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Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization

INTRODUCTION: Prior in vivo murine studies suggest circadian oscillations for hematopoietic stem cell release, which are maintained following administration of granulocyte colony-stimulating factor (G-CSF) or plerixafor. Furthermore, retrospective data analysis of healthy donors who underwent G-CSF-...

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Autores principales: Shi, Patricia A, Isola, Luis M, Gabrilove, Janice L, Moshier, Erin L, Godbold, James H, Miller, Lorraine K, Frenette, Paul S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706980/
https://www.ncbi.nlm.nih.gov/pubmed/23514984
http://dx.doi.org/10.1186/scrt180
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author Shi, Patricia A
Isola, Luis M
Gabrilove, Janice L
Moshier, Erin L
Godbold, James H
Miller, Lorraine K
Frenette, Paul S
author_facet Shi, Patricia A
Isola, Luis M
Gabrilove, Janice L
Moshier, Erin L
Godbold, James H
Miller, Lorraine K
Frenette, Paul S
author_sort Shi, Patricia A
collection PubMed
description INTRODUCTION: Prior in vivo murine studies suggest circadian oscillations for hematopoietic stem cell release, which are maintained following administration of granulocyte colony-stimulating factor (G-CSF) or plerixafor. Furthermore, retrospective data analysis of healthy donors who underwent G-CSF-induced mobilization demonstrated significantly increased CD34(+) cell yields when collected in the afternoon compared with the morning. METHODS: A prospective study was conducted to directly examine the number of peripheral blood CD34(+) and CD34(+)CD38(–) progenitor/stem cells at baseline and then every 6 hours for 24 hours on days 4 to 5 of G-CSF (10 μg/kg/day in the morning) mobilization in 11 allogeneic donors. Data were analyzed using mixed-model analysis of repeated measures. RESULTS: Whereas we observed a significant increase in CD34(+) cell counts toward the evening, counts were then sustained on the morning of day 5. The correlation between CD34(+)CD38(–) cell counts and the less defined CD34(+) populations was weak. CONCLUSIONS: Our results suggest that the pharmacodynamic activity and timing of G-CSF may alter endogenous progenitor rhythms. Donor age, medical history, and medications may also impact circadian rhythm. Further studies should examine the circadian rhythm at the peak of G-CSF mobilization and should consider potential confounders such as the time of G-CSF administration and the age of the subjects.
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spelling pubmed-37069802013-07-15 Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization Shi, Patricia A Isola, Luis M Gabrilove, Janice L Moshier, Erin L Godbold, James H Miller, Lorraine K Frenette, Paul S Stem Cell Res Ther Research INTRODUCTION: Prior in vivo murine studies suggest circadian oscillations for hematopoietic stem cell release, which are maintained following administration of granulocyte colony-stimulating factor (G-CSF) or plerixafor. Furthermore, retrospective data analysis of healthy donors who underwent G-CSF-induced mobilization demonstrated significantly increased CD34(+) cell yields when collected in the afternoon compared with the morning. METHODS: A prospective study was conducted to directly examine the number of peripheral blood CD34(+) and CD34(+)CD38(–) progenitor/stem cells at baseline and then every 6 hours for 24 hours on days 4 to 5 of G-CSF (10 μg/kg/day in the morning) mobilization in 11 allogeneic donors. Data were analyzed using mixed-model analysis of repeated measures. RESULTS: Whereas we observed a significant increase in CD34(+) cell counts toward the evening, counts were then sustained on the morning of day 5. The correlation between CD34(+)CD38(–) cell counts and the less defined CD34(+) populations was weak. CONCLUSIONS: Our results suggest that the pharmacodynamic activity and timing of G-CSF may alter endogenous progenitor rhythms. Donor age, medical history, and medications may also impact circadian rhythm. Further studies should examine the circadian rhythm at the peak of G-CSF mobilization and should consider potential confounders such as the time of G-CSF administration and the age of the subjects. BioMed Central 2013-03-20 /pmc/articles/PMC3706980/ /pubmed/23514984 http://dx.doi.org/10.1186/scrt180 Text en Copyright © 2013 Shi 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
Shi, Patricia A
Isola, Luis M
Gabrilove, Janice L
Moshier, Erin L
Godbold, James H
Miller, Lorraine K
Frenette, Paul S
Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title_full Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title_fullStr Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title_full_unstemmed Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title_short Prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
title_sort prospective cohort study of the circadian rhythm pattern in allogeneic sibling donors undergoing standard granulocyte colony-stimulating factor mobilization
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706980/
https://www.ncbi.nlm.nih.gov/pubmed/23514984
http://dx.doi.org/10.1186/scrt180
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