Breen Alan, Breen Alexander
Faculty of Science and Technology, Bournemouth University, Poole, BH12 5BB, UK.
Institute for Musculoskeletal Research and Clinical Implementation, Anglo-European College of Chiropractic, Bournemouth, BH5 2DF, UK.
Eur Spine J. 2018 Jan;27(1):145-153. doi: 10.1007/s00586-017-5155-y. Epub 2017 May 29.
Evidence of intervertebral mechanical markers in chronic, non-specific low back pain (CNSLBP) is lacking. This research used dynamic fluoroscopic studies to compare intervertebral angular motion sharing inequality and variability (MSI and MSV) during continuous lumbar motion in CNSLBP patients and controls. Passive recumbent and active standing protocols were used and the relationships of these variables to age and disc degeneration were assessed.
Twenty patients with CNSLBP and 20 matched controls received quantitative fluoroscopic lumbar spine examinations using a standardised protocol for data collection and image analysis. Composite disc degeneration (CDD) scores comprising the sum of Kellgren and Lawrence grades from L2-S1 were obtained. Indices of intervertebral motion sharing inequality (MSI) and variability (MSV) were derived and expressed in units of proportion of lumbar range of motion from outward and return motion sequences during lying (passive) and standing (active) lumbar bending and compared between patients and controls. Relationships between MSI, MSV, age and CDD were assessed by linear correlation.
MSI was significantly greater in the patients throughout the intervertebral motion sequences of recumbent flexion (0.29 vs. 0.22, p = 0.02) and when flexion, extension, left and right motion were combined to give a composite measure (1.40 vs. 0.92, p = 0.04). MSI correlated substantially with age (R = 0.85, p = 0.004) and CDD (R = 0.70, p = 0.03) in lying passive investigations in patients and not in controls. There were also substantial correlations between MSV and age (R = 0.77, p = 0.01) and CDD (R = 0.85, p = 0.004) in standing flexion in patients and not in controls.
Greater inequality and variability of motion sharing was found in patients with CNSLBP than in controls, confirming previous studies and suggesting a biomechanical marker for the disorder at intervertebral level. The relationship between disc degeneration and MSI was augmented in patients, but not in controls during passive motion and similarly for MSV during active motion, suggesting links between in vivo disc mechanics and pain generation.
慢性非特异性下腰痛(CNSLBP)中缺乏椎间力学标志物的证据。本研究采用动态荧光透视研究,比较CNSLBP患者和对照组在持续腰椎运动过程中的椎间角运动分担不平等和变异性(MSI和MSV)。采用被动卧位和主动站立方案,并评估这些变量与年龄和椎间盘退变的关系。
20例CNSLBP患者和20例匹配的对照组接受了定量荧光透视腰椎检查,采用标准化方案进行数据收集和图像分析。获得包括L2-S1节段Kellgren和Lawrence分级总和的综合椎间盘退变(CDD)评分。得出椎间运动分担不平等(MSI)和变异性(MSV)指数,并以卧位(被动)和站立位(主动)腰椎屈伸过程中向外和返回运动序列的腰椎活动范围比例为单位表示,比较患者和对照组之间的差异。通过线性相关分析评估MSI、MSV、年龄和CDD之间的关系。
在患者中,卧位屈曲的整个椎间运动序列中MSI显著更高(0.29对0.22,p = 0.02),当将屈曲、伸展、左右运动合并为一个综合测量值时也是如此(1.40对0.92,p = 0.04)。在患者的卧位被动检查中,MSI与年龄(R = 0.85,p = 0.004)和CDD(R = 0.70,p = 0.03)显著相关,而在对照组中不相关。在患者的站立位屈曲中,MSV与年龄(R = 0.77,p = 0.01)和CDD(R = 0.85,p = 0.004)也显著相关,而在对照组中不相关。
与对照组相比,CNSLBP患者的运动分担不平等和变异性更大,证实了先前的研究,并提示在椎间水平存在该疾病的生物力学标志物。在被动运动期间,患者椎间盘退变与MSI之间的关系增强,而在对照组中未增强,在主动运动期间MSV也是如此,提示体内椎间盘力学与疼痛产生之间存在联系。