Whole-brain atrophy in multiple sclerosis measured by automated versus semiautomated MR imaging segmentation

Jitendra Sharma1, Michael P Sanfilipo, Ralph H B Benedict

  • 1Buffalo Neuroimaging Analysis Center, University at Buffalo, State University of New York, Buffalo, NY, USA.

Abstract

Insights

Automated and semiautomated methods for measuring whole-brain atrophy in multiple sclerosis (MS) provide similar, interchangeable data. These techniques effectively distinguish MS patients from healthy individuals and correlate with disease severity.

Area of Science:

  • Neuroimaging
  • Medical Physics
  • Radiology

Background:

  • Whole-brain atrophy measurement in multiple sclerosis (MS) is crucial for disease monitoring.
  • Semiautomated and automated imaging techniques are increasingly used, but their comparative performance is not well-established.

Purpose of the Study:

  • To compare the reliability, sensitivity, and validity of semiautomated and automated methods for measuring brain parenchymal fraction (BPF) in MS.
  • To assess the correlation of these BPF measures with established clinical and imaging markers of MS severity.

Main Methods:

  • Brain parenchymal fraction (BPF) was measured in 52 MS patients and 17 healthy controls using four methods: semiautomated/automated segmentation with 2D/3D pulse sequences.
  • Validity was explored using linear atrophy measures, lesion volumes, and clinical data.

Main Results:

  • The 2D automated method was unreliable and excluded. The remaining three BPF methods yielded highly correlated and statistically indistinguishable results.
  • All three methods showed significantly lower BPF in MS patients compared to controls.
  • BPF measures demonstrated strong inverse correlations with ventricular width and bicaudate ratio, and moderate correlations with lesion load and disability scores.

Conclusions:

  • Semiautomated and automated BPF measurements offer similar, nearly interchangeable data for assessing whole-brain atrophy in MS.
  • These methods reliably differentiate MS patients from healthy individuals and correlate consistently with key disease variables.

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