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Individuals With and Without Low Back Pain Use Different Motor Control Strategies to Achieve Spinal Stiffness During
The Journal of Orthopaedic and Sports Physical Therapy
|August 6, 2019
Summary
Individuals with low back pain (LBP) exhibit altered muscle activation patterns during the prone instability test, using fewer muscle synergies than healthy controls. This suggests a potentially maladaptive stabilization strategy in LBP patients.
Area of Science:
- Biomechanics
- Motor Control
- Orthopedics
Background:
- The prone instability test is a clinical tool to identify low back pain (LBP) patients who may benefit from trunk stabilization exercises.
- The underlying mechanism of pain reduction during this test, specifically muscle activation and spinal stiffness, requires further investigation.
Purpose of the Study:
- To compare changes in pain and spinal stiffness across different positions of the prone instability test.
- To analyze and contrast trunk and limb muscle activation patterns during the leg-raising component of the test in individuals with and without LBP.
Main Methods:
- A case-control laboratory study involving 10 participants with LBP and 10 without.
- Spinal stiffness was quantified using a beam-bending model and 3D kinematic analysis.
- Surface electromyography (sEMG) captured muscle activity, with principal-component analysis used to identify muscle synergies.
Main Results:
- Spinal stiffness increased significantly across test positions in all participants.
- Participants with LBP reported reduced pain during the test.
- No significant difference in spinal stiffness was observed between groups during leg raising.
- Individuals without LBP utilized 3 distinct muscle synergies, while those with LBP employed 2, indicating a simpler activation pattern.
Conclusions:
- While spinal stiffness increases in all individuals during the prone instability test, those with LBP demonstrate a less differentiated muscle synergy pattern.
- The observed global stabilization strategy in LBP participants may represent a maladaptive response to enhance spinal stability.
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