Literature DB >> 27009310

A practical review of the neuropathology and neuroimaging of multiple sclerosis.

Paul M Matthews1, Frederico Roncaroli2, Adam Waldman1, Maria Pia Sormani3, Nicola De Stefano4, Gavin Giovannoni5, Richard Reynolds1.   

Abstract

The variability in the severity and clinical course of multiple sclerosis (MS) has as its basis an extreme heterogeneity in the location, nature and extent of pathology in the brain and spinal cord. Understanding the underlying neuropathology and associated pathogenetic mechanisms of the disease helps to communicate the rationale for treatment and disease monitoring to patients. Neuroimaging is an important tool for this: it allows clinicians to relate neuropathological changes to clinical presentations and to monitor the course of their disease. Here, we review MS neuropathology and its imaging correlates to provide a practical guide for using MRI to assess disease severity and treatment responses. This provides a foundation for optimal management of patients based on the principle that they show 'no evidence of disease activity'. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  CLINICAL NEUROLOGY; MULTIPLE SCLEROSIS; NEUROPATHOLOGY; Neuroimaging

Mesh:

Year:  2016        PMID: 27009310     DOI: 10.1136/practneurol-2016-001381

Source DB:  PubMed          Journal:  Pract Neurol        ISSN: 1474-7758


  11 in total

1.  High-Resolution Expression Profiling of Peripheral Blood CD8+ Cells in Patients with Multiple Sclerosis Displays Fingolimod-Induced Immune Cell Redistribution.

Authors:  Luisa Roch; Michael Hecker; Jörg Friess; Ines Charlotte Angerer; Dirk Koczan; Brit Fitzner; Ina Schröder; Kristin Flechtner; Hans-Jürgen Thiesen; Stefanie Meister; Alexander Winkelmann; Uwe Klaus Zettl
Journal:  Mol Neurobiol       Date:  2016-09-08       Impact factor: 5.590

2.  Yet more evidence that myelin protons can be directly imaged with UTE sequences on a clinical 3T scanner: Bicomponent T2* analysis of native and deuterated ovine brain specimens.

Authors:  Shu-Juan Fan; Yajun Ma; Yanchun Zhu; Adam Searleman; Nikolaus M Szeverenyi; Graeme M Bydder; Jiang Du
Journal:  Magn Reson Med       Date:  2017-12-21       Impact factor: 4.668

3.  The Central Vein: FLAIR Signal Abnormalities Associated with Developmental Venous Anomalies in Patients with Multiple Sclerosis.

Authors:  D M Rogers; L M Shah; R H Wiggins
Journal:  AJNR Am J Neuroradiol       Date:  2018-10-18       Impact factor: 3.825

4.  Reduced brain atrophy rates are associated with lower risk of disability progression in patients with relapsing multiple sclerosis treated with cladribine tablets.

Authors:  Nicola De Stefano; Antonio Giorgio; Marco Battaglini; Alessandro De Leucio; Christine Hicking; Fernando Dangond; Gavin Giovannoni; Maria Pia Sormani
Journal:  Mult Scler       Date:  2017-01-31       Impact factor: 6.312

Review 5.  Cladribine tablets' potential role as a key example of selective immune reconstitution therapy in multiple sclerosis.

Authors:  Alexey N Boyko; Olga V Boyko
Journal:  Degener Neurol Neuromuscul Dis       Date:  2018-05-03

6.  Do eyes with and without optic neuritis in multiple sclerosis age equally?

Authors:  Jana Lizrova Preiningerova; Anna Grishko; Lukas Sobisek; Michaela Andelova; Barbora Benova; Karolina Kucerova; Eva Kubala Havrdova
Journal:  Neuropsychiatr Dis Treat       Date:  2018-09-05       Impact factor: 2.570

Review 7.  Spotlight on postural control in patients with multiple sclerosis.

Authors:  Luca Prosperini; Letizia Castelli
Journal:  Degener Neurol Neuromuscul Dis       Date:  2018-04-03

Review 8.  Navigating choice in multiple sclerosis management.

Authors:  Ralf A Linker; Andrew Chan
Journal:  Neurol Res Pract       Date:  2019-02-28

Review 9.  How changes in brain activity and connectivity are associated with motor performance in people with MS.

Authors:  Daniel S Peterson; Brett W Fling
Journal:  Neuroimage Clin       Date:  2017-09-28       Impact factor: 4.881

10.  Th17 cells increase in RRMS as well as in SPMS, whereas various other phenotypes of Th17 increase in RRMS only.

Authors:  S Kalra; C Lowndes; L Durant; R C Strange; A Al-Araji; Clive P Hawkins; S John Curnow
Journal:  Mult Scler J Exp Transl Clin       Date:  2020-01-28
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