Reconsideration of conversion to multiple sclerosis: one-year cerebral lesion appearance rate of Japanese aquaporin-4 antibody-negative optic neuritis patients.

IF 2.1 3区 医学 Q2 OPHTHALMOLOGY
Satoshi Ueki, Yukari Hasegawa, Tetsuhisa Hatase, Izumi Kawachi, Takeo Fukuchi
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引用次数: 0

Abstract

Purpose: To analyze the rate of new cerebral lesions' appearance within 6-12 months in Japanese optic neuritis patients who at onset had no cerebral lesions suggestive of multiple sclerosis (MS) and were negative for aquaporin-4 (AQP4) antibodies.

Study design: Retrospective study.

Methods: Medical records of 66 adult patients with optic neuritis were reviewed. Patients positive for AQP4, myelin oligodendrocyte glycoprotein, or antinuclear antibodies were excluded. Those without cerebral lesions on initial magnetic resonance imaging (MRI) underwent follow-up MRI within 6-12 months. Clinical characteristics and subsequent neurological diagnoses were analyzed.

Results: Forty-seven patients met the inclusion criteria (mean age, 41.9±16.7 years; 13 men, 34 women). Forty-two cases were unilateral, five bilateral; 19 had disc swelling, and 28 did not. The mean worst logMAR was 1.13±0.96. Two patients experienced recurrence within 1 year. Of the 27 patients without initial cerebral lesions, 20 underwent follow-up MRI; 3 (15%) developed new lesions. These three were later diagnosed as two MS and one suspected MS cases.

Conclusion: Follow-up MRI within 6-12 months revealed new cerebral lesions in 15% of patients, with 10% diagnosed with MS. This highlights the importance of follow-up imaging even in AQP4 antibody-negative optic neuritis patients without initial cerebral lesions, especially in the absence of other diseases like neuromyelitis optica spectrum disorders.

日本水通道蛋白-4抗体阴性视神经炎患者一年内脑损伤出现率的研究
目的:分析日本视神经炎患者发病时无提示多发性硬化症(MS)的脑病变,且AQP4抗体阴性的6-12个月内新发脑病变的发生率。研究设计:回顾性研究。方法:回顾性分析66例视神经炎患者的临床资料。排除AQP4、髓鞘少突胶质细胞糖蛋白或抗核抗体阳性的患者。首次磁共振成像(MRI)无脑病变者在6-12个月内随访MRI。分析临床特点和随后的神经学诊断。结果:47例患者符合纳入标准(平均年龄41.9±16.7岁;男性13人,女性34人)。单侧42例,双侧5例;19例有椎间盘肿胀,28例无。平均最差logMAR为1.13±0.96。2例患者1年内复发。在27例没有初始脑病变的患者中,20例接受了后续MRI检查;3例(15%)出现新的病变。这三人后来被诊断为2例多发性硬化症和1例疑似多发性硬化症。结论:6-12个月内随访MRI发现15%的患者出现新的脑病变,其中10%诊断为ms。这突出了随访成像的重要性,即使是AQP4抗体阴性的视神经炎患者没有初始脑病变,特别是在没有其他疾病如视神经脊髓炎谱系障碍的情况下。
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来源期刊
CiteScore
4.80
自引率
8.30%
发文量
65
审稿时长
6-12 weeks
期刊介绍: The Japanese Journal of Ophthalmology (JJO) was inaugurated in 1957 as a quarterly journal published in English by the Ophthalmology Department of the University of Tokyo, with the aim of disseminating the achievements of Japanese ophthalmologists worldwide. JJO remains the only Japanese ophthalmology journal published in English. In 1997, the Japanese Ophthalmological Society assumed the responsibility for publishing the Japanese Journal of Ophthalmology as its official English-language publication. Currently the journal is published bimonthly and accepts papers from authors worldwide. JJO has become an international interdisciplinary forum for the publication of basic science and clinical research papers.
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