Abstract

ObjectiveThis single-center study was conducted in a cohort of patients with anti-LGI1 encephalitis to investigate the factors related to their functional recovery.MethodsWe retrospectively collected the clinical information of patients admitted to Xuanwu Hospital from January 2014 until December 2019, and followed up for at least 12 months.ResultsA total of 67 patients were included, and 57 completed the 12-month follow-up. Most of the patients (55/57, 96.5%) achieved functional improvement after immunotherapy, and 26 (45.6%) became symptom-free. Compared to patients with complete recovery, patients with partial or no recovery had significantly higher incidences of consciousness disorders (25.8% vs. 0%, P<0.05) and positive LGI1 antibodies in cerebrospinal fluid (CSF) (71.0% vs. 46.2%, P<0.05). These patients also had a lower Barthel Index both upon admission and at discharge, as well as a higher incidence of relapse (25.8% vs. 3.8%; P<0.05 each). Univariate logistic regression showed that positive LGI1 antibodies in CSF and relapse were associated with incomplete recovery at 1-year follow-up (both P<0.05), but only relapse remained statistically significant after multivariate logistic regression (P=0.034).ConclusionPatients with LGI1 antibodies in CSF and those who relapsed were more likely to experience worse outcome. Early recognition of these patients, combined with more aggressive immunotherapy may result in better recovery.

Highlights

  • Anti-LGI1 encephalitis is a newly discovered autoimmune encephalitis and a relatively common cause of limbic encephalitis [1]

  • We retrospectively identified patients with definite anti-LGI1 encephalitis admitted to the Department of Neurology of Xuanwu Hospital, Capital Medical University, between January 2014 and December 2019 (Supplemental Figure 1)

  • Relapse was defined as clinical worsening during treatment after initial improvement that required a change of medication, or clinical worsening observed after recovery and being off-medication

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Summary

Introduction

Anti-LGI1 (leucine-rich glioma-inactivated 1) encephalitis is a newly discovered autoimmune encephalitis and a relatively common cause of limbic encephalitis [1]. Recent publications reported the key symptoms of anti-LGI1 encephalitis patients, including subacute cognitive decline and seizures ( faciobrachial dystonic seizures), as well as a good response to immunotherapy [1,2,3,4,5]. Long-term outcome has been described in some studies [2,3,4,5], but little is known about the potential risk factors of unfavorable outcome or relapse. This study aimed to explore these factors

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