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Bone marrow mobilization with granulocyte macrophage colony-stimulating factor improves endothelial dysfunction and exercise capacity in patients with peripheral arterial disease
Background 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). Methods Forty-five patients with PAD...
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Published in: | The American heart journal 2009-07, Vol.158 (1), p.53-60.e1 |
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creator | Subramaniyam, Veerappan, MD Waller, Edmund K., MD, PhD Murrow, Jonathan R., MD Manatunga, Amita, PhD Lonial, Sagar, MD Kasirajan, Karthikeswar, MD Sutcliffe, Diane, BS Harris, Wayne, BS Taylor, W. Robert, MD, PhD, FACC Alexander, R. Wayne, MD, PhD, FACC Quyyumi, Arshed A., MD, FACC |
description | Background 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). Methods 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. Results 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. Conclusions 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. |
doi_str_mv | 10.1016/j.ahj.2009.04.014 |
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Robert, MD, PhD, FACC ; Alexander, R. Wayne, MD, PhD, FACC ; Quyyumi, Arshed A., MD, FACC</creator><creatorcontrib>Subramaniyam, Veerappan, MD ; Waller, Edmund K., MD, PhD ; Murrow, Jonathan R., MD ; Manatunga, Amita, PhD ; Lonial, Sagar, MD ; Kasirajan, Karthikeswar, MD ; Sutcliffe, Diane, BS ; Harris, Wayne, BS ; Taylor, W. Robert, MD, PhD, FACC ; Alexander, R. Wayne, MD, PhD, FACC ; Quyyumi, Arshed A., MD, FACC</creatorcontrib><description>Background 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). Methods 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. Results 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. Conclusions 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.</description><identifier>ISSN: 0002-8703</identifier><identifier>EISSN: 1097-6744</identifier><identifier>DOI: 10.1016/j.ahj.2009.04.014</identifier><identifier>PMID: 19540392</identifier><identifier>CODEN: AHJOA2</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Acute coronary syndromes ; Aged ; Ankle Brachial Index ; Arterial Occlusive Diseases - drug therapy ; Atherosclerosis - drug therapy ; Biological and medical sciences ; Blood and lymphatic vessels ; Bone marrow ; Bone Marrow - drug effects ; Cardiology. Vascular system ; Cardiovascular ; Colonies & territories ; Colony-Forming Units Assay ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Dose-Response Relationship, Drug ; Double-Blind Method ; Drug Administration Schedule ; Endothelium ; Endothelium, Vascular - drug effects ; Endothelium, Vascular - physiopathology ; Exercise Test - drug effects ; Female ; Flow Cytometry ; Granulocyte-Macrophage Colony-Stimulating Factor - administration & dosage ; Granulocyte-Macrophage Colony-Stimulating Factor - adverse effects ; Hematopoietic Stem Cell Mobilization - methods ; Humans ; Leukocyte Count ; Male ; Medical sciences ; Middle Aged ; Vascular endothelial growth factor ; Vasodilation ; Walking</subject><ispartof>The American heart journal, 2009-07, Vol.158 (1), p.53-60.e1</ispartof><rights>Mosby, Inc.</rights><rights>2009 Mosby, Inc.</rights><rights>2009 INIST-CNRS</rights><rights>Copyright Elsevier Limited Jul 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-7195c264ba280c404ae29558662ed24cf0ee92ae475018e59609b3d7f1c133843</citedby><cites>FETCH-LOGICAL-c464t-7195c264ba280c404ae29558662ed24cf0ee92ae475018e59609b3d7f1c133843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21699113$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19540392$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Subramaniyam, Veerappan, MD</creatorcontrib><creatorcontrib>Waller, Edmund K., MD, PhD</creatorcontrib><creatorcontrib>Murrow, Jonathan R., MD</creatorcontrib><creatorcontrib>Manatunga, Amita, PhD</creatorcontrib><creatorcontrib>Lonial, Sagar, MD</creatorcontrib><creatorcontrib>Kasirajan, Karthikeswar, MD</creatorcontrib><creatorcontrib>Sutcliffe, Diane, BS</creatorcontrib><creatorcontrib>Harris, Wayne, BS</creatorcontrib><creatorcontrib>Taylor, W. Robert, MD, PhD, FACC</creatorcontrib><creatorcontrib>Alexander, R. Wayne, MD, PhD, FACC</creatorcontrib><creatorcontrib>Quyyumi, Arshed A., MD, FACC</creatorcontrib><title>Bone marrow mobilization with granulocyte macrophage colony-stimulating factor improves endothelial dysfunction and exercise capacity in patients with peripheral arterial disease</title><title>The American heart journal</title><addtitle>Am Heart J</addtitle><description>Background 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). Methods 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. Results 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. Conclusions 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.</description><subject>Acute coronary syndromes</subject><subject>Aged</subject><subject>Ankle Brachial Index</subject><subject>Arterial Occlusive Diseases - drug therapy</subject><subject>Atherosclerosis - drug therapy</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Bone marrow</subject><subject>Bone Marrow - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Colonies & territories</subject><subject>Colony-Forming Units Assay</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. 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Wayne, MD, PhD, FACC</creatorcontrib><creatorcontrib>Quyyumi, Arshed A., MD, FACC</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Health Management</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>The American heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subramaniyam, Veerappan, MD</au><au>Waller, Edmund K., MD, PhD</au><au>Murrow, Jonathan R., MD</au><au>Manatunga, Amita, PhD</au><au>Lonial, Sagar, MD</au><au>Kasirajan, Karthikeswar, MD</au><au>Sutcliffe, Diane, BS</au><au>Harris, Wayne, BS</au><au>Taylor, W. Robert, MD, PhD, FACC</au><au>Alexander, R. Wayne, MD, PhD, FACC</au><au>Quyyumi, Arshed A., MD, FACC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone marrow mobilization with granulocyte macrophage colony-stimulating factor improves endothelial dysfunction and exercise capacity in patients with peripheral arterial disease</atitle><jtitle>The American heart journal</jtitle><addtitle>Am Heart J</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>158</volume><issue>1</issue><spage>53</spage><epage>60.e1</epage><pages>53-60.e1</pages><issn>0002-8703</issn><eissn>1097-6744</eissn><coden>AHJOA2</coden><abstract>Background 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). Methods 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. Results 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. Conclusions 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.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>19540392</pmid><doi>10.1016/j.ahj.2009.04.014</doi><tpages>8</tpages></addata></record> |
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subjects | Acute coronary syndromes Aged Ankle Brachial Index Arterial Occlusive Diseases - drug therapy Atherosclerosis - drug therapy Biological and medical sciences Blood and lymphatic vessels Bone marrow Bone Marrow - drug effects Cardiology. Vascular system Cardiovascular Colonies & territories Colony-Forming Units Assay Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Dose-Response Relationship, Drug Double-Blind Method Drug Administration Schedule Endothelium Endothelium, Vascular - drug effects Endothelium, Vascular - physiopathology Exercise Test - drug effects Female Flow Cytometry Granulocyte-Macrophage Colony-Stimulating Factor - administration & dosage Granulocyte-Macrophage Colony-Stimulating Factor - adverse effects Hematopoietic Stem Cell Mobilization - methods Humans Leukocyte Count Male Medical sciences Middle Aged Vascular endothelial growth factor Vasodilation Walking |
title | Bone marrow mobilization with granulocyte macrophage colony-stimulating factor improves endothelial dysfunction and exercise capacity in patients with peripheral arterial disease |
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