Bone marrow mobilization with granulocyte macrophage colony-stimulating factor improves endothelial dysfunction and exercise capacity in patients with peripheral arterial disease
We hypothesized that granulocyte macrophage colony-stimulating factor (GM-CSF) administration will be safe and will improve endothelial dysfunction and exercise capacity by mobilizing progenitor cells in patients with peripheral arterial disease (PAD). Forty-five patients with PAD received thrice-we...
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Published in | The American heart journal Vol. 158; no. 1; pp. 53 - 60.e1 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Mosby, Inc
01.07.2009
Mosby Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0002-8703 1097-6744 1097-6744 |
DOI | 10.1016/j.ahj.2009.04.014 |
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Summary: | We hypothesized that granulocyte macrophage colony-stimulating factor (GM-CSF) administration will be safe and will improve endothelial dysfunction and exercise capacity by mobilizing progenitor cells in patients with peripheral arterial disease (PAD).
Forty-five patients with PAD received thrice-weekly injections for 2 weeks of 3, 6, or 10 μg/kg per day of GM-CSF or placebo in successive cohorts of 15 subjects randomized 2:1 to drug or placebo. CD34
+ mononuclear cell subsets and colony formation assay, endothelial function, ankle-brachial index, and walking capacity were measured.
Granulocyte macrophage colony-stimulating factor administration was safe. After pooling data from GM-CSF cohorts, at 2 weeks, there was a significant increase in total leukocytes (43%,
P < .0001), CD34
+ cells (46%,
P = .035), and colony-forming units (31%,
P = .026, week 1). At 12 weeks, endothelial function improved with GM-CSF (flow-mediated vasodilation increased by 59%,
P < .01) as did pain-free treadmill walking time (38 seconds,
P = .008) and total treadmill walking time (55 seconds,
P = .016). Corresponding changes were not observed in the placebo group.
Granulocyte macrophage colony-stimulating factor therapy in patients with PAD was associated with mobilization of progenitor cells, improvement of endothelial dysfunction, and exercise capacity. The efficacy of strategies designed to mobilize bone marrow progenitors warrants further study in patients with PAD. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 |
ISSN: | 0002-8703 1097-6744 1097-6744 |
DOI: | 10.1016/j.ahj.2009.04.014 |