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A New Framework for Investigating the Biological Basis of Degenerative Cervical Myelopathy [AO Spine RECODE-DCM Research Priority Number 5]: Mechanical Stress, Vulnerability and Time.
Davies, Benjamin M; Mowforth, Oliver; Gharooni, Aref-Ali; Tetreault, Lindsay; Nouri, Aria; Dhillon, Rana S; Bednarik, Josef; Martin, Allan R; Young, Adam; Takahashi, Hitoshi; Boerger, Timothy F; Newcombe, Virginia Fj; Zipser, Carl Moritz; Freund, Patrick; Koljonen, Paul Aarne; Rodrigues-Pinto, Ricardo; Rahimi-Movaghar, Vafa; Wilson, Jefferson R; Kurpad, Shekar N; Fehlings, Michael G; Kwon, Brian K; Harrop, James S; Guest, James D; Curt, Armin; Kotter, Mark R N.
Afiliación
  • Davies BM; Department of Neurosurgery, 2152University of Cambridge, Cambridge, UK.
  • Mowforth O; Department of Neurosurgery, 2152University of Cambridge, Cambridge, UK.
  • Gharooni AA; Department of Neurosurgery, 2152University of Cambridge, Cambridge, UK.
  • Tetreault L; New York University, Langone Health, Graduate Medical Education, 5894Department of Neurology, New York, NY, USA.
  • Nouri A; Division of Neurosurgery, Geneva University Hospitals, 27230University of Geneva, Genève, Switzerland.
  • Dhillon RS; Department of Neurosurgery, 60078St Vincent's Hospital Melbourne, Fitzroy, VIC, Australia.
  • Bednarik J; Department of Neurology, University Hospital Brno and Faculty of Medicine, 37748Masaryk University, Brno, Czech Republic.
  • Martin AR; Department of Neurosurgery, 8789University of California Davis, Sacramento, CA, USA.
  • Young A; Department of Neurosurgery, 2152University of Cambridge, Cambridge, UK.
  • Takahashi H; Department of Pathology, Brain Research Institute, 12978Niigata University, Niigata, Japan.
  • Boerger TF; Department of Neurosurgery, 5506Medical College of Wisconsin, Wauwatosa, WI, USA.
  • Newcombe VF; Division of Anaesthesia, Department of Medicine, 2152University of Cambridge, Cambridge, UK.
  • Zipser CM; University Spine Center, 31031Balgrist University Hospital, Zurich, Switzerland.
  • Freund P; University Spine Center, 31031Balgrist University Hospital, Zurich, Switzerland.
  • Koljonen PA; Department of Orthopaedics and Traumatology, Li Ka Shing Faculty of Medicine, 25809The University of Hong Kong, Hong Kong, China.
  • Rodrigues-Pinto R; Spinal Unit (UVM), Department of Orthopaedics, 112085Centro Hospitalar Universitário do Porto - Hospital de Santo António, Porto, Portugal.
  • Rahimi-Movaghar V; 89239Instituto de Ciências Biomédicas Abel Salazar, Porto, Portugal.
  • Wilson JR; Department of Neurosurgery, Sina Trauma and Surgery Research Center, 48439Tehran University of Medical Sciences, Tehran, Iran.
  • Kurpad SN; Division of Neurosurgery, Department of Surgery, 7938University of Toronto, Toronto, ON, Canada.
  • Fehlings MG; Department of Neurosurgery, 5506Medical College of Wisconsin, Wauwatosa, WI, USA.
  • Kwon BK; Division of Neurosurgery, Department of Surgery, 7938University of Toronto, Toronto, ON, Canada.
  • Harrop JS; Vancouver Spine Surgery Institute, Department of Orthopedics, The University of British Columbia, Vancouver, BC, Canada.
  • Guest JD; Department of Neurological Surgery, 6559Thomas Jefferson University, Philadelphia, PA, USA.
  • Curt A; Department of Neurosurgery and the Miami Project to Cure Paralysis, The Miller School of Medicine, 12235University of Miami, Miami, FL, USA.
  • Kotter MRN; University Spine Center, 31031Balgrist University Hospital, Zurich, Switzerland.
Global Spine J ; 12(1_suppl): 78S-96S, 2022 Feb.
Article en En | MEDLINE | ID: mdl-35174728
STUDY DESIGN: Literature Review (Narrative). OBJECTIVE: To propose a new framework, to support the investigation and understanding of the pathobiology of DCM, AO Spine RECODE-DCM research priority number 5. METHODS: Degenerative cervical myelopathy is a common and disabling spinal cord disorder. In this perspective, we review key knowledge gaps between the clinical phenotype and our biological models. We then propose a reappraisal of the key driving forces behind DCM and an individual's susceptibility, including the proposal of a new framework. RESULTS: Present pathobiological and mechanistic knowledge does not adequately explain the disease phenotype; why only a subset of patients with visualized cord compression show clinical myelopathy, and the amount of cord compression only weakly correlates with disability. We propose that DCM is better represented as a function of several interacting mechanical forces, such as shear, tension and compression, alongside an individual's vulnerability to spinal cord injury, influenced by factors such as age, genetics, their cardiovascular, gastrointestinal and nervous system status, and time. CONCLUSION: Understanding the disease pathobiology is a fundamental research priority. We believe a framework of mechanical stress, vulnerability, and time may better represent the disease as a whole. Whilst this remains theoretical, we hope that at the very least it will inspire new avenues of research that better encapsulate the full spectrum of disease.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Global Spine J Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Global Spine J Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido