Neurospine.  2024 Jun;21(2):375-400. 10.14245/ns.2448140.070.

Pharmacological Treatment of Degenerative Cervical Myelopathy: A Critical Review of Current Evidence

Affiliations
  • 1Faculty of Medicine, University of Montreal, Montreal, QC, Canada
  • 2Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada
  • 3Spinal Surgery Unit, Swansea Bay University Health Board, Swansea, UK
  • 4Division of Orthopaedic Surgery, McGill University, Montreal, QC, Canada
  • 5First Department of Orthopaedic Surgery NKUA, “ATTIKON” University General Hospital, Athens, Greece
  • 6Winnipeg Spine Program, University of Manitoba, Winnipeg, MB, Canada
  • 7Neurosurgery Department, Sanford Brain & Spine Center, Fargo, ND, USA
  • 8Department of Neurosurgery, Zucker School of Medicine at Hofstra/Northwell, Bay Shore, NY, USA
  • 9Edinburgh Spinal Surgery Outcomes Study Group, Department of Neurosurgery, Royal Infirmary, Edinburgh, UK

Abstract

Degenerative cervical myelopathy (DCM) is the leading cause of spinal cord dysfunction in adults, representing substantial morbidity and significant financial and resource burdens. Typically, patients with progressive DCM will eventually receive surgical treatment. Nonetheless, despite advancements in pharmacotherapeutics, evidence for pharmacological therapy remains limited. Health professionals from various fields would find interest in pharmacological agents that could benefit patients with mild DCM or enhance surgical outcomes. This review aims to consolidate all clinical and experimental evidence on the pharmacological treatment of DCM. We conducted a comprehensive narrative review that presents all pharmacological agents that have been investigated for DCM treatment in both humans and animal models. Riluzole exhibits effectiveness solely in rat models, but not in treating mild DCM in humans. Cerebrolysin emerges as a potential neuroprotective agent for myelopathy in animals but had contradictory results in clinical trials. Limaprost alfadex demonstrates motor function improvement in animal models and exhibits promising outcomes in a small clinical trial. Glucocorticoids not only fail to provide clinical benefits but may also lead to adverse events. Cilostazol, anti-Fas ligand antibody, and Jingshu Keli display promise in animal studies, while erythropoietin, granulocyte colony-stimulating factor and limaprost alfadex exhibit potential in both animal and human research. Existing evidence mainly rests on weak clinical data and animal experimentation. Current pharmacological efforts target ion channels, stem cell differentiation, inflammatory, vascular, and apoptotic pathways. The inherent nature and pathogenesis of DCM offer substantial prospects for developing neurodegenerative or neuroprotective therapies capable of altering disease progression, potentially delaying surgical intervention, and optimizing outcomes for those undergoing surgical decompression.

Keyword

Intervertebral disc degeneration; Cervical cord; Erythropoietin; limaprost-alfadex; Glucocorticoids; Riluzole
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