实验性脊髓损伤后靶向神经纤维生长抑制:软骨素酶ABC的系统回顾和荟萃分析。

Alireza Khanteymoori, Clayton Peterson, Roza Atamny, Marc Hohenhaus, Jürgen Beck, David W Howells, Jan M Schwab, Ralf Watzlawick
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引用次数: 0

摘要

背景:脊髓损伤(SCI)可损害运动、感觉和自主神经功能。胶质瘢痕的形成包括保护和抑制神经突生长的特性,由硫酸软骨素蛋白聚糖(CSPG)的沉积操作。软骨素酶ABC (ChABC)可以降解CSPG并促进神经轴突可塑性,作为恢复脊髓损伤后运动功能的治疗方法。目的:为了系统地回顾脊髓损伤后的ChABC治疗实验并评估其对运动功能的疗效,根据预注册的普洛斯普洛研究方案进行了全面的文献检索,选择了评估创伤性脊髓损伤后神经行为结果的动物研究,然后使用荟萃分析和荟萃回归方法计算归一化效应量。进一步分析动物类型、品系、性别、样本量、损伤模型、损伤程度和治疗时间的影响。结果:在1066只动物的整体分析中,观察到相当多的异质性。亚组分析包括采用相同神经行为测量(血脑屏障/ basso -小鼠量表[BMS]-亚组)的实验,结果显示运动结果改善15.9% (95% CI = 11.3%-20.6%)。不同的实验特征影响神经恢复,包括性别、损伤程度、使用的麻醉剂、报告的ChABC治疗剂量、评估时间点和围手术期体温控制。应用Trim和Fill进行敏感性分析,确定了19个假设缺失的实验,提示报告偏差。结论:SCI实验研究的报告偏倚是普遍存在的,并不局限于特定的干预措施。ChABC治疗对脊髓损伤后的运动恢复有有益的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting Nerve Fiber Outgrowth Inhibition After Experimental Spinal Cord Injury: A Systematic Review and Meta-analysis of Chondroitinase ABC.

Background: Spinal cord injury (SCI) can impair motor, sensory, and autonomic function. The formation of the glial scar comprises protective as well as inhibitory neurite outgrowth properties operated by the deposition of chondroitin sulfate proteoglycans (CSPG). Chondroitinase ABC (ChABC) can degrade CSPG and foster neuroaxonal plasticity as a therapeutic approach to restore locomotor function after SCI.

Objectives: To systematically review experimental ChABC treatments after SCI and assess their efficacy for locomotor function a comprehensive literature search was conducted following pre-registered Prospero Study protocol, selecting animal studies evaluating neurobehavioral outcomes after traumatic SCI followed by the calculation of normalized effect sizes applying meta-analysis and meta-regression methodology. Additional analyses were performed to investigate the impact of animal type, strain, sex, sample size, injury models, level of injury, and treatment duration.

Results: Within the overall analysis of 1066 animals, a considerable amount of heterogeneity was observed. A subgroup analysis comprising experiments applying the same neurobehavioral measurement (blood-brain barrier/Basso-Mouse-Scale [BMS]-subgroup) demonstrated a 15.9% (95% CI = 11.3%-20.6%) improvement in locomotor outcomes. Different experimental characteristics influenced neurological recovery, including sex, level of injury, used anesthetic, reported dosage of ChABC treatment, the timepoint of assessment and perioperative temperature control. Sensitivity analysis applying Trim and Fill identified 19 hypothetical missing experiments suggestive of reporting bias.

Conclusion: Reporting bias in experimental SCI research is prevalent and not limited to a specific intervention. ChABC treatment can exert beneficial effects on locomotor recovery after SCI.

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