精神病
脑炎
医学
脑脊液多细胞增多
红细胞增多
抗体
自身免疫性脑炎
自身抗体
内科学
脑脊液
免疫学
精神科
病毒
作者
Mar Guasp,Eloi Giné-Servén,Estibaliz Maudes,Mireia Rosa-Justícia,Eugenia Martínez‐Hernández,Ester Boix-Quintana,Miquel Bioque,V. Casado,Yasmina Módena-Ouarzi,Nicolau Guanyabens,Desirée Muriana,Gisela Sugranyes,Isabella Pacchiarotti,Eva Daví-Loscos,Cristina Torres-Rivas,José Ríos,Lídia Sabater,Albert Saiz,Francesc Graus,Josefina Castro-Fornieles
出处
期刊:Neurology
[Lippincott Williams & Wilkins]
日期:2021-05-12
卷期号:97 (1)
被引量:78
标识
DOI:10.1212/wnl.0000000000012191
摘要
To report the neuropsychiatric features and frequency of NMDA receptor (NMDAR) and other neuronal immunoglobulin G antibodies in patients with first episode psychosis (FEP) and to assess the performance of reported warning signs and criteria for autoimmune psychosis (AP).This was a prospective observational study of patients with FEP assessed for neuropsychiatric symptoms, serum and CSF neuronal antibodies (brain immunohistochemistry, cell-based assays, live neurons), and warning signs and criteria of AP. Previous autoimmune FEP series were reviewed.One hundred five patients were included; their median age was 30 (range 14-75) years, and 44 (42%) were female. None had neuronal antibodies. Two of 105 (2%) had CSF pleocytosis, 4 of 100 (4%) had brain MRI abnormalities, and 3 of 73 (4%) EEG alterations. Thirty-four (32%) and 39 (37%) patients fulfilled 2 sets of warning signs of AP, and 21 (20%) fulfilled criteria of possible or probable AP, yet none developed AP. The cause of FEP was psychiatric in 101 (96%) and nonpsychiatric in 4 (4%). During this study, 3 patients with psychosis caused by anti-NMDAR encephalitis were transferred to our center; 2 did not meet criteria for possible AP. Of 1,159 reported patients with FEP, only 7 (1%) had CSF studies; 36 (3%) had serum NMDAR antibodies (without definite diagnosis of AP), and 4 had CSF NMDAR antibodies (3 classic anti-NMDAR encephalitis and 1 with isolated psychiatric features).NMDAR antibodies were not found in patients with FEP unless they had anti-NMDAR encephalitis. Warning signs and criteria for AP have limited utility when neurologic symptoms are absent or paraclinical tests are normal. A diagnostic algorithm for autoimmune FEP is provided.
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