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Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study

BACKGROUND: Decreased levels of circulating bone marrow-derived progenitor cells have been associated with risk factors and cardiovascular diseases. Smoking is the most important modifiable risk factor for atherosclerosis in young women. The aim of this pilot study was to assess in healthy premenopa...

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Autores principales: Ludwig, Antje, Jochmann, Nicoline, Kertesz, Andras, Kuhn, Claudia, Mueller, Simone, Gericke, Christine, Baumann, Gert, Stangl, Karl, Stangl, Verena
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891626/
https://www.ncbi.nlm.nih.gov/pubmed/20509965
http://dx.doi.org/10.1186/1472-6874-10-20
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author Ludwig, Antje
Jochmann, Nicoline
Kertesz, Andras
Kuhn, Claudia
Mueller, Simone
Gericke, Christine
Baumann, Gert
Stangl, Karl
Stangl, Verena
author_facet Ludwig, Antje
Jochmann, Nicoline
Kertesz, Andras
Kuhn, Claudia
Mueller, Simone
Gericke, Christine
Baumann, Gert
Stangl, Karl
Stangl, Verena
author_sort Ludwig, Antje
collection PubMed
description BACKGROUND: Decreased levels of circulating bone marrow-derived progenitor cells have been associated with risk factors and cardiovascular diseases. Smoking is the most important modifiable risk factor for atherosclerosis in young women. The aim of this pilot study was to assess in healthy premenopausal women without other risk factors for cardiovascular disease the influence of nicotine abuse on the number of circulating progenitor cells in relation to endothelial function. METHODS: The number of endothelial progenitor cells, measured as colony-forming units in a cell-culture assay (EPC-CFU) and the number of circulating CD34 + and CD34 + /CD133 + cells, measured by flow cytometry, was estimated in 32 women at the menstrual phase of the menstrual cycle. In addition, flow-mediated dilation (FMD) was assessed as a marker for vascular function. In a subgroup of these women (n = 20), progenitor cells were also investigated at the mid-follicular and luteal phases of the menstrual cycle. RESULTS: Compared to non-smokers, the abundance of circulating CD34 + cells was significantly lower in smoking women in the menstrual, mid-luteal, and mid-follicular phases of the menstrual cycle. The number of CD34 + progenitor cells was revealed to have significant positive correlation with FMD in young healthy women, whereas CD34 + /CD133 + progenitor cells and EPC-CFU showed no significant correlation. CONCLUSION: The number of CD34 + progenitor cells positively correlates with FMD in young healthy women and is decreased by smoking.
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spelling pubmed-28916262010-06-25 Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study Ludwig, Antje Jochmann, Nicoline Kertesz, Andras Kuhn, Claudia Mueller, Simone Gericke, Christine Baumann, Gert Stangl, Karl Stangl, Verena BMC Womens Health Research article BACKGROUND: Decreased levels of circulating bone marrow-derived progenitor cells have been associated with risk factors and cardiovascular diseases. Smoking is the most important modifiable risk factor for atherosclerosis in young women. The aim of this pilot study was to assess in healthy premenopausal women without other risk factors for cardiovascular disease the influence of nicotine abuse on the number of circulating progenitor cells in relation to endothelial function. METHODS: The number of endothelial progenitor cells, measured as colony-forming units in a cell-culture assay (EPC-CFU) and the number of circulating CD34 + and CD34 + /CD133 + cells, measured by flow cytometry, was estimated in 32 women at the menstrual phase of the menstrual cycle. In addition, flow-mediated dilation (FMD) was assessed as a marker for vascular function. In a subgroup of these women (n = 20), progenitor cells were also investigated at the mid-follicular and luteal phases of the menstrual cycle. RESULTS: Compared to non-smokers, the abundance of circulating CD34 + cells was significantly lower in smoking women in the menstrual, mid-luteal, and mid-follicular phases of the menstrual cycle. The number of CD34 + progenitor cells was revealed to have significant positive correlation with FMD in young healthy women, whereas CD34 + /CD133 + progenitor cells and EPC-CFU showed no significant correlation. CONCLUSION: The number of CD34 + progenitor cells positively correlates with FMD in young healthy women and is decreased by smoking. BioMed Central 2010-05-30 /pmc/articles/PMC2891626/ /pubmed/20509965 http://dx.doi.org/10.1186/1472-6874-10-20 Text en Copyright ©2010 Ludwig et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Ludwig, Antje
Jochmann, Nicoline
Kertesz, Andras
Kuhn, Claudia
Mueller, Simone
Gericke, Christine
Baumann, Gert
Stangl, Karl
Stangl, Verena
Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title_full Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title_fullStr Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title_full_unstemmed Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title_short Smoking decreases the level of circulating CD34+ progenitor cells in young healthy women - a pilot study
title_sort smoking decreases the level of circulating cd34+ progenitor cells in young healthy women - a pilot study
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891626/
https://www.ncbi.nlm.nih.gov/pubmed/20509965
http://dx.doi.org/10.1186/1472-6874-10-20
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