Fan Zhen-Zhen, Cai Hong-Bin, Ge Zhao-Ming, Wang Li-Qun, Zhang Xu-Dong, Li Ling, Zhai Xiao-Bin
Department of Neurology, Second Hospital of Lanzhou University, Lanzhou, China.
Department of Neurology, Second Hospital of Lanzhou University, Lanzhou, China.
J Stroke Cerebrovasc Dis. 2015 Aug;24(8):1701-8. doi: 10.1016/j.jstrokecerebrovasdis.2014.11.033. Epub 2015 May 23.
Granulocyte colony-stimulating factor (G-CSF) has been shown to reduce lesion volume and improve functional outcome in experimental stroke models. However, whether G-CSF plays a role currently in patients with stroke remains uncertain. Our study aimed at examining the efficacy and safety of G-CSF in patients with acute ischemic stroke.
A comprehensive search was conducted in 5 online databases up to April 2014, and 10 studies with 711 patients met the criteria.
The results showed that G-CSF was beneficial in improving the National Institutes of Health Stroke Scale (standardized mean difference [SMD], .43; 95% confidence interval [CI], .03-.82; P = .04) and modified Rankin Scale (mRS) scores (SMD, .72; 95% CI, .51-.93; P = .01), and elevating CD34(+) count (P < .001). No treatment effects were found in Barthel Index scores (SMD, -.13; 95% CI, -.61 to .35; P = .59), serious adverse events (relative ratio [RR], 1.12; 95% CI, .91-1.38; P = .28), or the death of serious adverse events (RR, 1.25; 95% CI, .82-1.91; P = .30) between groups at day 90. Adverse effect on vascular complications was not detected to be increased although G-CSF produced a marked elevation in the total leukocyte count (SMD, 3.52; 95% CI, 2.54-4.49; P < .001).
In conclusion, G-CSF is effective at mobilizing bone marrow-derived CD34(+) stem cells to the peripheral blood. It also seems to improve the National Institutes of Health Stroke Scale and mRS scores. The administration of G-CSF appears to be safe and well tolerated. Further studies need to be done on a large sample to verify or fully characterize the results.
在实验性卒中模型中,粒细胞集落刺激因子(G-CSF)已被证明可减少损伤体积并改善功能结局。然而,G-CSF目前在卒中患者中是否起作用仍不确定。我们的研究旨在检验G-CSF对急性缺血性卒中患者的疗效和安全性。
截至2014年4月,在5个在线数据库中进行了全面检索,10项研究共711例患者符合标准。
结果显示,G-CSF有助于改善美国国立卫生研究院卒中量表(标准化均数差[SMD],0.43;95%置信区间[CI],0.03 - 0.82;P = 0.04)和改良Rankin量表(mRS)评分(SMD,0.72;95% CI,0.51 - 0.93;P = 0.01),并提高CD34(+)计数(P < 0.001)。在第90天时,两组间Barthel指数评分(SMD,-0.13;95% CI,-0.61至0.35;P = 0.59)、严重不良事件(相对比[RR],1.12;95% CI,0.91 - 1.38;P = 0.28)或严重不良事件导致的死亡(RR,1.25;95% CI,0.82 - 1.91;P = 0.30)方面未发现治疗效果。尽管G-CSF使总白细胞计数显著升高(SMD,3.52;95% CI,2.54 - 4.49;P < 0.001),但未检测到对血管并发症的不良影响增加。
总之,G-CSF可有效动员骨髓源性CD34(+)干细胞至外周血。它似乎还能改善美国国立卫生研究院卒中量表和mRS评分。G-CSF的给药似乎是安全且耐受性良好的。需要进行更大样本的进一步研究以验证或充分描述这些结果。