Related Experiment Video
Updated: Aug 6, 2026
Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI
Published on: April 18, 2011
Degenerative Spinal Disease Subtypes Exhibit Distinct Gait and Neuromuscular Signatures: A Retrospective Study
Zuoran Fan1,2, Fumin Pan1,2, Jingbo Cheng1,2
1Department of Orthopedics, Xuanwu Hospital, Capital Medical University, No.45 Changchun Street, Xicheng District, Beijing 100053, China.
Study Design:
A retrospective study.
Objective:
To characterize subtype-specific gait patterns and neuromuscular adaptations in DSD using integrated 3D motion capture and surface electromyography (sEMG).
Background:
Degenerative spinal diseases (DSD), including lumbar spinal stenosis (LSS), adult spinal deformity (ASD), and cervical spondylotic myelopathy (CSM), commonly impair gait in elderly patients.
Materials And Methods:
In this retrospective cross-sectional study, 148 participants (31 ASD, 40 LSS, 35 CSM, 42 healthy controls) underwent gait analysis with a BTS motion capture system and sEMG assessment of erector spinae, multifidus, gluteus maximus, and rectus abdominis muscles. Spatiotemporal parameters, root mean square maximum (RMSmax) and median frequencies (MF) were compared across stance and swing phases. Nonparametric statistical analyses were performed with significance at P<0.05.
Results:
The study included 106 patients with degenerative spinal diseases and 42 healthy elderly controls. A three-dimensional motion capture system and surface electromyography were used to synchronously analyze complete gait cycle parameters. The results showed that compared to the HC group, all three patient groups exhibited significantly reduced gait speed, lower step frequency, prolonged double-support time, increased step width, and increased asymmetry in lower limb gait parameters (P <0.001). sEMG analysis revealed that the ASD and LSS groups had increased RMSmax values and decreased MF (P <0.001). The asymmetry indices of bilateral muscles in all three patient groups were higher than those in the HC group (P <0.001), indicating compromised neuromuscular control related to disease-specific pathology.
Conclusion:
The study systematically revealed abnormal gait parameters and distinct activation patterns of core muscles in patients with degenerative spinal conditions, along with their underlying causes. Patients in the DSD group exhibited poorer bilateral lower limb gait stability and walking speed, with different muscle activation patterns due to varying causes.
Level Of Evidence:
Level IV.
