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Interscanner variation in brain MR lesion load measurements in multiple sclerosis using conventional spin-echo, rapid

M Filippi1, M A Rocca, C Gasperini

  • 1Department of Neuroscience, Scientific Institute Ospedale San Raffaele, Milan, Italy.

Abstract

Insights

Comparing magnetic resonance imaging (MRI) sequences for multiple sclerosis (MS) lesion volume measurement reveals that different scanners significantly impact results. Newer sequences like fast fluid-attenuated inversion recovery (fast-FLAIR) show greater variability, necessitating standardization for clinical trials.

Area of Science:

  • Neuroimaging
  • Radiology
  • Medical Physics

Background:

  • Multiple sclerosis (MS) diagnosis and monitoring rely on detecting brain abnormalities using magnetic resonance imaging (MRI).
  • Various MRI pulse sequences exist for quantifying MS-related lesions, but their reproducibility across different scanners and sequences is crucial for reliable assessment.

Purpose of the Study:

  • To compare the reproducibility of brain lesion volume measurements in multiple sclerosis (MS) patients using different MRI scanners and pulse sequences.
  • To evaluate the impact of scanner variability and sequence choice on the accuracy of MS lesion load quantification.

Main Methods:

  • Nine relapsing-remitting MS patients underwent MRI scans on two different scanners.
  • Dual-echo conventional spin-echo, dual-echo rapid-acquisition relaxation-enhanced (RARE), and fast fluid-attenuated inversion recovery (fast-FLAIR) sequences were acquired.
  • Lesion volumes were assessed three times by a single observer using local thresholding.

Main Results:

  • Fast-FLAIR sequences yielded significantly higher mean lesion volumes compared to conventional spin-echo and RARE sequences.
  • Intraobserver variability was consistent across sequences and scanners (3.0%-4.2%).
  • Interscanner variability was higher than intraobserver variability, particularly for fast-FLAIR (18.5%), RARE (9.5%), and conventional spin-echo (7.4%).

Conclusions:

  • Scanner differences significantly influence MS lesion load measurements derived from MRI.
  • Newer MRI sequences, such as fast-FLAIR, are more susceptible to measurement variability.
  • Standardization of MRI sequences and protocols is essential for multi-center clinical trials involving MS patients.

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