What is the potential of paramagnetic rim lesions as diagnostic indicators in multiple sclerosis?

Lucia Moiola, Maria Sofia Martire, Maria Assunta Rocca, Massimo Filippi, Martina Absinta

Journal: Expert review of neurotherapeutics 2022;22(10):829-837

PMID: 36342396

Abstract

INTRODUCTION

In multiple sclerosis (MS), paramagnetic rim lesions (PRLs) on MRI identify a subset of chronic active lesions (CALs), which have been linked through clinical and pathological studies to more severe disease course and greater disability accumulation. Beside their prognostic relevance, increasing evidence supports the use of PRL as a diagnostic biomarker.

AREAS COVERED

This review summarizes the most recent updates regarding the MRI pathophysiology of PRL, their prevalence in MS (by clinical phenotypes) vs mimicking conditions, and their potential role as diagnostic MS biomarkers. We searched PubMed with terms including 'multiple sclerosis' AND 'paramagnetic rim lesions' OR 'iron rim lesions' OR 'rim lesions' for manuscripts published between January 2008 and July 2022.

EXPERT OPINION

Current research suggests that PRL can improve the diagnostic specificity and the overall accuracy of MS diagnosis when used together with the dissemination in space MRI criteria and the central vein sign. Nevertheless, future prospective multicenter studies should further define the real-world prevalence and specificity of PRL. International guidelines are needed to establish methodological criteria for PRL identification before its implementation into clinical practice.

Address: Neurology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Division of Neuroscience, Vita-Salute San Raffaele University, Milan, Italy.; Neurophysiology Service, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Neurorehabilitation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
MeSH Terms: Humans, Sclerosis
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