Fatigue-induced biomechanical decoupling at L4-S1 discs: mechanism of disc degeneration in chronic low back pain

疲劳引起的L4-S1椎间盘生物力学解耦:慢性腰痛中椎间盘退变的机制

阅读:1

Abstract

OBJECTIVE: This study aims to quantitatively compare segment-specific disc kinematics, height changes, and strain patterns in the lumbar spine between patients with chronic low back pain (CLBP) and asymptomatic controls during weight-bearing flexion-extension, before and after fatigue loading. METHODS: A total of 29 patients with CLBP and 24 asymptomatic controls were included. All participants underwent dual fluoroscopic imaging system (DFIS) and computed tomography (CT) imaging. Weight-bearing kinematic sequences from maximum extension to approximately 45° flexion were captured pre- and post-fatigue. A validated geometric deformation model based on supine CT scans was used to quantify intervertebral kinematics from L1 to S1. Disc height variations and strain (axial and shear) were computed using computational morphometry and kinematic correspondence tracking. Statistical analyses included paired and independent t-tests for within- and between-group comparisons, with significance set at p < 0.05. RESULTS: Computational morphometry revealed distinct degenerative features associated with CLBP. Compared with controls, L4/5 discs in CLBP patients showed significantly reduced baseline height (p < 0.05), which may indicate a predisposition to early degeneration. At L5/S1, disc height was significantly reduced after fatigue loading across all postures in the CLBP group (p < 0.01), a change not observed in controls. Strain analysis demonstrated segment-dependent alterations in mechanical behavior. During flexion, both groups exhibited posterior tensile and anterior compressive strains from L4 to S1. However, after fatigue, CLBP patients developed a distinct strain pattern at L5/S1, characterized by high compressive strain and reduced shear strain. More broadly, fatigue loading in CLBP patients led to impaired shear strain dissipation and accumulation of compressive strain within the L4–S1 segments. In contrast, the upper lumbar segments (L1–L3) in both groups maintained physiological strain gradients that were unaffected by fatigue. CONCLUSIONS: This study provides in vivo evidence of fatigue-induced biomechanical alterations in the L4–S1 discs of CLBP patients, marked by increased compressive strain and reduced capacity for shear strain redistribution. The preserved biomechanical behavior in the upper lumbar segments underscores the particular vulnerability of the lumbosacral junction to mechanical deficits. These findings support the value of segment-specific biomechanical assessment for identifying early degenerative changes and inform the development of targeted load-management strategies in CLBP. However, further research is needed to account for potential confounding variables and to validate these observations in larger cohorts. TRIAL REGISTRATION: Chinese Clinical Trial Registry Registration number ChiCTR2000036039. Registered 21 August 2020.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。