Neuroplasticity predicts outcome of optic neuritis independent of tissue damage

视神经炎 医学 磁共振成像 功能磁共振成像 视神经 神经可塑性 神经科学 多发性硬化 听力学 眼科 心理学 放射科 精神科
作者
Thomas M. Jenkins,Ahmed Toosy,Olga Ciccarelli,Katherine Miszkiel,Claudia A. M. Gandini Wheeler‐Kingshott,Andrew Henderson,Constantinos Kallis,Laura Mancini,Gordon T. Plant,David H. Miller,Alan J. Thompson
出处
期刊:Annals of Neurology [Wiley]
卷期号:67 (1): 99-113 被引量:82
标识
DOI:10.1002/ana.21823
摘要

Abstract Objectives To determine whether lateral occipital complex (LOC) activation with functional magnetic resonance imaging (fMRI) predicts visual outcome after clinically isolated optic neuritis (ON). To investigate the reasons behind good recovery following ON, despite residual optic nerve demyelination and neuroaxonal damage. Methods Patients with acute ON and healthy volunteers were studied longitudinally over 12 months. Structural MRI, visual evoked potentials (VEPs), and optical coherence tomography (OCT) were used to quantify acute inflammation, demyelination, conduction block, and later to estimate remyelination and neuroaxonal loss over the entire visual pathway. The role of neuroplasticity was investigated using fMRI. Multivariable linear regression analysis was used to study associations between vision, structure, and function. Results Greater baseline fMRI responses in the LOCs were associated with better visual outcome at 12 months. This was evident on stimulation of either eye ( p = 0.007 affected; p = 0.020 fellow eye), and was independent of measures of demyelination and neuroaxonal loss. A negative fMRI response in the LOCs at baseline was associated with a relatively worse visual outcome. No acute electrophysiological or structural measures, in the anterior or posterior visual pathways, were associated with visual outcome. Interpretation Early neuroplasticity in higher visual areas appears to be an important determinant of recovery from ON, independent of tissue damage in the anterior or posterior visual pathway, including neuroaxonal loss (as measured by MRI, VEP, and OCT) and demyelination (as measured by VEP). ANN NEUROL 2010;67:99–113

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