1 Department of Paediatric Neurology, Queensland Cerebral Palsy and Rehabilitation Research, Child Health Research Centre, Faculty of Medicine, The University of Queensland , Queensland, Australia .
2 Department of Paediatric Neurology, Neurocritical Care Program, Alberta Children's Hospital Research Institute, University of Calgary , Calgary, Alberta, Canada .
J Neurotrauma. 2019 Feb 15;36(4):523-537. doi: 10.1089/neu.2018.5752. Epub 2018 Sep 4.
Traumatic brain injury (TBI) is common; however, effective treatments of the secondary brain injury are scarce. Melatonin is a potent, nonselective neuroprotective and anti-inflammatory agent that is showing promising results in neonatal brain injury. The aim of this study was to systematically evaluate the pre-clinical and clinical literature on the effectiveness of melatonin in improving outcome after TBI. Using the systematic review protocol for animal intervention studies (SYRCLE) and Cochrane methodology for clinical studies, a search of English-language articles was performed. Eligible studies were identified and data were extracted. Quality assessment was performed using the SYRCLE risk of bias tool. Meta-analyses were performed using standardized mean differences (SMD). Seventeen studies (15 pre-clinical, 2 clinical) met inclusion criteria. There was heterogeneity in the studies, and all had moderate-to-low risk of bias. Meta-analysis of pre-clinical data revealed an overall positive effect on neurobehavioural outcome with SMD of 1.51 (95% CI: 1.06-1.96). Melatonin treatment had a favorable effect on neurological status, by an SMD of 1.35 (95% CI: 0.83-1.88), and on cognition by an SMD of 1.16 (95% CI: 0.4-1.92). Melatonin decreased the size of the contusion by an SMD of 2.22 (95% CI: 0.8--3.59) and of cerebral edema by an SMD of 1.91 (95% CI: 1.08-2.74). Only two clinical studies were identified. They were of low quality, were used for symptom management, and were of uncertain significance. In conclusion, there is evidence that melatonin treatment after TBI significantly improves both behavioral outcomes and pathological outcomes; however, significant research gaps exist, especially in clinical populations.
创伤性脑损伤(TBI)很常见;然而,有效的二次脑损伤治疗方法却很少。褪黑素是一种有效的、非选择性的神经保护和抗炎药物,在新生儿脑损伤中显示出有希望的结果。本研究旨在系统评价褪黑素在改善 TBI 后结局的临床前和临床文献。使用动物干预研究的系统评价协议(SYRCLE)和临床研究的 Cochrane 方法,对英文文章进行了搜索。确定了合格的研究并提取了数据。使用 SYRCLE 偏倚风险工具进行了质量评估。使用标准化均数差(SMD)进行了荟萃分析。17 项研究(15 项临床前,2 项临床)符合纳入标准。研究存在异质性,所有研究的偏倚风险均为中低。临床前数据分析显示,神经行为结局的总体效果为正,SMD 为 1.51(95%CI:1.06-1.96)。褪黑素治疗对神经状态有有利影响,SMD 为 1.35(95%CI:0.83-1.88),对认知功能有有利影响,SMD 为 1.16(95%CI:0.4-1.92)。褪黑素使挫伤体积缩小 SMD 为 2.22(95%CI:0.8-3.59),脑水肿缩小 SMD 为 1.91(95%CI:1.08-2.74)。仅确定了两项临床研究。它们的质量较低,用于症状管理,意义不确定。总之,有证据表明 TBI 后褪黑素治疗可显著改善行为结局和病理结局;然而,仍存在显著的研究空白,尤其是在临床人群中。