Meta-analysis of the efficacy of granulocyte-colony stimulating factor in animal models of focal cerebral ischemia

被引:111
作者
Minnerup, Jens [1 ]
Heidrich, Jan [2 ]
Wellmann, Juergen [2 ]
Rogalewski, Andreas [1 ]
Schneider, Armin [3 ]
Schaebitz, Wolf-Ruediger [1 ]
机构
[1] Univ Munster, Dept Neurol, D-4400 Munster, Germany
[2] Univ Munster, Inst Epidemiol & Social Med, D-48149 Munster, Germany
[3] Sygnis Biosci, Heidelberg, Germany
关键词
stroke; hematopoietic cell growth factors; meta-analysis; animal models;
D O I
10.1161/STROKEAHA.107.506816
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Recent reports have described the efficacy of the hematopoietic growth factor granulocyte-colony stimulating factor (G-CSF) in animal stroke models. Early clinical multicenter trials evaluating the effect of G-CSF in acute stroke and pilot clinical trials for the subacute phase are ongoing. To guide further development, a meta-analysis was performed to assess the effects of G-CSF on infarct size and sensorimotor deficits. Methods-Using electronic and manual searches of the literature, we identified studies describing the efficacy of G-CSF in animal models of focal cerebral ischemia. Two reviewers independently selected studies and extracted data on study quality, G-CSF doses, time of administration, and outcome measured as infarct volume and/ or sensorimotor deficit. Data from all studies were pooled by meta-regression analyses. Results-Thirteen studies including 277 animals for infarct size calculation and 258 animals for assessment of sensorimotor deficit met the criteria for inclusion. Overall efficacy of G-CSF regarding infarct size reduction was 42%. Meta-regression analysis revealed a 0.8% (P<0.0001) decrease in infarct size per 1-mu g/kg increase in G-CSF dose when applied within the first 6 hours and a 2.1% (P<0.0001) decrease when applied later than 6 hours after induction of ischemia with a significant (P<0.0004) greater infarct size reduction after delayed treatment. Sensorimotor deficits categorized into 3 subgroups improved between 24% and 40%. Conclusions-Our findings consolidate G-CSF as a drug that both reduces infarct size and enhances functional recovery. These effects are presumably dose dependent. In contrast to most other neuroprotectants, a beneficial outcome may also be achieved when treatment is delayed.
引用
收藏
页码:1855 / 1861
页数:7
相关论文
共 41 条
[1]  
[Anonymous], 2001, SYSTEMATIC REV HLTH, DOI DOI 10.1002/9780470693926
[2]  
Bishop M.M., 1975, DISCRETE MULTIVARIAT
[3]   Three to six year follow-up of normal donors who received recombinant human granulocyte colony-stimulating factor [J].
Cavallaro, AM ;
Lilleby, K ;
Majolino, I ;
Storb, R ;
Appelbaum, FR ;
Rowley, SD ;
Bensinger, WI .
BONE MARROW TRANSPLANTATION, 2000, 25 (01) :85-89
[4]  
Chen Song-Lin, 2005, Di Yi Jun Yi Da Xue Xue Bao, V25, P503
[5]   Neuroprotection failure in stroke [J].
Drummond, JC ;
Piyash, PM ;
Kimbro, JR .
LANCET, 2000, 356 (9234) :1032-1033
[6]   Recommendations for standards regarding preclinical neuroprotective and restorative drug development [J].
Feinklestein, SP ;
Fisher, M ;
Furland, AJ ;
Goldstein, LB ;
Gorelick, PB ;
Kaste, M ;
Lees, KR ;
Traystman, RJ ;
Albers, GW ;
Anwer, UE ;
Ashwood, T ;
Barone, FC ;
Basta, SL ;
Bogousslavsky, J ;
Buchan, AM ;
Cady, WJ ;
Chan, PH ;
Clemens, JA ;
Cox, BF ;
Craddock, RE ;
Cramer, SC ;
del Zoppo, GJ ;
Dielrich, WD ;
Elliott, P ;
Faden, AI ;
Feuerstein, GZ ;
Ginsberg, MD ;
Gold, M ;
Greene, WL ;
Hall, ED ;
Hsu, CY ;
Hunter, AJ ;
Lai, M ;
Lesko, LM ;
Levy, DE ;
Li, FH ;
Locke, KW ;
Lodge, D ;
Lowe, D ;
Marcoux, FW ;
McCulloch, J ;
McDermott, J ;
Meibach, R ;
Messersmith, EK ;
Moseley, M ;
Moskowitz, MA ;
Mueller, AL ;
Munro, F ;
Nudo, RJ ;
Oeda, J .
STROKE, 1999, 30 (12) :2752-2758
[7]  
FIELLER EC, 1954, J ROY STAT SOC B, V16, P175
[8]   FILGRASTIM - A REVIEW OF ITS PHARMACOLOGICAL PROPERTIES AND THERAPEUTIC EFFICACY IN NEUTROPENIA [J].
FRAMPTON, JE ;
LEE, CR ;
FAULDS, D .
DRUGS, 1994, 48 (05) :731-760
[9]   G-CSF reduces infarct volume and improves functional outcome after transient focal cerebral ischemia in mice [J].
Gibson, CL ;
Bath, PMW ;
Murphy, SP .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2005, 25 (04) :431-439
[10]   G-CSF suppresses edema formation and reduces interleukin-1β expression after cerebral ischemia in mice [J].
Gibson, CL ;
Jones, NC ;
Prior, MJW ;
Bath, PMW ;
Murphy, SP .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2005, 64 (09) :763-769