Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (7)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Caruana, P. A.
Right arrow Articles by Hawkins, C. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Caruana, P. A.
Right arrow Articles by Hawkins, C. P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 123, No. 7, 1471-1480, July 2000
© 2000 Oxford University Press

Correlation of MRI lesions with visual psychophysical deficit in secondary progressive multiple sclerosis

P. A. Caruana1,2, M. B. Davies1,2, S. J. M. Weatherby1,2, R. Williams3, N. Haq3, D. H. Foster4,5 and C. P. Hawkins1,2

Keele Multiple Sclerosis Research Group: 1 Department of Neurology, Royal Infirmary, 2 Keele University School of Post-Graduate Medicine, 3 Cornwall House Magnetic Resonance Imaging Centre and 4 Department of Communication and Neuroscience, Keele University, Stoke-on-Trent and 5 Visual and Computational Neuroscience Group, Department of Optometry and Neuroscience, University of Manchester Institute of Science and Technology, Manchester, UK

Correspondence to: Dr Brendan Davies, Department of Neurology, North Staffs Royal Infirmary, Princes Road, Stoke-on-Trent ST4 7LN, UK E-mail: Brendand{at}mcmail.com

The aim of this work was, first, to clarify the nature of the relationship between the sensory deficit in the demyelinated visual pathway and morphological changes revealed by MRI and, secondly, to test whether there was a preferential effect of demyelination for either the magnocellular or parvocellular pathway in established multiple sclerosis. Twenty-four patients with secondary progressive multiple sclerosis were studied psychophysically and by MRI of the optic nerve and brain. MRI was performed with a Phillips (0.5T) scanner. Visual pathway MRI lesion load was evaluated independently using the total optic nerve lesion length and lesion area seen on STIR (short inversion time inversion recovery) images of the optic nerve and the total post-chiasmal lesion area on T1-, T2- and proton-density-weighted images of the brain. Psychophysical tests determined 75%-seeing thresholds for horizontal gratings consisting of isoluminant red and green sinusoids of the same spatial frequency combined out-of-phase for preferential stimulation of the parvocellular system and in-phase for preferential stimulation of the magnocellular system. It was found that, in this group of patients, visual psychophysical loss was significantly correlated with lesion area seen on proton density MRI sequences of the post-chiasmal visual pathway, and that the parvocellular pathway was more affected than the magnocellular pathway, especially at lower spatial frequencies.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mult SclerHome page
L N Brown, L M Metz, and M Eliasziw
Identifying reliable change in tactile temporal thresholds in multiple sclerosis: test-retest reliability
Multiple Sclerosis, September 1, 2006; 12(5): 573 - 577.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.