Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Epilepsia. 2021 Feb;62(2):397-407. doi: 10.1111/epi.16807. Epub 2021 Jan 21.
This study aimed to evaluate the proportion of patients with seizures and electroencephalography (EEG) abnormalities in autoimmune encephalitis (AE) and its most common subtypes.
This systematic review followed Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) standards and was registered with the International Prospective Register of Systematic Reviews (PROSPERO). We searched Medline All, Embase, and PsychINFO in Ovid from inception to June 2019 for articles pertaining to AE and seizure. Included studies reported seizure and/or EEG data in cohorts of ≥10 AE patients. Patient demographics, antibody type, seizure incidence, and EEG findings were extracted. Review of studies and data extraction were performed in duplicate. In addition to descriptive analysis, quantitative synthesis stratified by autoantibody subtype was performed with logistic regression and chi-square analyses.
Our search yielded 3856 abstracts: 1616 were selected for full-text review and 118 studies met eligibility criteria. Of 3722 antibody-positive AE patients, 2601 (69.9%) had clinical seizures during the course of their illness. Of the 2025 patients with antibody-positive AE and available EEG data, 1718 (84.8%) had some EEG abnormality (eg, epileptiform discharges, slowing, and so on). Anti- N-methyl-d-aspartate (NMDA) receptor encephalitis (anti-NMDARE) was the most commonly reported type of AE (1985/3722, 53.3%). Of the anti-NMDARE patients with available seizure or EEG data, 71.8% (n = 1425/1985) had clinical seizures during their illness, and 89.7% (n = 1172/1306) had EEG abnormalities. For all AE patients and in the anti-NMDARE subpopulation, seizures were more common in younger patients (p < .05).
This systematic review provides an estimate of the proportion of AE patients with seizures, confirming the magnitude of seizure burden in this population. Prospective studies are needed to understand population-based prevalence of seizures, identify factors associated with seizures, and evaluate particular EEG findings as biomarkers of seizures and outcomes in AE.
本研究旨在评估自身免疫性脑炎(AE)及其最常见亚型患者中癫痫发作和脑电图(EEG)异常的比例。
本系统评价遵循系统评价和荟萃分析的首选报告项目(PRISMA)标准,并在国际前瞻性系统评价注册库(PROSPERO)中进行了注册。我们从成立开始在 Ovid 旗下的 Medline All、Embase 和 PsychINFO 中进行了系统性检索,以获取与 AE 和癫痫发作相关的文章。纳入的研究报告了≥10 例 AE 患者队列中的癫痫发作和/或 EEG 数据。提取患者人口统计学、抗体类型、癫痫发作发生率和 EEG 结果。对研究和数据提取进行了双重审查。除了描述性分析外,还使用逻辑回归和卡方分析对自身抗体亚型进行了分层定量综合分析。
我们的搜索产生了 3856 篇摘要:其中 1616 篇被选入全文审查,118 篇研究符合入选标准。在 3722 例抗体阳性 AE 患者中,2601 例(69.9%)在疾病过程中出现临床癫痫发作。在 2025 例有抗体阳性 AE 和可用 EEG 数据的患者中,1718 例(84.8%)存在某种 EEG 异常(如癫痫样放电、减慢等)。抗 N-甲基-D-天冬氨酸(NMDA)受体脑炎(抗-NMDARE)是最常报告的 AE 类型(1985/3722,53.3%)。在有癫痫发作或 EEG 数据的抗-NMDARE 患者中,71.8%(n=1425/1985)在发病期间出现临床癫痫发作,89.7%(n=1172/1306)出现 EEG 异常。对于所有 AE 患者和抗-NMDARE 患者亚群,癫痫发作在年轻患者中更为常见(p<.05)。
本系统评价提供了 AE 患者癫痫发作比例的估计值,证实了该人群中癫痫发作负担的严重程度。需要前瞻性研究来了解癫痫发作的人群患病率,确定与癫痫发作相关的因素,并评估特定的 EEG 发现作为 AE 中癫痫发作和结局的生物标志物。