Degenerative cervical myelopathy: Where have we been? Where are we now? Where are we going?

被引:0
|
作者
Nader Hejrati
Karlo Pedro
Mohammed Ali Alvi
Ayesha Quddusi
Michael G. Fehlings
机构
[1] Krembil Research Institute,Division of Genetics and Development
[2] Toronto Western Hospital,Division of Neurosurgery and Spine Program, Department of Surgery
[3] University Health Network,Institute of Medical Science
[4] University of Toronto,undefined
[5] University of Toronto,undefined
来源
Acta Neurochirurgica | 2023年 / 165卷
关键词
Degenerative cervical myelopathy; Cervical spondylotic myelopathy; Ossification of the posterior longitudinal ligament; RECODE-DCM; Neuroprotection;
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学科分类号
摘要
Degenerative cervical myelopathy (DCM), a recently coined term, encompasses a group of age-related and genetically associated pathologies that affect the cervical spine, including cervical spondylotic myelopathy and ossification of the posterior longitudinal ligament (OPLL). Given the significant contribution of DCM to global disease and disability, there are worldwide efforts to promote research and innovation in this area. An AO Spine effort termed ‘RECODE-DCM’ was initiated to create an international multistakeholder consensus group, involving patients, caregivers, physicians and researchers, to focus on launching actionable discourse on DCM. In order to improve the management, treatment and results for DCM, the RECODE-DCM consensus group recently identified ten priority areas for translational research. The current article summarizes recent advancements in the field of DCM. We first discuss the comprehensive definition recently refined by the RECODE-DCM group, including steps taken to arrive at this definition and the supporting rationale. We then provide an overview of the recent advancements in our understanding of the pathophysiology of DCM and modalities to clinically assess and diagnose DCM. A focus will be set on advanced imaging techniques that may offer the opportunity to improve characterization and diagnosis of DCM. A summary of treatment modalities, including surgical and nonoperative options, is then provided along with future neuroprotective and neuroregenerative strategies. This review concludes with final remarks pertaining to the genetics involved in DCM and the opportunity to leverage this knowledge toward a personalized medicine approach.
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页码:1105 / 1119
页数:14
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