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Comparative evaluation of EPI and SWI for the assessment of PRL and CVS in Multiple Sclerosis
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Abstract
Introduction
The 2024 McDonald criteria incorporate the central vein sign (CVS) and paramagnetic rim lesions (PRL) as supportive imaging biomarkers for MS diagnosis. While susceptibility-weighted-imaging (SWI) and T2*-weighted echo-planar-imaging (EPI) are generally used to assess CVS/PRL, their relative performance remains unclear. This study compared high-resolution isotropic-T2*-EPI with non-isotropic SWI for CVS/PRL detection.
Materials and Methods
In this multi-centre study, 21 patients with MS underwent harmonized 3T-MRI including EPI and SWI. CVS and PRL were evaluated according to NAIMS criteria. Whole-brain and controlled lesion analyses on 120 pre-selected lesions were performed independently for each contrast, with EPI serving as reference standard.
Results
In whole-brain analyses, SWI showed good sensitivity for CVS eligibility and positivity (AC1=0.68-0.78) but significant directional disagreement with EPI (p<0.0001). Discrepancies were primarily attributed to limited lesion-parenchyma contrast and venous visibility on SWI, which improved using low-flip-angle SWI. Controlled lesion analyses supported these observations. For PRL, SWI demonstrated high sensitivity (88%) and precision (97%) compared to EPI, though systematic bias persisted (p<0.001). Controlled lesion analyses showed more balanced, albeit moderate performance.
Conclusion
SWI diverged systematically from EPI for CVS and PRL detection. When available, EPI should be preferred, while optimised low-flip-angle SWI may serve as an alternative to conventional SWI.
Title: Comparative evaluation of EPI and SWI for the assessment of PRL and CVS in Multiple Sclerosis
Description:
Abstract
Introduction
The 2024 McDonald criteria incorporate the central vein sign (CVS) and paramagnetic rim lesions (PRL) as supportive imaging biomarkers for MS diagnosis.
While susceptibility-weighted-imaging (SWI) and T2*-weighted echo-planar-imaging (EPI) are generally used to assess CVS/PRL, their relative performance remains unclear.
This study compared high-resolution isotropic-T2*-EPI with non-isotropic SWI for CVS/PRL detection.
Materials and Methods
In this multi-centre study, 21 patients with MS underwent harmonized 3T-MRI including EPI and SWI.
CVS and PRL were evaluated according to NAIMS criteria.
Whole-brain and controlled lesion analyses on 120 pre-selected lesions were performed independently for each contrast, with EPI serving as reference standard.
Results
In whole-brain analyses, SWI showed good sensitivity for CVS eligibility and positivity (AC1=0.
68-0.
78) but significant directional disagreement with EPI (p<0.
0001).
Discrepancies were primarily attributed to limited lesion-parenchyma contrast and venous visibility on SWI, which improved using low-flip-angle SWI.
Controlled lesion analyses supported these observations.
For PRL, SWI demonstrated high sensitivity (88%) and precision (97%) compared to EPI, though systematic bias persisted (p<0.
001).
Controlled lesion analyses showed more balanced, albeit moderate performance.
Conclusion
SWI diverged systematically from EPI for CVS and PRL detection.
When available, EPI should be preferred, while optimised low-flip-angle SWI may serve as an alternative to conventional SWI.
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