10
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Cranial Nerve Enhancement in Multiple Sclerosis Is Associated With Younger Age at Onset and More Severe Disease

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background: The overall frequency of cranial nerve pathology, including cranial nerves other than the trigeminal nerve, as well as its relation to brainstem lesion formation on magnetic resonance imaging (MRI) and clinical correlates in multiple sclerosis (MS) is unknown.

          Objective: We aimed to determine the frequency of cranial nerve enhancement on MRI, and its association with brainstem lesion formation and clinical outcomes.

          Methods: We retrospectively analyzed, in 183 patients, (RRMS: 156, SPMS: 15, PPMS: 6, CIS: 6) 651 MRIs (76.5% on the identical scanner Siemens Trio Tim, 3T with identical MRI protocols). Frequencies of cranial nerve enhancement on post contrast T1-weighted MRIs were compared to lesion counts and the MS-severity-score.

          Results: Cranial nerve enhancement was present in 8.2% of the analyzed MS patients (oculomotor-nerve: 1.1%, trigeminal-nerve: 2.7%, abducens-nerve: 2.2%, facial-/vestibulocochlear nerve: 1.6%, vagal-nerve: 0.5%). Of those, 13% suffered from repeated episodes and 27% exhibited a cranial nerve enhancement duration of >12 months. Age at MS onset was lower in patients with cranial nerve enhancement, 23 vs. 28 years, p = 0.049. The MS-severity-score, 5.15 vs. 0.88 ( p = 0.019), the T2 brainstem-, 1 vs. 0 ( p = 0.041), and the total intracranial contrast-enhancing lesion counts, 2 vs. 0 ( p = 0.000), were higher in patients with cranial nerve enhancement, compared to age-, disease duration-, and gender- matched MS patients.

          Conclusions: Cranial nerve enhancement, present in 8.2% of our patients, was associated with a younger age at MS onset, brainstem lesions, and a more severe disease course.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: found
          • Article: not found

          Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

          There is no consensus method for determining progression of disability in patients with multiple sclerosis (MS) when each patient has had only a single assessment in the course of the disease. Using data from two large longitudinal databases, the authors tested whether cross-sectional disability assessments are representative of disease severity as a whole. An algorithm, the Multiple Sclerosis Severity Score (MSSS), which relates scores on the Expanded Disability Status Scale (EDSS) to the distribution of disability in patients with comparable disease durations, was devised and then applied to a collection of 9,892 patients from 11 countries to create the Global MSSS. In order to compare different methods of detecting such effects the authors simulated the effects of a genetic factor on disability. Cross-sectional EDSS measurements made after the first year were representative of overall disease severity. The MSSS was more powerful than the other methods the authors tested for detecting different rates of disease progression. The Multiple Sclerosis Severity Score (MSSS) is a powerful method for comparing disease progression using single assessment data. The Global MSSS can be used as a reference table for future disability comparisons. While useful for comparing groups of patients, disease fluctuation precludes its use as a predictor of future disability in an individual.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Experiments on the Section of the Glossopharyngeal and Hypoglossal Nerves of the Frog, and Observations of the Alterations Produced Thereby in the Structure of Their Primitive Fibres

            A. Waller (1850)
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Multiple sclerosis deep grey matter: the relation between demyelination, neurodegeneration, inflammation and iron

              In multiple sclerosis (MS), diffuse degenerative processes in the deep grey matter have been associated with clinical disabilities. We performed a systematic study in MS deep grey matter with a focus on the incidence and topographical distribution of lesions in relation to white matter and cortex in a total sample of 75 MS autopsy patients and 12 controls. In addition, detailed analyses of inflammation, acute axonal injury, iron deposition and oxidative stress were performed. MS deep grey matter was affected by two different processes: the formation of focal demyelinating lesions and diffuse neurodegeneration. Deep grey matter demyelination was most prominent in the caudate nucleus and hypothalamus and could already be seen in early MS stages. Lesions developed on the background of inflammation. Deep grey matter inflammation was intermediate between low inflammatory cortical lesions and active white matter lesions. Demyelination and neurodegeneration were associated with oxidative injury. Iron was stored primarily within oligodendrocytes and myelin fibres and released upon demyelination. In addition to focal demyelinated plaques, the MS deep grey matter also showed diffuse and global neurodegeneration. This was reflected by a global reduction of neuronal density, the presence of acutely injured axons, and the accumulation of oxidised phospholipids and DNA in neurons, oligodendrocytes and axons. Neurodegeneration was associated with T cell infiltration, expression of inducible nitric oxide synthase in microglia and profound accumulation of iron. Thus, both focal lesions as well as diffuse neurodegeneration in the deep grey matter appeared to contribute to the neurological disabilities of MS patients.
                Bookmark

                Author and article information

                Contributors
                Journal
                Front Neurol
                Front Neurol
                Front. Neurol.
                Frontiers in Neurology
                Frontiers Media S.A.
                1664-2295
                06 November 2019
                2019
                : 10
                : 1085
                Affiliations
                [1] 1NMR Research Unit, Department of Neuroinflammation, Faculty of Brain Science, Queen Square MS Centre, UCL Institute of Neurology, University College London , London, United Kingdom
                [2] 2Department of Biomedical Imaging and Image-Guided Therapy, Medical University Vienna , Vienna, Austria
                [3] 3Department of Neurology, University Hospital Tulln , Tulln, Austria
                [4] 4Department of Neuroradiology, Medical University of Innsbruck , AUT, Innsbruck, Austria
                [5] 5Neuroimaging Core Facility, Medical University of Innsbruck , AUT, Innsbruck, Austria
                [6] 6Department of Neurology, Medical University Vienna , Vienna, Austria
                Author notes

                Edited by: Masaaki Murakami, Hokkaido University, Japan

                Reviewed by: Izumi Kawachi, Niigata University, Japan; Jorge Tolivia, Universidad de Oviedo, Spain

                *Correspondence: Stephanie Mangesius stephanie.mangesius@ 123456i-med.ac.at

                This article was submitted to Multiple Sclerosis and Neuroimmunology, a section of the journal Frontiers in Neurology

                Article
                10.3389/fneur.2019.01085
                6851051
                31781014
                5323cd68-a27b-4754-b665-9127f0d94757
                Copyright © 2019 Haider, Chan, Olbert, Mangesius, Dal-Bianco, Leutmezer, Prayer and Thurnher.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 June 2019
                : 26 September 2019
                Page count
                Figures: 3, Tables: 4, Equations: 0, References: 26, Pages: 8, Words: 5856
                Categories
                Neurology
                Original Research

                Neurology
                multiple sclerosis,magnetic resonance imaging,contrast media,cranial nerves,brain stem,retrograde neurodegeneration

                Comments

                Comment on this article