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  4. Promising neuroprotective strategies for traumatic spinal cord injury with a focus on the differential effects among anatomical levels of injury

Promising neuroprotective strategies for traumatic spinal cord injury with a focus on the differential effects among anatomical levels of injury

F1000Research, 2017 · DOI: 10.12688/f1000research.11633.1 · Published: October 30, 2017

Spinal Cord InjuryNeurologyResearch Methodology & Design

Simple Explanation

Traumatic spinal cord injury (SCI) is a devastating condition of motor, sensory, and autonomic dysfunction. The significant cost associated with the management and lifetime care of patients with SCI also presents a major economic burden. This review highlights the most promising neuroprotective and neural reparative therapeutic strategies undergoing clinical assessment, including riluzole, hypothermia, granulocyte colony-stimulating factor, glibenclamide, minocycline, Cethrin (VX-210), and anti-Nogo-A antibody, and emphasizes their efficacy in relation to the anatomical level of injury. Our hope is that more basic research will be conducted in clinically relevant cervical SCI models in order to expedite the transition of important laboratory discoveries into meaningful treatment options for patients with SCI.

Study Duration
Not specified
Participants
Patients with traumatic spinal cord injury
Evidence Level
Review article

Key Findings

  • 1
    Early surgical decompression, which aims to realign the spinal column and relieve bony or ligamentous spinal cord compression, has preclinical and clinical success.
  • 2
    Riluzole, which inhibits voltage-gated sodium channels and glutamate release, thereby mitigating excitotoxicity, has shown statistically significant improvement compared with the control group in a phase I/IIA clinical trial.
  • 3
    Glibenclamide, by blocking NCCa-ATP channels, observed decreased lesion volumes and significant white matter preservation coupled with improved neurobehavioral outcomes.

Research Summary

This review highlights the most promising neuroprotective and neural reparative therapeutic strategies undergoing clinical assessment, including riluzole, hypothermia, granulocyte colony-stimulating factor, glibenclamide, minocycline, Cethrin (VX-210), and anti-Nogo-A antibody, and emphasizes their efficacy in relation to the anatomical level of injury. Spinal cord level-dependent differences in vertebral structure, anatomy, and peripheral immune organ innervation may affect SCI pathophysiology. Optimal patient recovery will stem from a combinatorial treatment regimen of integrated pharmacological and rehabilitation-based strategies that will be personalized to their SCI signature (age, medical history, level, completeness, and mechanism of injury).

Practical Implications

Targeted Therapies

Treatments should be tailored to the patient’s injury based on the anatomical level.

Clinical Trial Stratification

Stratification of patients into injury-level subpopulations is being increasingly adopted in trial design.

Combinatorial Approaches

Optimal patient recovery will stem from a combinatorial treatment regimen of integrated pharmacological and rehabilitation-based strategies.

Study Limitations

  • 1
    Clinical heterogeneity of SCI pathophysiology
  • 2
    Recruitment of adequate patient numbers to reach statistical power
  • 3
    Stratified analysis is susceptible to confounding effects

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