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.Základní údaje
Originální název
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
Autoři
DAVIES, Benjamin M (garant), Oliver MOWFORTH, Aref-Ali GHAROONI, Lindsay TETREAULT, Aria NOURI, Rana S DHILLON, Josef BEDNAŘÍK (203 Česká republika, domácí), 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 a Mark R N KOTTER
Vydání
GLOBAL SPINE JOURNAL, LONDON, SAGE PUBLICATIONS LTD, 2022, 2192-5682
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30210 Clinical neurology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.400
Kód RIV
RIV/00216224:14110/22:00128419
Organizační jednotka
Lékařská fakulta
UT WoS
000758327200008
Klíčová slova anglicky
cervical; myelopathy; spondylosis; spondylotic; stenosis; disc herniation; ossification posterior longitudinal ligament; degeneration; disability; recovery; questionnaire
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 31. 1. 2023 09:01, Mgr. Tereza Miškechová
Anotace
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.