The use of optical coherence tomography and visual evoked potentials in the 2024 McDonald diagnostic criteria for multiple sclerosis

Shiv Saidha, Ari J Green, Letizia Leocani, Angela Vidal-Jordana, Rachel C Kenney, Gabriel Bsteh, Olivier Outteryck, Alan Thompson, Xavier Montalban, Timothy Coetzee, Axel Petzold, Friedemann Paul, Laura J Balcer, Peter A Calabresi
{"title":"The use of optical coherence tomography and visual evoked potentials in the 2024 McDonald diagnostic criteria for multiple sclerosis","authors":"Shiv Saidha, Ari J Green, Letizia Leocani, Angela Vidal-Jordana, Rachel C Kenney, Gabriel Bsteh, Olivier Outteryck, Alan Thompson, Xavier Montalban, Timothy Coetzee, Axel Petzold, Friedemann Paul, Laura J Balcer, Peter A Calabresi","doi":"10.1016/s1474-4422(25)00275-3","DOIUrl":null,"url":null,"abstract":"The 2024 revisions of the McDonald diagnostic criteria include the optic nerve as a fifth anatomical location within the CNS for the diagnosis of multiple sclerosis, in addition to periventricular, juxtacortical or cortical, infratentorial, and spinal cord lesions. Demonstration of dissemination in space can now be achieved with the detection of typical lesions in at least two of these five locations. We review the evidence supporting the use of optical coherence tomography (OCT) and visual evoked potentials (VEPs) to show optic nerve involvement in the diagnosis of multiple sclerosis. We also report consensus recommendations for their use. Provided there is no better explanation for optic nerve involvement and that rigorous quality control is applied, OCT-derived peripapillary retinal nerve fibre layer inter-eye differences of 6 μm or greater or composite macular ganglion cell and inner plexiform layer inter-eye differences of 4 μm or greater support optic nerve injury. Delayed VEP latency, which depends on technical and methodological factors, and is centre and device dependent, supports demyelinating optic nerve injury when done with appropriate technical knowledge and interpretation.","PeriodicalId":22676,"journal":{"name":"The Lancet Neurology","volume":"36 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Lancet Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/s1474-4422(25)00275-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The 2024 revisions of the McDonald diagnostic criteria include the optic nerve as a fifth anatomical location within the CNS for the diagnosis of multiple sclerosis, in addition to periventricular, juxtacortical or cortical, infratentorial, and spinal cord lesions. Demonstration of dissemination in space can now be achieved with the detection of typical lesions in at least two of these five locations. We review the evidence supporting the use of optical coherence tomography (OCT) and visual evoked potentials (VEPs) to show optic nerve involvement in the diagnosis of multiple sclerosis. We also report consensus recommendations for their use. Provided there is no better explanation for optic nerve involvement and that rigorous quality control is applied, OCT-derived peripapillary retinal nerve fibre layer inter-eye differences of 6 μm or greater or composite macular ganglion cell and inner plexiform layer inter-eye differences of 4 μm or greater support optic nerve injury. Delayed VEP latency, which depends on technical and methodological factors, and is centre and device dependent, supports demyelinating optic nerve injury when done with appropriate technical knowledge and interpretation.
光学相干断层扫描和视觉诱发电位在多发性硬化症2024麦克唐纳诊断标准中的应用
2024年修订的McDonald诊断标准将视神经作为多发性硬化症在中枢神经系统中的第五个解剖位置,除了脑室周围、皮质或皮质旁、幕下和脊髓病变。通过在这五个地点中的至少两个地点检测到典型病变,现在可以实现空间传播的演示。我们回顾了支持使用光学相干断层扫描(OCT)和视觉诱发电位(VEPs)来显示视神经受累在多发性硬化症诊断中的证据。我们还报告了对其使用的一致建议。如果对视神经受累没有更好的解释,并有严格的质量控制,oct源性乳头周围视网膜神经纤维层眼间差异6 μm及以上或复合黄斑神经节细胞与内丛状层眼间差异4 μm及以上支持视神经损伤。VEP延迟潜伏期取决于技术和方法因素,并且依赖于中心和设备,在适当的技术知识和解释下,支持脱髓鞘视神经损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信