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      Advanced MRI and staging of multiple sclerosis lesions

      research-article
      1 , 2 , 1 , 1
      Nature reviews. Neurology

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          Abstract

          Over the past few decades, MRI-based visualization of demyelinated CNS lesions has become pivotal to the diagnosis and monitoring of multiple sclerosis (MS). In this Review, we outline current efforts to correlate imaging findings with the pathology of lesion development in MS, and the pitfalls that are being encountered in this research. Multimodal imaging at high and ultra-high magnetic field strengths is yielding biologically relevant insights into the pathophysiology of blood–brain barrier dynamics and both active and chronic inflammation, as well as mechanisms of lesion healing and remyelination. Here, we parallel the results in humans with advances in imaging of a primate model of MS — experimental autoimmune encephalomyelitis (EAE) in the common marmoset — in which demyelinated lesions resemble their human counterparts far more closely than do EAE lesions in the rodent. This approach holds promise for the identification of innovative biological markers and next-generation clinical trials that will focus more on tissue protection and repair.

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          Author and article information

          Journal
          101500072
          35770
          Nat Rev Neurol
          Nat Rev Neurol
          Nature reviews. Neurology
          1759-4758
          1759-4766
          19 October 2016
          29 April 2016
          June 2016
          01 June 2017
          : 12
          : 6
          : 358-368
          Affiliations
          [1 ]Translational Neuroradiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, 10 Center Drive MSC 1400, Building 10 Room 5C103, Bethesda, Maryland 20852, USA
          [2 ]Institute of Experimental Neurology, Division of Neuroscience, San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Via Olgettina 60, 20132, Milan, Italy
          Author notes
          Correspondence to D.S.R. reichds@ 123456ninds.nih.gov
          Article
          PMC5074769 PMC5074769 5074769 nihpa823945
          10.1038/nrneurol.2016.59
          5074769
          27125632
          a275bc09-cb11-469c-91c6-4a2fac31163f
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