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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.

Authors :
Davies BM
Mowforth O
Gharooni AA
Tetreault L
Nouri A
Dhillon RS
Bednarik J
Martin AR
Young A
Takahashi H
Boerger TF
Newcombe VF
Zipser CM
Freund P
Koljonen PA
Rodrigues-Pinto R
Rahimi-Movaghar V
Wilson JR
Kurpad SN
Fehlings MG
Kwon BK
Harrop JS
Guest JD
Curt A
Kotter MRN
Source :
Global spine journal [Global Spine J] 2022 Feb; Vol. 12 (1_suppl), pp. 78S-96S.
Publication Year :
2022

Abstract

Study Design: Literature Review (Narrative).<br />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.<br />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.<br />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.<br />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.

Details

Language :
English
ISSN :
2192-5682
Volume :
12
Issue :
1_suppl
Database :
MEDLINE
Journal :
Global spine journal
Publication Type :
Academic Journal
Accession number :
35174728
Full Text :
https://doi.org/10.1177/21925682211057546