Abstract

Objectives: Autonomic dysfunction is a common symptom of anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis; however, it has been poorly researched. The purpose of this study was to compare the clinical features, tumor occurrence, intensive care unit (ICU) admission, mechanical ventilation, imaging assessment, cerebrospinal fluid examination, disease severity, and immunotherapy in patients with anti-NMDAR encephalitis with or without autonomic dysfunction.Methods: A retrospective study of anti-NMDAR encephalitis patients diagnosed between January 2016 and April 2020 was performed at the First Affiliated Hospital of Zhengzhou University. Patients were divided into two groups according to whether they had autonomic dysfunction, and their clinical features, treatment, and prognosis were compared.Results: A total of 119 patients with anti-NMDAR encephalitis were included in this study. Seventy-three patients (61.3%) had autonomic dysfunction, while the remaining 46 (38.7%) did not. Sinus tachycardia (69.9%) was the autonomic dysfunction with the highest incidence, while the incidences of symptoms including constipation, central hypopnea, and others gradually decreased. Compared to the group without autonomic dysfunction, the prevalence of the main clinical symptoms such as epileptic seizure (P = 0.003), involuntary movement (P = 0.028), and decreased consciousness (P < 0.001) were higher in the group with autonomic dysfunction, which also more frequently presented with complications such as pulmonary infection (P < 0.001) and abnormal liver function (P = 0.001). Moreover, the rates of ICU admission (P < 0.001) and mechanical ventilation (P = 0.001), as well as the modified Rankin scale (mRS) scores at admission (P < 0.001), maximum mRS scores during the course of disease (P < 0.001), and mRS scores at discharge (P < 0.001) were higher in the patients with autonomic dysfunction than in those without. The number of patients in the autonomic dysfunction group who underwent ≥2 immunotherapies was also higher than that in the group without autonomic dysfunction (P < 0.001).Conclusion: Sinus tachycardia is the most common type of autonomic dysfunction in anti-NMDAR encephalitis. Compared to patients without autonomic dysfunction, those with autonomic dysfunction had a higher incidence of epilepsy, involuntary movements, decreased consciousness, pulmonary infections, abnormal liver function, ICU admissions, and mechanical ventilation; moreover, the severity of the disease was greater, and their prognosis worse. Therefore, such patients require intensive immunotherapy.

Highlights

  • Autoimmune encephalitis (AE) refers to a non-infectious encephalitis that is mediated by autoimmune mechanisms

  • This study aimed to explore the effects of autonomic dysfunction on clinical features, imaging and laboratory examination, disease severity, and treatment in patients with anti-NMDAR encephalitis to provide a future reference for the diagnosis and treatment of anti-NMDAR encephalitis

  • A total of 119 patients with a definitive diagnosis of anti-NMDAR encephalitis were included in this study

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Summary

Introduction

Autoimmune encephalitis (AE) refers to a non-infectious encephalitis that is mediated by autoimmune mechanisms. AntiN-methyl-D-aspartate receptor (NMDAR) encephalitis is the most common AE [1]. Its pathogenic mechanism is based on in vivo binding of anti-NMDAR antibodies to the extracellular NR1 subunit of the NMDAR, thereby disrupting the normal excitatory transmission in glutamatergic neurons and causing neuronal damage by inhibiting the localization and accumulation of NMDAR on neuronal cell membranes [2]. Autonomic dysfunction is a common clinical symptom of anti-NMDAR encephalitis; at present, there are few studies and with conflicting results, which explore its effects on patients’ condition and prognosis [4,5,6]. This study aimed to explore the effects of autonomic dysfunction on clinical features, imaging and laboratory examination, disease severity, and treatment in patients with anti-NMDAR encephalitis to provide a future reference for the diagnosis and treatment of anti-NMDAR encephalitis

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