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
Department of Neurosurgery, 2152University of Cambridge, Cambridge, UK.
New York University, Langone Health, Graduate Medical Education, 5894Department of Neurology, New York, NY, USA.
Global Spine J. 2022 Feb;12(1_suppl):78S-96S. doi: 10.1177/21925682211057546.
Literature Review (Narrative).
To propose a new framework, to support the investigation and understanding of the pathobiology of DCM, AO Spine RECODE-DCM research priority number 5.
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.
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.
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.
文献综述(叙述性)。
提出一个新框架,以支持对扩张型心肌病(DCM)病理生物学的研究和理解,这是AO脊柱再编码-DCM研究优先级的第5项。
退行性颈椎脊髓病是一种常见且致残的脊髓疾病。从这个角度出发,我们回顾了临床表型与我们的生物学模型之间的关键知识空白。然后,我们对DCM背后的关键驱动力以及个体易感性提出重新评估,包括提出一个新框架。
目前的病理生物学和机制知识并不能充分解释疾病表型;为什么只有一部分脊髓受压可视化的患者表现出临床脊髓病,而且脊髓受压程度与残疾程度仅呈弱相关。我们提出,DCM更好地表现为几种相互作用的机械力的函数,如剪切力、张力和压力,同时还有个体对脊髓损伤的易感性,这受年龄、遗传学、心血管、胃肠道和神经系统状态以及时间等因素影响。
了解疾病病理生物学是一项基本的研究重点。我们相信,机械应力、易感性和时间的框架可能更好地整体呈现该疾病。虽然这仍然是理论性的,但我们希望至少它能激发新的研究途径,更好地涵盖疾病的全貌。