脑电图和多导睡眠图作为抗caspr2脑炎患者长期功能预后的预测指标:一项多中心队列研究

IF 2.7 4区 医学 Q3 CLINICAL NEUROLOGY
Xinbo Zhang, Yuwen Gao, Gengyao Hu, Shuyi Qu, Wenhao Wen, Yanbing Han, Xiaohua Hou, Zaifen Gao, Xiaoli Wang, Chenwei Li, Lei Yang, Xinyu Wen, Kaomin Lin, Junxiang Bao, Yonghong Liu
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引用次数: 0

摘要

目的:自身免疫性脑炎与接触相关蛋白样2 (CASPR2)相关的临床表现不典型,进展缓慢。我们的目的是总结视频脑电图(V-EEG)和视频多导睡眠图(V-PSG)的特征,以实现早期识别和评估长期预后。方法:选取2018-2022年中国四所三级医院抗caspr2脑炎患者27例。所有患者均接受24小时V-EEG监测,其中7例接受额外的夜间V-PSG记录。我们回顾性分析了这些患者的临床和电生理特征、睡眠特征、治疗方法、预后因素和临床结果。采用自身免疫性脑炎临床评估量表(CASE)评估患者的初始严重程度和远期预后。结果:儿童8例,成人19例,其中男性11例,女性16例。其中20例(74.1%)患有罕见的癫痫发作,其中10例首次出现癫痫发作,5例经历癫痫持续状态。除癫痫发作外,一些患者还出现精神症状(14/27)、睡眠障碍(8/27)和Morvan综合征(7/27)。23例(23/27)患者表现出明显的脑电图异常,包括弥漫性慢波活动(DSWA, 7/23)、间歇性慢波活动(12/23)、局灶性/广泛性尖峰间期和尖峰-慢波复合物(7/23)。中位随访时间为40个月(范围:12-78个月)。与正常背景的患者相比,DSWA患者的临床结果更差(CASE≥10,χ2 = 10.188, p = 0.005)。本研究中预后较差的患者表现为睡眠破碎,非快速眼动3期(N3)和快速眼动期(REM)减少。3名患者(3/7)表现出完全缺乏N3睡眠,这与不良预后有关。意义:抗caspr2脑炎患者常观察到累及额叶和颞叶的慢波活动,以及N3和REM睡眠减少。dwa和缺乏N3睡眠可能是抗caspr2脑炎患者预后较差的预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electroencephalography and polysomnography as predictors of long-term functional outcomes in anti-CASPR2 encephalitis: A multicenter cohort study.

Objective: The clinical manifestations of autoimmune encephalitis associated with contactin-associated protein-like 2 (CASPR2) were atypical and progressed slowly. We aimed to summarize the characteristics of video-electroencephalography (V-EEG) and video-polysomnography (V-PSG) to achieve early recognition and assess long-term outcomes.

Methods: 27 patients with anti-CASPR2 encephalitis were enrolled from four tertiary hospitals in China (2018-2022). All patients underwent 24-h V-EEG monitoring, and seven of them received additional overnight V-PSG recording. We retrospectively analyzed the clinical and electrophysiological features, sleep features, treatments, prognostic factors, and clinical outcomes of these patients. The Clinical Assessment Scale in Autoimmune Encephalitis (CASE) was used to assess the initial severity and long-term prognosis.

Results: There were 8 children and 19 adults enrolled, including 11 males and 16 females, respectively. 20 (74.1%) of them suffered from infrequent epileptic seizures, with ten having seizures at initial presentation and five experiencing status epilepticus. In addition to seizures, some developed psychiatric symptoms (14/27), sleep disorders (8/27), and Morvan syndrome (7/27). Twenty-three (23/27) patients presented notable EEG abnormalities, including diffuse slow-wave activities (DSWA, 7/23), intermittent slow-wave activity (12/23), interictal focal/generalized spikes and spike-and-slow-wave complexes (7/23). Median duration of follow-up was 40 months (range: 12-78 months). Compared to those with normal background, patients with DSWA had worse clinical outcomes (CASE ≥10, χ2 = 10.188, p = .005). The patients with poor prognosis in the study showed sleep fragmentation, reduced nonrapid eye movement stage 3 (N3), and rapid eye movement stage (REM). Three patients (3/7) exhibited complete absence of N3 sleep, which was linked to a negative prognosis.

Significance: Slow-wave activities involving the frontal and temporal lobes, as well as reduced N3 and REM sleep, are commonly observed in patients with anti-CASPR2 encephalitis. DSWA and the absence of N3 sleep may serve as predictors of a worse prognosis in anti-CASPR2 encephalitis.

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来源期刊
Epileptic Disorders
Epileptic Disorders 医学-临床神经学
CiteScore
4.10
自引率
8.70%
发文量
138
审稿时长
6-12 weeks
期刊介绍: Epileptic Disorders is the leading forum where all experts and medical studentswho wish to improve their understanding of epilepsy and related disorders can share practical experiences surrounding diagnosis and care, natural history, and management of seizures. Epileptic Disorders is the official E-journal of the International League Against Epilepsy for educational communication. As the journal celebrates its 20th anniversary, it will now be available only as an online version. Its mission is to create educational links between epileptologists and other health professionals in clinical practice and scientists or physicians in research-based institutions. This change is accompanied by an increase in the number of issues per year, from 4 to 6, to ensure regular diffusion of recently published material (high quality Review and Seminar in Epileptology papers; Original Research articles or Case reports of educational value; MultiMedia Teaching Material), to serve the global medical community that cares for those affected by epilepsy.
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