He Zhongyuan, Tung Nguyen Tran Canh, Makino Hiroto, Yasuda Taketoshi, Seki Shoji, Suzuki Kayo, Watanabe Kenta, Futakawa Hayato, Kamei Katsuhiko, Kawaguchi Yoshiharu
Department of Orthopaedic Surgery, Faculty of Medicine, University of Toyama, Toyama, Japan.
Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.
Neurospine. 2023 Jun;20(2):651-661. doi: 10.14245/ns.2346124.062. Epub 2023 Jun 30.
Using segmental dynamic and static factors, we aimed to elucidate the pathogenesis and relationship between ossification of the posterior longitudinal ligament (OPLL) and the severity of cervical myelopathy.
Retrospective analysis of 163 OPLL patients' 815 segments. Imaging was used to evaluate each segmental space available for the spinal cord (SAC), OPLL diameter, type, bone space, K-line, the C2-7 Cobb angle, each segmental range of motion (ROM), and total ROM. Magnetic resonance imaging was used to evaluate spinal cord signal intensity. Patients were divided into the myelopathy group (M group) and the without myelopathy group (WM group).
Minimal SAC (p = 0.043), (C2-7) Cobb angle (p = 0.004), total ROM (p = 0.013), and local ROM (p = 0.022) were evaluated as an independent predictor of myelopathy in OPLL. Different from the previous report, the M group had a straighter whole cervical spine (p < 0.001) and poorer cervical mobility (p < 0.001) compared to the WM group. Total ROM was not always a risk factor for myelopathy, as its impact depended on SAC, when SAC > 5 mm, the incidence rate of myelopathy decreased with the increase of total ROM. Lower cervical spine (C5-6, C6-7) showing increased "Bridge-Formation," along with spinal canal stenosis and segmental instability (C2-3, C3-4) in the upper cervical spine, could cause myelopathy in M group (p < 0.05).
Cervical myelopathy is linked to the OPLL's narrowest segment and its segmental motion. The hypermobility of the C2-3 and C3-4, contributes significantly to the development of myelopathy in OPLL.
利用节段性动态和静态因素,阐明后纵韧带骨化(OPLL)的发病机制以及与脊髓型颈椎病严重程度之间的关系。
对163例OPLL患者的815个节段进行回顾性分析。采用影像学评估每个节段脊髓可用空间(SAC)、OPLL直径、类型、骨间隙、K线、C2-7 Cobb角、每个节段的活动度(ROM)以及总ROM。采用磁共振成像评估脊髓信号强度。将患者分为脊髓型颈椎病组(M组)和非脊髓型颈椎病组(WM组)。
最小SAC(p = 0.043)、(C2-7)Cobb角(p = 0.004)、总ROM(p = 0.013)和局部ROM(p = 0.022)被评估为OPLL中脊髓型颈椎病的独立预测因素。与之前的报告不同,与WM组相比,M组的整个颈椎更直(p < 0.001)且颈椎活动度更差(p < 0.001)。总ROM并不总是脊髓型颈椎病的危险因素,因为其影响取决于SAC,当SAC > 5 mm时,脊髓型颈椎病的发病率随总ROM的增加而降低。下颈椎(C5-6、C6-7)显示“桥形成”增加,同时上颈椎出现椎管狭窄和节段性不稳定(C2-3、C3-4),可导致M组发生脊髓型颈椎病(p < 0.05)。
脊髓型颈椎病与OPLL最狭窄节段及其节段运动有关。C2-3和C3-4的活动度过高显著促成了OPLL中脊髓型颈椎病的发生。