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Invest. Ophthalmol. Vis. Sci. · May 2014
Latency of multifocal visual evoked potentials in nonoptic neuritis eyes of multiple sclerosis patients associated with optic radiation lesions.
- Daniah Alshowaeir, Con Yiannikas, Raymond Garrick, John Parratt, Michael H Barnett, Stuart L Graham, and Alexander Klistorner.
- Department of Ophthalmology, University of Sydney, Sydney, Australia Department of Ophthalmology, King Saud University, Riyadh, Saudi Arabia.
- Invest. Ophthalmol. Vis. Sci. 2014 May 15; 55 (6): 3758-64.
PurposeThe aim of the study was to test the hypothesis that latency delay of multifocal visual evoked potentials (mfVEP) in nonoptic neuritis (NON) eyes of multiple sclerosis (MS) patients is related to retrochiasmal demyelinating lesions.MethodsA total of 57 MS patients with no history of optic neuritis at least in one eye, and 25 age- and sex-matched healthy controls was enrolled. Probabilistic tractography was used to reconstruct optic radiation (OR) fibers. The MS lesion volume within and outside of OR was calculated. Diffusion tensor imaging (DTI) indices were measured along OR fibers. The relationship of the mfVEP latency with OR lesions and DTI indices was examined.ResultsAverage mfVEP latency in the MS cohort was significantly delayed compared to controls (P < 0.0001). Of the patients, 77% demonstrated OR lesions. Axial, radial, and mean diffusivity were significantly abnormal in MS patients (P < 0.001). Partial correlation demonstrated significant association between mfVEP latency delay and OR lesion load. There was also significant correlation between MfVEP latency and OR DTI. Subgroup analysis revealed significantly higher correlations in patients without a history of ON in either eye compared to the fellow eye of patients with previous ON.ConclusionsThe findings of this study support our hypothesis that latency delay of the mfVEP in eyes of MS patients without previous ON is related to retrogenicular demyelinating lesions. Additionally, this study demonstrated that a previous episode of ON in the fellow eye may be a significant confounding factor, masking the relationship between the latency and OR lesions.Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.
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