Literature DB >> 20847000

Neither retinal nor brain atrophy can be shown in patients with isolated unilateral optic neuritis at the time of presentation.

Klaus Kallenbach1, Birgit Sander, Anna Tsakiri, Benedikte Wanscher, Dan Fuglø, Michael Larsen, Henrik Larsson, Jette L Frederiksen.   

Abstract

BACKGROUND: Acute monosymptomatic optic neuritis (ON) may be the earliest manifestation of multiple sclerosis (MS). Atrophy has been shown to be a prominent feature of MS with great impact on disability.
OBJECTIVES: The objectives of this study were to evaluate retinal and brain atrophy and possible associations at the earliest possible stages of MS.
METHODS: In a prospective observational cohort study we included 60 untreated patients with monosymptomatic ON and 19 healthy volunteers. Unaffected fellow eyes were examined with optical coherence tomography (OCT) and normalized brain volumes were calculated based on MRI. Additionally, visual evoked potentials (VEPs) were recorded.
RESULTS: Neither OCT measurements nor brain volume measures revealed signs of localized or generalized atrophy in patients compared with healthy volunteers. Stratification of patients into high risk based on the presence of white matter lesions did not reveal differences. The association between OCT measures and brain volumes previously found could not be confirmed at the time of the first clinical event. VEP latency was significantly prolonged in patients with white matter lesions compared to those without lesions. A trend towards a relationship between VEP amplitude of fellow eyes and brain volumes was noted.
CONCLUSIONS: In this cohort we were not able to show atrophic features in the retina or the brain, and the association between structural measures of the retina and the brain as indicated in the later stages of MS could not be reproduced. These findings suggest that atrophy does require time to evolve and indicate the complexity of the relationship between local and general structural measures.

Entities:  

Mesh:

Year:  2010        PMID: 20847000     DOI: 10.1177/1352458510382017

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  3 in total

1.  Association of Retinal Ganglion Cell Layer Thickness With Future Disease Activity in Patients With Clinically Isolated Syndrome.

Authors:  Hanna G Zimmermann; Benjamin Knier; Timm Oberwahrenbrock; Janina Behrens; Catherina Pfuhl; Lilian Aly; Miriam Kaminski; Muna-Miriam Hoshi; Svenja Specovius; René M Giess; Michael Scheel; Mark Mühlau; Judith Bellmann-Strobl; Klemens Ruprecht; Bernhard Hemmer; Thomas Korn; Friedemann Paul; Alexander U Brandt
Journal:  JAMA Neurol       Date:  2018-09-01       Impact factor: 18.302

2.  Retinal axonal loss begins early in the course of multiple sclerosis and is similar between progressive phenotypes.

Authors:  Jeffrey M Gelfand; Douglas S Goodin; W John Boscardin; Rachel Nolan; Ami Cuneo; Ari J Green
Journal:  PLoS One       Date:  2012-05-23       Impact factor: 3.240

3.  CROP - The Clinico-Radiologico-Ophthalmological Paradox in Multiple Sclerosis: Are Patterns of Retinal and MRI Changes Heterogeneous and Thus Not Predictable?

Authors:  Fahmy Aboulenein-Djamshidian; Martin Krššák; Nermin Serbecic; Helmut Rauschka; Sven Beutelspacher; Ivica Just Kukurová; Ladislav Valkovič; Adnan Khan; Daniela Prayer; Wolfgang Kristoferitsch
Journal:  PLoS One       Date:  2015-11-13       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.