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首页> 外文期刊>Frontiers in Neurology >Efficacy and the Safety of Granulocyte Colony-Stimulating Factor Treatment in Patients with Muscular Dystrophy: A Non-Randomized Clinical Trial
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Efficacy and the Safety of Granulocyte Colony-Stimulating Factor Treatment in Patients with Muscular Dystrophy: A Non-Randomized Clinical Trial

机译:肌营养不良患者的粒细胞集落刺激因子治疗的疗效和安全性:一项非随机临床试验

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Introduction The current standard treatment for patients with Duchenne muscular dystrophy (DMD) involves corticosteroids. Granulocyte colony-stimulating factor (G-CSF) induces the proliferation of satellite cells and myoblasts and, in turn, muscle regeneration. Beneficial effects of G-CSF were also described for skeletal muscle disorders. Aim We assessed the safety and effects of using G-CSF to promote muscle strength in patients with DMD. Materials and methods Inclusion criteria were as follows: patients aged 5–15?years with diagnosed with DMD confirmed by genetic test or biopsy. Fourteen patients were treated with steroids, and their use was not changed in this study. Diagnoses were confirmed by genetic tests: deletions were detected in 11 patients and duplications in 5 patients. Nineteen 5- to 15-year-old patients diagnosed with DMD—9 were in wheelchairs, whereas 10 were mobile and independent—completed an open study. Participants received a clinical examination and performed physiotherapeutic and laboratory tests to gage their manual muscle strength, their isometric force using a hand dynamometer, and aerobic capacity [i.e., 6-min walk test (6MWT)] before and after therapy. Each participant received G-CSF (5?μg/kg/body/day) subcutaneously for five consecutive days during the 1st, 2nd, 3rd, 6th, and 12th month. Laboratory investigations that included full blood count and biochemistry were performed. Side effects of G-CSF treatment were assessed during each visit. During each cycle of G-CSF administration in the hospital, rehabilitation was also applied. All patients received regular ambulatory rehabilitation. Results The subcutaneous administration of G-CSF improved muscle strength in participants. We recorded a significant increase in the distance covered in the 6MWT, either on foot or in a wheelchair, increased muscle force in isometric force, and a statistically significant decrease in the activity of the muscle enzyme creatine kinase after nearly every cycle of treatment. We observed no side effects of treatment with G-CSF. Conclusion Our findings suggest that G-CSF increases muscle strength in patients with DMD, who demonstrated that G-CSF therapy is safe and easily tolerable.
机译:简介当前对杜氏肌营养不良症(DMD)患者的标准治疗方法包括皮质类固醇激素。粒细胞集落刺激因子(G-CSF)诱导卫星细胞和成肌细胞增殖,进而引起肌肉再生。还描述了G-CSF对骨骼肌疾病的有益作用。目的我们评估了使用G-CSF增强DMD患者肌肉力量的安全性和效果。材料和方法纳入标准如下:5-15岁的经遗传学检查或活检确诊为DMD的患者。接受类固醇治疗的患者为14名,其使用在本研究中未发生变化。通过基因检测证实了诊断:11例患者发现缺失,5例患者发现重复。 19名诊断为DMD的5至15岁患者中有9人坐在轮椅上,而10人是可移动且独立的,他们完成了一项开放研究。参与者接受了临床检查,并在治疗前后进行了理疗和实验室测试,以衡量其手动肌肉力量,使用测功机的等距力量以及有氧能力[即6分钟步行测试(6MWT)]。在第一,第二,第三,第六和第十二个月,每位参与者连续五天皮下接受G-CSF(5?g / kg /体/天)。进行了包括全血细胞计数和生物化学在内的实验室检查。每次访视期间评估G-CSF治疗的副作用。在医院进行G-CSF行政管理的每个周期中,还进行了康复治疗。所有患者均接受定期门诊康复治疗。结果皮下注射G-CSF可改善参与者的肌肉强度。我们记录了在6MWT中行走或坐在轮椅上的距离显着增加,等轴测力中的肌肉力量增加,并且在几乎每个治疗周期后,肌肉酶肌酸激酶的活性均在统计学上显着降低。我们没有观察到用G-CSF治疗的副作用。结论我们的发现表明,G-CSF可以增加DMD患者的肌肉力量,这表明G-CSF治疗是安全且容易耐受的。

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