University of Michigan Department of Neurology, 1500 E Medical Center Dr # 1914, Ann Arbor, MI 48109, United States; University of Cincinnati College of Medicine, Department of Neurology and Rehabilitation Medicine, Stetson Building Suite 2300, 260 Stetson St., Cincinnati, OH 45267, United States.
University of Michigan Department of Neurology, 1500 E Medical Center Dr # 1914, Ann Arbor, MI 48109, United States; University of Colorado School of Medicine, Department of Neurology, 13001 E 17th Pl, Aurora, CO 80045, United States.
Seizure. 2024 Feb;115:44-49. doi: 10.1016/j.seizure.2023.12.020. Epub 2023 Dec 27.
The prevalence of epilepsy in patients with multiple sclerosis (MS) is three to six times the prevalence in the general population. Mechanisms resulting in increased seizure risk are not fully understood. Our objective is to characterize patients with MS and epilepsy regarding timing of diagnoses, MS and seizure (SZ) type, EEG findings suggesting cortical dysfunction, frequency of status epilepticus (SE), and seizure freedom.
This was a single center retrospective study. Cases were obtained via DataDirect via the University of Michigan electronic medical record from January 1, 2006 through October, 12, 2016. The University of Michigan Health System is a large academic institute with a tertiary referral center and an Autoimmunity Center of Excellence. Patients were included if chart listed one or more of the top 62 epilepsy, and one or more of the top 2 MS, most frequently entered ICD9 and ICD10 codes. Patients with alternative epilepsy etiology were excluded. 74 of 361 patients were included. We collected information regarding demographics, MS and SZ type, age at diagnosis, imaging, EEG, seizure freedom, medications, and SE.
We found a high percentage of patients with SE. Most patients with imaging had multiple lesions at seizure onset. 27/54 of patients with EEG data showed electrographic evidence of cortical dysfunction. 6/8 of EEGs in PPMS showed features consistent with cortical dysfunction, followed by 9/17 in SPMS and 11/23 in RRMS. 7/8 of patients with PPMS showed EEG evidence of temporal lobe dysfunction.
Time of seizure onset relative to MS diagnosis varied with MS type suggesting distinct pathophysiology. EEG results correspond with reports of increased cortical damage and temporal dysfunction in PPMS, but are unique as a functional modality (EEG) as indicator of gray matter dysfunction. EEG findings differed in RRMS and progressive MS suggesting possibility of supportive diagnostic marker. Our data suggests higher risk of SE in progressive MS and diminished rate of seizure freedom for MS patients with SE. We conclude that early treatment with antiseizure medication would be beneficial for MS patients with SE and with progressive MS forms and SZ, in agreement with previous studies.
多发性硬化症 (MS) 患者的癫痫患病率是普通人群的三到六倍。导致癫痫发作风险增加的机制尚未完全阐明。我们的目标是描述 MS 和癫痫患者的诊断时间、MS 和癫痫 (SZ) 类型、提示皮质功能障碍的脑电图发现、癫痫持续状态 (SE) 的频率以及无癫痫发作。
这是一项单中心回顾性研究。病例通过密歇根大学电子病历中的 DataDirect 从 2006 年 1 月 1 日至 2016 年 10 月 12 日获得。密歇根大学健康系统是一家大型学术机构,拥有三级转诊中心和自身免疫卓越中心。如果图表列出了一个或多个前 62 种癫痫和一个或多个前 2 种 MS,则将患者纳入研究,最常输入 ICD9 和 ICD10 代码。排除有其他癫痫病因的患者。361 名患者中有 74 名符合条件。我们收集了有关人口统计学、MS 和 SZ 类型、诊断时的年龄、影像学、脑电图、无癫痫发作、药物和 SE 的信息。
我们发现癫痫持续状态的患者比例很高。大多数有影像学检查的患者在癫痫发作时都有多个病变。有脑电图数据的 54 名患者中有 27 名显示出皮质功能障碍的脑电图证据。8 名进展型多发性硬化症患者中有 6 名脑电图显示皮质功能障碍特征,随后在继发进展型多发性硬化症患者中有 11 名和复发缓解型多发性硬化症患者中有 9 名。8 名进展型多发性硬化症患者中有 7 名脑电图显示颞叶功能障碍。
癫痫发作的时间与 MS 诊断的关系因 MS 类型而异,表明存在不同的病理生理学机制。脑电图结果与 PPMS 中皮质损伤和颞叶功能障碍增加的报告相符,但作为指示灰质功能障碍的功能模式 (脑电图) 是独特的。复发缓解型多发性硬化症和进行性多发性硬化症的脑电图结果不同,提示可能存在支持性诊断标志物。我们的数据表明,进行性 MS 和有 SE 的 MS 患者的 SE 风险更高,且有 SE 的 MS 患者的癫痫无发作率更低。我们得出的结论是,与之前的研究一致,早期使用抗癫痫药物治疗对有 SE 和进行性 MS 形式和 SZ 的 MS 患者有益。