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Clinical, Neuroimmunologic, and CSF Investigations in First Episode Psychosis.

Authors :
Guasp M
Giné-Servén E
Maudes E
Rosa-Justicia M
Martínez-Hernández E
Boix-Quintana E
Bioque M
Casado V
Módena-Ouarzi Y
Guanyabens N
Muriana D
Sugranyes G
Pacchiarotti I
Davi-Loscos E
Torres-Rivas C
Ríos J
Sabater L
Saiz A
Graus F
Castro-Fornieles J
Parellada E
Dalmau J
Source :
Neurology [Neurology] 2021 Jul 06; Vol. 97 (1), pp. e61-e75. Date of Electronic Publication: 2021 May 12.
Publication Year :
2021

Abstract

Objectives: 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).<br />Methods: 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.<br />Results: 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).<br />Conclusions: 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.<br /> (© 2021 American Academy of Neurology.)

Details

Language :
English
ISSN :
1526-632X
Volume :
97
Issue :
1
Database :
MEDLINE
Journal :
Neurology
Publication Type :
Academic Journal
Accession number :
33980703
Full Text :
https://doi.org/10.1212/WNL.0000000000012191