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TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure

Patients with advanced heart failure (HF) have reduced cardiac output and impaired peripheral blood flow, which diminishes endothelial shear stress and consequently flow-mediated dilatation (FMD). The aim of our study was to find out whether endothelial dysfunction is associated with the number of C...

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Autores principales: Ugovšek, Sabina, Rehberger Likozar, Andreja, Finderle, Sanjo, Poglajen, Gregor, Okrajšek, Renata, Vrtovec, Bojan, Šebeštjen, Miran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410381/
https://www.ncbi.nlm.nih.gov/pubmed/36005445
http://dx.doi.org/10.3390/jcdd9080281
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author Ugovšek, Sabina
Rehberger Likozar, Andreja
Finderle, Sanjo
Poglajen, Gregor
Okrajšek, Renata
Vrtovec, Bojan
Šebeštjen, Miran
author_facet Ugovšek, Sabina
Rehberger Likozar, Andreja
Finderle, Sanjo
Poglajen, Gregor
Okrajšek, Renata
Vrtovec, Bojan
Šebeštjen, Miran
author_sort Ugovšek, Sabina
collection PubMed
description Patients with advanced heart failure (HF) have reduced cardiac output and impaired peripheral blood flow, which diminishes endothelial shear stress and consequently flow-mediated dilatation (FMD). The aim of our study was to find out whether endothelial dysfunction is associated with the number of CD34(+) cells and TNF-α levels in patients with ischemic and non-ischemic HF after stimulation with granulocyte colony-stimulating factor (G-CSF). We included 56 patients with advanced HF (LVEF < 35%). Eighteen patients (32.14%) had ischemic and 38 (67.86%) patients had non-ischemic HF. FMD of the brachial artery was performed before the patients underwent 5-day bone marrow stimulation with daily subcutaneous injections of G-CSF (5 μg/kg bid). On the fifth day peripheral blood CD34(+) cell count was measured. No statistically significant differences were found between the patient groups in NT-proBNP levels ((1575 (425–2439) vs. 1273 (225–2239)) pg/mL; p = 0.40), peripheral blood CD34(+) cell count ((67.54 ± 102.32 vs. 89.76 ± 71.21) × 10(6); p = 0.32), TNF-α ((8.72 ± 10.30 vs. 4.96 ± 6.16) ng/mL; p = 0.13) and FMD (6.7 ± 5.4 vs. 7.2 ± 5.9%; p = 0.76). In a linear regression model, only FMD (p = 0.001) and TNF-α (p = 0.003) emerged as statistically significant predictors of CD34(+) cells counts. Our study suggests that TNF-α is a good predictor of impaired endothelial function and of CD34(+) cells mobilization after G-CSF stimulation in patients with advanced HF of ischemic and non-ischemic origin.
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spelling pubmed-94103812022-08-26 TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure Ugovšek, Sabina Rehberger Likozar, Andreja Finderle, Sanjo Poglajen, Gregor Okrajšek, Renata Vrtovec, Bojan Šebeštjen, Miran J Cardiovasc Dev Dis Article Patients with advanced heart failure (HF) have reduced cardiac output and impaired peripheral blood flow, which diminishes endothelial shear stress and consequently flow-mediated dilatation (FMD). The aim of our study was to find out whether endothelial dysfunction is associated with the number of CD34(+) cells and TNF-α levels in patients with ischemic and non-ischemic HF after stimulation with granulocyte colony-stimulating factor (G-CSF). We included 56 patients with advanced HF (LVEF < 35%). Eighteen patients (32.14%) had ischemic and 38 (67.86%) patients had non-ischemic HF. FMD of the brachial artery was performed before the patients underwent 5-day bone marrow stimulation with daily subcutaneous injections of G-CSF (5 μg/kg bid). On the fifth day peripheral blood CD34(+) cell count was measured. No statistically significant differences were found between the patient groups in NT-proBNP levels ((1575 (425–2439) vs. 1273 (225–2239)) pg/mL; p = 0.40), peripheral blood CD34(+) cell count ((67.54 ± 102.32 vs. 89.76 ± 71.21) × 10(6); p = 0.32), TNF-α ((8.72 ± 10.30 vs. 4.96 ± 6.16) ng/mL; p = 0.13) and FMD (6.7 ± 5.4 vs. 7.2 ± 5.9%; p = 0.76). In a linear regression model, only FMD (p = 0.001) and TNF-α (p = 0.003) emerged as statistically significant predictors of CD34(+) cells counts. Our study suggests that TNF-α is a good predictor of impaired endothelial function and of CD34(+) cells mobilization after G-CSF stimulation in patients with advanced HF of ischemic and non-ischemic origin. MDPI 2022-08-20 /pmc/articles/PMC9410381/ /pubmed/36005445 http://dx.doi.org/10.3390/jcdd9080281 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
Ugovšek, Sabina
Rehberger Likozar, Andreja
Finderle, Sanjo
Poglajen, Gregor
Okrajšek, Renata
Vrtovec, Bojan
Šebeštjen, Miran
TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title_full TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title_fullStr TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title_full_unstemmed TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title_short TNF-α Predicts Endothelial Function and Number of CD34(+) Cells after Stimulation with G-CSF in Patients with Advanced Heart Failure
title_sort tnf-α predicts endothelial function and number of cd34(+) cells after stimulation with g-csf in patients with advanced heart failure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410381/
https://www.ncbi.nlm.nih.gov/pubmed/36005445
http://dx.doi.org/10.3390/jcdd9080281
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