Colony stimulating factors (including erythropoietin, granulocyte colony stimulating factor and analogues) for stroke

被引:4
作者
Bath, P. M. W. [1 ]
Sprigg, N. [1 ]
机构
[1] Univ Nottingham, Div Stroke Med, Queens Med Ctr, Nottingham NG7 2UH, England
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2006年 / 03期
关键词
D O I
10.1002/14651858.CD005207.pub2
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background Colony stimulating factors (CSFs), also called haematopoietic growth factors, regulate bone marrow production of circulating red and white cells, and platelets. They have been shown to be neuroprotective in experimental stroke. Some CSFs also mobilise the release of bone marrow stem cells into the circulation. Objectives We systematically assessed the effects of CSFs on functional outcome and haematology measures in patients with acute or subacute stroke enrolled into randomised controlled trials. Search strategy We searched the Cochrane Stroke Group Trials Register (last searched February 2005), the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 3, 2005), MEDLINE (1985 to March 2006), EMBASE (1985 to November 2005), and Science Citation Index (1985 to November 2005). In an attempt to identify further published, unpublished and ongoing trials we contacted manufacturers and principal investigators of trials (last contacted 2005). We also searched reference lists of relevant articles and reviews. Selection criteria Unconfounded randomised controlled trials recruiting patients with acute or subacute ischaemic or haemorrhagic stroke were included. CSFs included stem cell factor (SCF), erythropoietin (EPO), granulocyte colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), macrophage-colony stimulating factor (M-CSF, CSF-1), and thrombopoietin (TPO), or analogues of these. The primary outcome was functional outcome (assessed as combined death or disability and dependency using scales such as the modified Rankin Scale or Barthel Index) at the end of the trial. Secondary outcomes included safety at the end of treatment (death, impairment, deterioration, extension or recurrence), death at the end of follow up, and haematology measures (blood counts at or around day seven after treatment commenced). Data collection and analysis Data on measures by intention to treat (where available) were collected and analysed as dichotomous or continuous outcomes, as relevant, using random-effects models. Heterogeneity was assessed. Main results No large trials were identified. EPO therapy was associated with a non-significant reduction in neurological impairment in one small trial (n = 40 participants) but had no significant effect on haematological measures. Further small trials of EPO and G-CSF are ongoing. Authors' conclusions No large trials of EPO, G-CSF or other colony stimulating factors have been performed and it is too early to know whether CSFs improve functional outcome.
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页数:15
相关论文
共 27 条
[1]
BATH PMW, 2004, ISRCTN REGISTER
[2]
Colony stimulating factor-1 potentiates neuronal survival in cerebral cortex ischemic lesion [J].
Berezovskaya, O ;
Maysinger, D ;
Fedoroff, S .
ACTA NEUROPATHOLOGICA, 1996, 92 (05) :479-486
[3]
BOGDAHN U, 2005, COMMUNICATION
[4]
Erythropoietin crosses the blood-brain barrier to protect against experimental brain injury [J].
Brines, ML ;
Ghezzi, P ;
Keenan, S ;
Agnello, D ;
de Lanerolle, NC ;
Cerami, C ;
Itri, LM ;
Cerami, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10526-10531
[5]
Therapeutic induction of arteriogenesis in hypoperfused rat brain via granulocyte-macrophage colony-stimulating factor [J].
Buschmann, IR ;
Busch, HJ ;
Mies, G ;
Hossmann, KA .
CIRCULATION, 2003, 108 (05) :610-615
[6]
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatment [J].
Corti, S ;
Locatelli, F ;
Strazzer, S ;
Salani, S ;
Del Bo, R ;
Soligo, D ;
Bossolasco, P ;
Bresolin, N ;
Scarlato, G ;
Comi, GP .
EXPERIMENTAL NEUROLOGY, 2002, 177 (02) :443-452
[7]
Erythropoietin therapy for acute stroke is both safe and beneficial [J].
Ehrenreich, H ;
Hasselblatt, M ;
Dembowski, C ;
Cepek, L ;
Lewczuk, P ;
Stiefel, M ;
Rustenbeck, HH ;
Breiter, N ;
Jacob, S ;
Knerlich, F ;
Bohn, M ;
Poser, W ;
Rüther, E ;
Kochen, M ;
Gefeller, O ;
Gleiter, C ;
Wessel, TC ;
De Ryck, M ;
Itri, L ;
Prange, H ;
Cerami, A ;
Brines, M ;
Sirén, AL .
MOLECULAR MEDICINE, 2002, 8 (08) :495-505
[8]
Asialoerythropoietin is a nonerythropoietic cytokine with broad neuroprotective activity in vivo [J].
Erbayraktar, S ;
Grasso, G ;
Sfacteria, A ;
Xie, QW ;
Coleman, T ;
Kreilgaard, M ;
Torup, L ;
Sager, T ;
Erbayraktar, Z ;
Gokmen, N ;
Yilmaz, O ;
Ghezzi, P ;
Villa, P ;
Fratelli, M ;
Casagrande, S ;
Leist, M ;
Helboe, L ;
Gerwein, J ;
Christensen, S ;
Geist, MA ;
Pedersen, LO ;
Cerami-Hand, C ;
Wuerth, JP ;
Cerami, A ;
Brines, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6741-6746
[9]
GABRILOVE JL, 1994, BLOOD, V83, P907
[10]
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