J 2022

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, Oliver MOWFORTH, Aref-Ali GHAROONI, Lindsay TETREAULT, Aria NOURI et. al.

Basic information

Original name

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, Benjamin M (guarantor), Oliver MOWFORTH, Aref-Ali GHAROONI, Lindsay TETREAULT, Aria NOURI, Rana S DHILLON, Josef BEDNAŘÍK (203 Czech Republic, belonging to the institution), Allan R MARTIN, Adam YOUNG, Hitoshi TAKAHASHI, Timothy F BOERGER, Virginia F J NEWCOMBE, Carl Moritz ZIPSER, Patrick FREUND, Paul Aarne KOLJONEN, Ricardo RODRIGUES-PINTO, Vafa RAHIMI-MOVAGHAR, Jefferson R WILSON, Shekar N KURPAD, Michael G FEHLINGS, Brian K KWON, James S HARROP, James D GUEST, Armin CURT and Mark R N KOTTER

Edition

GLOBAL SPINE JOURNAL, LONDON, SAGE PUBLICATIONS LTD, 2022, 2192-5682

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

30210 Clinical neurology

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 2.400

RIV identification code

RIV/00216224:14110/22:00128419

Organization unit

Faculty of Medicine

UT WoS

000758327200008

Keywords in English

cervical; myelopathy; spondylosis; spondylotic; stenosis; disc herniation; ossification posterior longitudinal ligament; degeneration; disability; recovery; questionnaire

Tags

Tags

International impact, Reviewed
Změněno: 31/1/2023 09:01, Mgr. Tereza Miškechová

Abstract

V originále

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.