Melatonin as a Treatment after Traumatic Brain Injury: A Systematic Review and Meta-Analysis of the Pre-Clinical and Clinical Literature.


Journal

Journal of neurotrauma
ISSN: 1557-9042
Titre abrégé: J Neurotrauma
Pays: United States
ID NLM: 8811626

Informations de publication

Date de publication:
15 02 2019
Historique:
pubmed: 15 6 2018
medline: 14 7 2020
entrez: 15 6 2018
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 29901413
doi: 10.1089/neu.2018.5752
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Neuroprotective Agents 0
Melatonin JL5DK93RCL

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

523-537

Auteurs

Karen M Barlow (KM)

1 Department of Paediatric Neurology, Queensland Cerebral Palsy and Rehabilitation Research, Child Health Research Centre, Faculty of Medicine, The University of Queensland , Queensland, Australia .

Michael J Esser (MJ)

2 Department of Paediatric Neurology, Neurocritical Care Program, Alberta Children's Hospital Research Institute, University of Calgary , Calgary, Alberta, Canada .

Myra Veidt (M)

2 Department of Paediatric Neurology, Neurocritical Care Program, Alberta Children's Hospital Research Institute, University of Calgary , Calgary, Alberta, Canada .

Roslyn Boyd (R)

3 Department of Cerebral Palsy and Rehabilitation Research, Queensland Cerebral Palsy and Rehabilitation Research, Child Health Research Centre, Faculty of Medicine, The University of Queensland , Queensland, Australia .

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Classifications MeSH