Thurtell M J, Bala E, Yaniglos S S, Rucker J C, Peachey N S, Leigh R J
Departments of Neurology, University Hospitals Case Medical Center, Cleveland, USA.
Neurology. 2009 Dec 1;73(22):1849-57. doi: 10.1212/WNL.0b013e3181c3fd43.
Contrast acuity (identification of low-contrast letters on a white background) is frequently reduced in patients with demyelinating optic neuropathy associated with multiple sclerosis (MS), even when high-contrast (Snellen) visual acuity is normal. Since visual evoked potentials (VEPs) induced with high-contrast pattern-reversal stimuli are typically increased in latency in demyelinating optic neuropathy, we asked if VEPs induced with low-contrast stimuli would be more prolonged and thus helpful in identifying demyelinating optic neuropathy in MS.
We studied 15 patients with clinically definite MS and 15 age-matched normal controls. All subjects underwent a neuro-ophthalmologic assessment, including measurement of high-contrast visual acuity and low-contrast acuities with 25%, 10%, 5%, 2.5%, and 1.25% contrast Sloan charts. In patients with MS, peripapillary retinal nerve fiber layer (RNFL) thickness was determined using optical coherence tomography. Monocular VEPs were induced using pattern-reversal checkerboard stimuli with 100% and 10% contrast between checks, at 5 spatial frequencies (8-130 minutes of arc).
VEP latencies were significantly increased in response to low- compared with high-contrast stimuli in both groups. VEP latencies were significantly greater in patients with MS than controls for both high- and low-contrast stimuli. VEP latencies correlated with high- and low-contrast visual acuities and RNFL thickness. VEPs were less likely to be induced with low- than with high-contrast stimuli in eyes with severe residual visual loss.
Visual evoked potentials obtained in patients with multiple sclerosis using low-contrast stimuli are increased in latency or absent when compared with those obtained using high-contrast stimuli and, thus, may prove to be helpful in identifying demyelinating optic neuropathy.
与多发性硬化症(MS)相关的脱髓鞘性视神经病变患者,即使高对比度(斯内伦)视力正常,其对比敏感度(在白色背景上识别低对比度字母)也常降低。由于高对比度模式翻转刺激诱发的视觉诱发电位(VEP)在脱髓鞘性视神经病变中潜伏期通常延长,我们想知道低对比度刺激诱发的VEP是否会延长更多,从而有助于识别MS中的脱髓鞘性视神经病变。
我们研究了15例临床确诊的MS患者和15例年龄匹配的正常对照者。所有受试者均接受了神经眼科评估,包括使用25%、10%、5%、2.5%和1.25%对比度的斯隆图表测量高对比度视力和低对比度视力。对于MS患者,使用光学相干断层扫描测定视乳头周围视网膜神经纤维层(RNFL)厚度。使用方格之间对比度为100%和10%的模式翻转棋盘格刺激,在5个空间频率(8 - 130分视角)下诱发单眼VEP。
两组中,与高对比度刺激相比,低对比度刺激诱发的VEP潜伏期均显著延长。对于高对比度和低对比度刺激,MS患者的VEP潜伏期均显著长于对照组。VEP潜伏期与高对比度和低对比度视力以及RNFL厚度相关。在严重残余视力丧失的眼中,低对比度刺激比高对比度刺激诱发VEP的可能性更小。
与使用高对比度刺激获得的结果相比,MS患者使用低对比度刺激获得的视觉诱发电位潜伏期延长或缺失,因此可能有助于识别脱髓鞘性视神经病变。