Abstract

Multiple lines of evidence indicate that immunological and inflammatory alterations contribute at least in a subgroup to the pathophysiology of schizophrenia. In this retrospective chart review, we investigated whether clinical factors contribute to altered cerebrospinal fluid (CSF) findings in schizophrenia-spectrum disorders. Clinical data from electronic medical records of patients with psychotic disorders (ICD-10: F20-F29) who received routine CSF diagnostics at the Department of Psychiatry and Psychotherapy, LMU Munich, Germany, were included. Chi² tests for dichotomous outcomes and independent t tests for continuous outcomes were used to compare differences between groups. A total of 331 patients were included in the analyses (43.2% female and 56.8% male). The mean age was 37.67 years (±15.58). The mean duration of illness was 71.96 months (±102.59). In all, 40% (128/320) were first-episode psychosis (FEP) patients and 60% (192/320) were multi-episode psychosis (MEP) patients. Elevated CSF protein levels were found in 19.8% and elevated CSF/serum albumin ratios (QAlb) in 29.4% of the cases. Pleocytosis was found in 6.1% of patients. MEP patients showed significantly higher mean QAlb compared with FEP patients (t(304.57) = −2.75, p = 0.006), which did not remain significant after correcting for age. QAlb elevation occurred more frequently in men (X2(1) = 14.76, p = <0.001). For treatment resistance, family history, and cMRI alterations, no significant differences in CSF-related outcomes were detected. Our work extends other retrospective cohorts confirming a relevant degree of CSF alterations in schizophrenia-spectrum disorders and shows the difficulty to relate these alterations to clinical and disease course trajectories. More research is needed to develop treatment response predictors from CSF analyses.

Details

Title
Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables
Author
Oviedo-Salcedo, Tatiana 1 ; Wagner, Elias 1   VIAFID ORCID Logo  ; Campana Mattia 1 ; Gagsteiger Anna 1 ; Strube, Wolfgang 2 ; Eichhorn, Peter 3 ; Marie-Luise, Louiset 3 ; Luykx Jurjen 4 ; de Witte Lot D 5   VIAFID ORCID Logo  ; Kahn, René S 5 ; Benros, Michael E 6   VIAFID ORCID Logo  ; Falkai, Peter 1 ; Alkomiet, Hasan 2 

 University Hospital, LMU Munich, Department of Psychiatry and Psychotherapy, Munich, Germany (GRID:grid.5252.0) (ISNI:0000 0004 1936 973X) 
 Medical Faculty, University of Augsburg, Bezirkskrankenhaus Augsburg, Department of Psychiatry, Psychotherapy and Psychosomatics, Augsburg, Germany (GRID:grid.7307.3) (ISNI:0000 0001 2108 9006) 
 Klinikum der Universität München, Ludwig Maximilians-University Munich, Institute of Laboratory Medicine, Munich, Germany (GRID:grid.411095.8) (ISNI:0000 0004 0477 2585) 
 University, Medical Center Utrecht, Brain Center Rudolf Magnus, Department of Translational Neuroscience, Utrecht, The Netherlands (GRID:grid.7692.a) (ISNI:0000000090126352) 
 Icahn School of Medicine at Mount Sinai, New York, USA (GRID:grid.59734.3c) (ISNI:0000 0001 0670 2351) 
 Copenhagen Research Centre for Mental Health, Mental Health Centre Copenhagen, Copenhagen University Hospital, Biological and Precision Psychiatry, Copenhagen, Denmark (GRID:grid.4973.9) (ISNI:0000 0004 0646 7373); University of Copenhagen, Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, Copenhagen, Denmark (GRID:grid.5254.6) (ISNI:0000 0001 0674 042X) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
21583188
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2607919707
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.