Review of the Longitudinal Management of Autoimmune Encephalitis, Potential Biomarkers, and Novel Therapeutics.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2024-08-01 Epub Date: 2024-05-29 DOI:10.1212/CPJ.0000000000200306
Ahmad Z Mahadeen, Alise K Carlson, Jeffrey A Cohen, Rachel Galioto, Justin R Abbatemarco, Amy Kunchok
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Abstract

Purpose of review: Increasing awareness and earlier diagnosis of autoimmune encephalitis (AE) have led to a greater number of patients being cared for longitudinally by neurologists. Although many neurologists are now familiar with the general approach to diagnosis and acute immunosuppression, this review aims to provide neurologists with guidance related to management beyond the acute phase of disease, including long-term immunosuppression, monitoring, potential biomarkers of disease activity, outcome measures, and symptom management.

Recent findings: Observational studies in AE have demonstrated that early diagnosis and treatment is associated with improved neurologic outcomes, particularly in AE with antibodies targeting neuronal cell surface/synaptic proteins. The literature regarding long-term management is evolving. In addition to traditional immunosuppressive approaches, there is emerging use of novel immunosuppressive therapies (ISTs) in case series, and several randomized controlled trials are planned. Novel biomarkers of disease activity and methods to measure outcomes and response to treatment are being explored. Furthermore, it is increasingly recognized that many individuals have chronic symptoms affecting quality of life including seizures, cognitive impairment, fatigue, sleep disorders, and mood disorders, and there are emerging data supporting the use of patient centered outcome measures and multidisciplinary symptom-based care.

Summary: This review aims to summarize recent literature and offer a practical approach to long-term management of adult patients with AE through a multidisciplinary approach. We summarize current knowledge on ISTs, potential biomarkers of disease activity, outcome measures, and long-term sequelae. Further research is needed to answer questions regarding optimal IST, biomarker validity, and sequelae of disease.

回顾自身免疫性脑炎的纵向管理、潜在生物标记物和新疗法。
综述目的:随着对自身免疫性脑炎(AE)认识的提高和诊断的提早,越来越多的患者接受了神经科医生的纵向治疗。尽管许多神经科医生现在已经熟悉了诊断和急性免疫抑制的一般方法,但本综述旨在为神经科医生提供有关疾病急性期后管理的指导,包括长期免疫抑制、监测、疾病活动的潜在生物标志物、结果测量和症状管理:最近的研究结果:对AE的观察性研究表明,早期诊断和治疗与神经系统预后的改善有关,尤其是针对神经细胞表面/突触蛋白抗体的AE。有关长期治疗的文献也在不断发展。除了传统的免疫抑制方法外,新型免疫抑制疗法(ISTs)也开始在系列病例中使用,并计划开展多项随机对照试验。目前正在探索疾病活动的新型生物标志物以及衡量疗效和治疗反应的方法。此外,越来越多的人认识到,许多人都有影响生活质量的慢性症状,包括癫痫发作、认知障碍、疲劳、睡眠障碍和情绪障碍,而且新出现的数据支持使用以患者为中心的结果测量方法和基于症状的多学科护理。摘要:本综述旨在总结最新文献,并通过多学科方法为成人 AE 患者的长期管理提供实用方法。我们总结了目前有关 IST、疾病活动的潜在生物标志物、结果测量和长期后遗症的知识。要回答有关最佳 IST、生物标志物有效性和疾病后遗症的问题,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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