Automatic estimation of brain parenchymal fraction in patients with multple sclerosis: a comparison between synthetic

Ilyas Yazici1, Britta Krieger1, Barbara Bellenberg1

  • 1Institute of Neuroradiology, St. Josef Hospital, Ruhr-University Bochum, Gudrunstrasse 56, 44791, Bochum, Germany.

Neuroradiology
|December 19, 2023
PubMed
Abstract

Insights

Synthetic MRI (SyMRI) shows good agreement for brain parenchymal fraction (BPF) in multiple sclerosis (MS) patients, despite some overestimation compared to FSL software. SyMRI is suitable for quantifying MS-related brain atrophy.

Area of Science:

  • Neuroimaging
  • Radiology
  • Biomedical Engineering

Background:

  • Multiple Sclerosis (MS) is a chronic neurological disease characterized by progressive brain atrophy.
  • Accurate quantification of brain volume changes is crucial for monitoring MS progression and treatment efficacy.
  • Synthetic Magnetic Resonance Imaging (SyMRI) offers potential for rapid and quantitative tissue characterization.

Purpose of the Study:

  • To validate brain parenchymal fraction (BPF) estimation using SyMRI against established FMRIB Software Library (FSL) tools in MS patients.
  • To compare cross-sectional and longitudinal brain volume changes derived from SyMRI and FSL.
  • To assess SyMRI's suitability for quantifying disease-specific atrophy in MS.

Main Methods:

  • Cross-sectional comparison of BPF and grey/white matter volumes between SyMRI and FSL-SIENAX in 216 MS patients and 28 controls.
  • Longitudinal analysis of brain volume changes using SyMRI and FSL-SIENA in 35 MS patients.
  • Statistical analysis including correlation, intra-class correlation coefficients, and Bland-Altman plots.

Main Results:

  • Strong correlations observed between SyMRI and FSL for estimated brain volumes.
  • SyMRI showed a systematic bias, overestimating grey matter and BPF compared to FSL-SIENAX.
  • Excellent agreement for grey matter and good agreement for BPF and white matter volumes were found.
  • Longitudinal analyses indicated higher atrophy rates with SyMRI but demonstrated robust correlation and good agreement with FSL-SIENA.

Conclusions:

  • BPF derived from SyMRI and FSL-SIENAX are not directly interchangeable due to SyMRI's overestimation and variability.
  • Despite systematic bias, SyMRI demonstrates satisfactory consistency and correlation with FSL.
  • SyMRI is a suitable tool for quantifying disease-specific brain atrophy in multiple sclerosis.

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