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Niels van Royen(University of Freiburg), Stephan H. Schirmer(University of Freiburg), Bektaş Atasever(University of Freiburg), Casper Y.H. Behrens(University of Freiburg), Dirk T. Ubbink(University of Freiburg), Eva Buschmann(University of Freiburg), Michiel Voskuil(University of Freiburg), Pieter T. Bot(University of Freiburg), Imo E. Hoefer(University of Freiburg), Reinier O. Schlingemann(University of Freiburg), Bart J. Biemond(Max Planck Institute for Heart and Lung Research), Jan G.P. Tijssen(University of Freiburg), Christoph Bode(University of Freiburg), Wolfgang Schäper(University of Freiburg), J. Oskam(University of Freiburg), D.A. Legemate(University of Freiburg), Jan J. Piek(University of Freiburg), Ivo Buschmann(University of Freiburg)
Circulation
August 9, 2005
Cited by 143Open Access
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Abstract

BACKGROUND: Granulocyte-macrophage colony-stimulating factor (GM-CSF) was recently shown to increase collateral flow index in patients with coronary artery disease. Experimental models showed beneficial effects of GM-CSF on collateral artery growth in the peripheral circulation. Thus, in the present study, we evaluated the effects of GM-CSF in patients with peripheral artery disease. METHODS AND RESULTS: A double-blinded, randomized, placebo-controlled study was performed in 40 patients with moderate or severe intermittent claudication. Patients were treated with placebo or subcutaneously applied GM-CSF (10 microg/kg) for a period of 14 days (total of 7 injections). GM-CSF treatment led to a strong increase in total white blood cell count and C-reactive protein. Monocyte fraction initially increased but thereafter decreased significantly as compared with baseline. Both the placebo group and the treatment group showed a significant increase in walking distance at day 14 (placebo: 127+/-67 versus 184+/-87 meters, P=0.03, GM-CSF: 126+/-66 versus 189+/-141 meters, P=0.04) and at day 90. Change in walking time, the primary end point of the study, was not different between groups. No change in ankle-brachial index was found on GM-CSF treatment at day 14 or at day 90. Laser Doppler flowmetry measurements showed a significant decrease in microcirculatory flow reserve in the control group (P=0.03) and no change in the GM-CSF group. CONCLUSIONS: The present study does not support the use of GM-CSF for treatment of patients with moderate or severe intermittent claudication. Issues that need to be addressed are dosing, the selection of patients, and potential differences between GM-CSF effects in the coronary and the peripheral circulation.


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