The fatty degeneration of the lumbar erector spinae muscles affects dynamic spinal compensation ability during gait in adult spinal deformity

Sci Rep. 2021 Sep 10;11(1):18088. doi: 10.1038/s41598-021-97358-5.

Abstract

This study aimed to investigate whether fat infiltration in lumbar paravertebral muscles assessed by magnetic resonance imaging (MRI) could be related to dynamic sagittal spino-pelvic balance during gait in adult spinal deformity (ASD). This is a retrospective analysis of 28 patients with ASD. The fat infiltration rate of lumbar erector spinae muscles, multifidus muscles and psoas major muscles was measured by T2 weighted axial MRI at L1-2 and L4-5. Dynamic sagittal spinal and pelvic angles during gait were evaluated using 3D motion analysis. The correlation between fat infiltration rate of those muscles with variations in dynamic kinematic variables while walking and static radiological parameters was analyzed. Spinal kyphosis and pelvic anteversion significantly increased during gait. Fat infiltration rate of erector spinae muscles at L1-2 was positively correlated with thoracic kyphosis (r = 0.392, p = 0.039) and pelvic tilt (r = 0.415, p = 0.028). Increase of spinal kyphosis during walking was positively correlated with fat infiltration rate of erector spinae muscles both at L1-2 (r = 0.394, p = 0.038) and L4-5 (r = 0.428, p = 0.023). Qualitative evaluation of lumbar erector spinae muscles assessed by fat infiltration rate has the potential to reflect dynamic spino-pelvic balance during gait.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Disease Management
  • Disease Susceptibility
  • Gait*
  • Humans
  • Kyphosis / diagnosis
  • Kyphosis / etiology
  • Kyphosis / physiopathology
  • Lumbosacral Region / pathology*
  • Magnetic Resonance Imaging*
  • Paraspinal Muscles / pathology*
  • Pelvis / physiopathology
  • Spinal Curvatures / diagnosis
  • Spinal Curvatures / etiology
  • Spinal Curvatures / physiopathology
  • Spinal Diseases / diagnosis
  • Spinal Diseases / etiology*
  • Spinal Diseases / physiopathology*