Multifocal visual evoked potential evaluation for diagnosis of acute optic neuritis and for prediction of visual outcome and ganglion cell layer thinning following optic neuritis

被引:7
作者
Pihl-Jensen, Gorm [1 ,2 ,3 ]
Wanscher, Benedikte [4 ]
Frederiksen, Jette Lautrup [1 ,2 ,3 ]
机构
[1] Rigshosp Glostrup, Dept Neurol, Clin Opt Neuritis, Valdemar Hansens Vej 13, DK-2600 Glostrup, Denmark
[2] Rigshosp Glostrup, Dept Neurol, Clin Multiple Sclerosis, Valdemar Hansens Vej 13, DK-2600 Glostrup, Denmark
[3] Univ Copenhagen, Copenhagen, Denmark
[4] Rigshosp Glostrup, Dept Clin Neurophysiol, Glostrup, Denmark
关键词
Optic neuritis; multifocal visual evoked potentials; optical coherence tomography; neuroaxonal loss; MULTIPLE-SCLEROSIS; COHERENCE TOMOGRAPHY; AXONAL LOSS; SEGMENTATION; DYSFUNCTION; PERIMETRY; PATHWAY; DAMAGE;
D O I
10.1177/1352458520975732
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background:: While damage to the optic nerve following optic neuritis (ON) is readily quantifiable, the evaluation of prognosis for visual function and neuroaxonal loss in the acute ON is challenging. Objective:: The objective of this study is to investigate the value of multifocal visual evoked potential (mfVEP) in acute ON, diagnostically for acute ON and prognostically for visual outcome and subsequent ganglion cell/inner plexiform layer thickness (GCLIPLt). Methods:: A prospective cohort study of mfVEP and full-field visual evoked potential (ffVEP) in acute, unilateral ON (onset < 31 days) was conducted. Comparisons with healthy controls (n = 30) and association analysis with follow-up optical coherence tomography (OCT) measurements (of the GCLIPLt) and visual function (Sloan low-contrast visual acuity (LCVA)) were conducted. Results:: Seventy-nine ON patients were included (mean: 17 days from onset). Excluding measurements with conduction block, ffVEP (n = 54) and mfVEP (n = 44) showed sensitivities of 89% and 84% to a specificity of 97%. 65/79 patients were re-examined (mean: 200 days follow-up). mfVEP amplitude and latency inter-eye asymmetry in acute ON correlated with GCLIPLt (r = 0.587 and Spearman's rho = 0.597, for both, p < 0.001). mfVEP amplitude correlated with LCVA inter-eye asymmetry at follow-up (r = 0.421, p < 0.001), mfVEP latency did not. Conclusion: mfVEP may support the prognostic evaluation of acute ON patients and prove valuable in future neuroprotective and remyelinating trials. In acute ON, the increase in diagnostic value of mfVEP to ffVEP may be limited due to widespread conduction block.
引用
收藏
页码:1717 / 1726
页数:10
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