Frontiers in Neurology (Feb 2024)

Voxel- and tensor-based morphometry with machine learning techniques identifying characteristic brain impairment in patients with cervical spondylotic myelopathy

  • Yang Wang,
  • Yang Wang,
  • Rui Zhao,
  • Dan Zhu,
  • Dan Zhu,
  • Xiuwei Fu,
  • Xiuwei Fu,
  • Fengyu Sun,
  • Yuezeng Cai,
  • Juanwei Ma,
  • Juanwei Ma,
  • Xing Guo,
  • Jing Zhang,
  • Jing Zhang,
  • Yuan Xue,
  • Yuan Xue

DOI
https://doi.org/10.3389/fneur.2024.1267349
Journal volume & issue
Vol. 15

Abstract

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AimThe diagnosis of cervical spondylotic myelopathy (CSM) relies on several methods, including x-rays, computed tomography, and magnetic resonance imaging (MRI). Although MRI is the most useful diagnostic tool, strategies to improve the precise and independent diagnosis of CSM using novel MRI imaging techniques are urgently needed. This study aimed to explore potential brain biomarkers to improve the precise diagnosis of CSM through the combination of voxel-based morphometry (VBM) and tensor-based morphometry (TBM) with machine learning techniques.MethodsIn this retrospective study, 57 patients with CSM and 57 healthy controls (HCs) were enrolled. The structural changes in the gray matter volume and white matter volume were determined by VBM. Gray and white matter deformations were measured by TBM. The support vector machine (SVM) was used for the classification of CSM patients from HCs based on the structural features of VBM and TBM.ResultsCSM patients exhibited characteristic structural abnormalities in the sensorimotor, visual, cognitive, and subcortical regions, as well as in the anterior corona radiata and the corpus callosum [P < 0.05, false discovery rate (FDR) corrected]. A multivariate pattern classification analysis revealed that VBM and TBM could successfully identify CSM patients and HCs [classification accuracy: 81.58%, area under the curve (AUC): 0.85; P < 0.005, Bonferroni corrected] through characteristic gray matter and white matter impairments.ConclusionCSM may cause widespread and remote impairments in brain structures. This study provided a valuable reference for developing novel diagnostic strategies to identify CSM.

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