | pubmed-4753017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47530172016-02-25 Circulating CD14(+) monocytes in patients with aortic stenosis Shimoni, Sara Meledin, Valery Bar, Iris Fabricant, Jacob Gandelman, Gera George, Jacob J Geriatr Cardiol Research Article BACKGROUND: Calcific aortic stenosis (AS) is an active process sharing similarities with atherosclerosis and chronic inflammation. The pathophysiology of AS is notable for three cardinal components: inflammation, fibrosis and calcification. Monocytes play a role in each of these processes. The role of circulating monocytes in AS is not clear. The aim of the present study was to study an association between circulating apoptotic and non apoptotic CD14(+) monocytes and AS features. METHODS: We assessed the number of CD14(+) monocytes and apoptotic monocytes in 54 patients with significant AS (aortic valve area 0.74 ± 0.27 cm(2)) and compared them to 33 patients with similar risk factors and no valvular disease. The level of CD14(+) monocytes and apoptotic monocytes was assessed by flow cytometry. RESULTS: There was no difference in the risk factor profile and known coronary or peripheral vascular diseases between patients with AS and controls. Patients with AS exhibited increased numbers of CD14(+) monocytes as compared to controls (9.9% ± 4.9% vs. 7.7% ± 3.9%, P = 0.03). CD14(+) monocyte number was related to age and the presence and severity of AS. In patients with AS, both CD14(+) monocytes and apoptotic monocytes were inversely related to aortic valve area. CONCLUSIONS: Patients with significant AS have increased number of circulating CD14(+) monocytes and there is an inverse correlation between monocyte count and aortic valve area. These findings may suggest that inflammation is operative not only in early valve injury phase, but also at later developed stages such as calcification when AS is severe. Science Press 2016-01 /pmc/articles/PMC4753017/ /pubmed/26918018 http://dx.doi.org/10.11909/j.issn.1671-5411.2016.01.015 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 Shimoni, Sara Meledin, Valery Bar, Iris Fabricant, Jacob Gandelman, Gera George, Jacob Circulating CD14(+) monocytes in patients with aortic stenosis |
title | Circulating CD14(+) monocytes in patients with aortic stenosis |
title_full | Circulating CD14(+) monocytes in patients with aortic stenosis |
title_fullStr | Circulating CD14(+) monocytes in patients with aortic stenosis |
title_full_unstemmed | Circulating CD14(+) monocytes in patients with aortic stenosis |
title_short | Circulating CD14(+) monocytes in patients with aortic stenosis |
title_sort | circulating cd14(+) monocytes in patients with aortic stenosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753017/ https://www.ncbi.nlm.nih.gov/pubmed/26918018 http://dx.doi.org/10.11909/j.issn.1671-5411.2016.01.015 |
work_keys_str_mv | AT shimonisara circulatingcd14monocytesinpatientswithaorticstenosis AT meledinvalery circulatingcd14monocytesinpatientswithaorticstenosis AT bariris circulatingcd14monocytesinpatientswithaorticstenosis AT fabricantjacob circulatingcd14monocytesinpatientswithaorticstenosis AT gandelmangera circulatingcd14monocytesinpatientswithaorticstenosis AT georgejacob circulatingcd14monocytesinpatientswithaorticstenosis |