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Item Type: | Article |
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Title: | Paramagnetic rims are a promising diagnostic imaging biomarker in multiple sclerosis |
Creators Name: | Meaton, I. and Altokhis, A. and Allen, C.M. and Clarke, M.A. and Sinnecker, T. and Meier, D. and Enzinger, C. and Calabrese, M. and De Stefano, N. and Pitiot, A. and Giorgio, A. and Schoonheim, M.M. and Paul, F. and Pawlak, M.A. and Schmidt, R. and Granziera, C. and Kappos, L. and Montalban, X. and Rovira, À. and Wuerfel, Jens and Evangelou, N. |
Abstract: | BACKGROUND: White matter lesions (WMLs) on brain magnetic resonance imaging (MRI) in multiple sclerosis (MS) may contribute to misdiagnosis. In chronic active lesions, peripheral iron-laden macrophages appear as paramagnetic rim lesions (PRLs). OBJECTIVE: To evaluate the sensitivity and specificity of PRLs in differentiating MS from mimics using clinical 3T MRI scanners. METHOD: This retrospective international study reviewed MRI scans of patients with MS (n = 254), MS mimics (n = 91) and older healthy controls (n = 217). WMLs, detected using fluid-attenuated inversion recovery MRI, were analysed with phase-sensitive imaging. Sensitivity and specificity were assessed for PRLs. RESULTS: At least one PRL was found in 22.9% of MS and 26.1% of clinically isolated syndrome (CIS) patients. Only one PRL was found elsewhere. The identification of ?1 PRL was the optimal cut-off and had high specificity (99.7%, confidence interval (CI) = 98.20%-99.99%) when distinguishing MS and CIS from mimics and healthy controls, but lower sensitivity (24.0%, CI = 18.9%-36.6%). All patients with a PRL showing a central vein sign (CVS) in the same lesion (n = 54) had MS or CIS, giving a specificity of 100% (CI = 98.8%-100.0%) but equally low sensitivity (21.3%, CI = 16.4%-26.81%). CONCLUSION: PRLs may reduce diagnostic uncertainty in MS by being a highly specific imaging diagnostic biomarker, especially when used in conjunction with the CVS. |
Keywords: | Multiple Sclerosis, MRI, CIS, Biomarkers |
Source: | Multiple Sclerosis Journal |
ISSN: | 1352-4585 |
Publisher: | Sage Publications |
Volume: | 28 |
Number: | 14 |
Page Range: | 2212-2220 |
Date: | December 2022 |
Official Publication: | https://doi.org/10.1177/13524585221118677 |
PubMed: | View item in PubMed |
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