# Comparing Electromyographic Muscle Activities and Kinematics During Sit-to-Stand Transitions in Patients with Adult Spinal Deformity Versus Healthy Controls

**Authors:** Yukako Hayamizu, Tetsuyuki Nagafusa, Kumi Sasaki, Masaaki Nagashima, Katsuya Yamauchi, Tomohiko Hasegawa, Go Yoshida, Tomohiro Banno, Hideyuki Arima, Shin Oe, Tomohiro Yamada, Yukihiro Matsuyama, Yu Yamato

PMC · DOI: 10.3390/jcm14072514 · 2025-04-07

## TL;DR

This study compares muscle activity and movement during sit-to-stand transitions in people with adult spinal deformity and healthy individuals, revealing differences in muscle use and motion.

## Contribution

The study provides new insights into neuromuscular and biomechanical adaptations during sit-to-stand transitions in adult spinal deformity patients.

## Key findings

- ASD patients showed increased muscle activation in the biceps femoris and soleus during sit-to-stand transitions.
- ASD patients exhibited greater joint motion and longer phase durations compared to healthy controls.
- The findings suggest neuromuscular and biomechanical differences in ASD patients during STS transitions.

## Abstract

Background/Objectives: Adult spinal deformity (ASD) affects sit-to-stand (STS) transitions due to abnormal spinal alignment, influencing muscle function. This study investigated lower-extremity electromyographic activity and kinematic parameters during STS transitions in ASD patients. Methods: A cross-sectional study was conducted with ASD patients scheduled for corrective surgery. The STS task was divided into three phases, and electromyographic activity, temporal parameters, and joint kinematics were compared between ASD patients and controls. Surface electromyography measured muscle activity, and a high-speed camera recorded phase durations and joint movements. Results: Compared to 17 controls, 17 ASD patients exhibited significantly increased %MVIC (ASD, controls, p-value) in the biceps femoris during the flexion momentum phase (23.7 ± 26.5, 12.3 ± 8.6, p = 0.048) and extension phase (48.6 ± 25.8, 32.8 ± 40.5, p = 0.011), and in the soleus during the flexion momentum phase (16.2 ± 7.5, 8.5 ± 2.9, p = 0.001). The ASD group also showed greater joint motion and longer phase durations during STS transitions. Conclusions: ASD patients display increased lower limb muscle activation, prolonged phase durations, and more joint motion during STS transitions. These findings highlight neuromuscular and biomechanical differences, though whether these are pathological, adaptive, or compensatory remains unclear.

## Full-text entities

- **Diseases:** abnormal (MESH:D000014), Spinal Deformity (MESH:D013122), ASD (MESH:D009134)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11989561/full.md

---
Source: https://tomesphere.com/paper/PMC11989561