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Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables
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 schi...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654913/ https://www.ncbi.nlm.nih.gov/pubmed/34880213 http://dx.doi.org/10.1038/s41398-021-01751-7 |
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author | Oviedo-Salcedo, Tatiana Wagner, Elias Campana, Mattia Gagsteiger, Anna Strube, Wolfgang Eichhorn, Peter Louiset, Marie-Luise Luykx, Jurjen de Witte, Lot D. Kahn, René S. Benros, Michael E. Falkai, Peter Hasan, Alkomiet |
author_facet | Oviedo-Salcedo, Tatiana Wagner, Elias Campana, Mattia Gagsteiger, Anna Strube, Wolfgang Eichhorn, Peter Louiset, Marie-Luise Luykx, Jurjen de Witte, Lot D. Kahn, René S. Benros, Michael E. Falkai, Peter Hasan, Alkomiet |
author_sort | Oviedo-Salcedo, Tatiana |
collection | PubMed |
description | 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 (Q(Alb)) in 29.4% of the cases. Pleocytosis was found in 6.1% of patients. MEP patients showed significantly higher mean Q(Alb) compared with FEP patients (t((304.57)) = −2.75, p = 0.006), which did not remain significant after correcting for age. Q(Alb) elevation occurred more frequently in men (X(2)((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. |
format | Online Article Text |
id | pubmed-8654913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86549132021-12-27 Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables Oviedo-Salcedo, Tatiana Wagner, Elias Campana, Mattia Gagsteiger, Anna Strube, Wolfgang Eichhorn, Peter Louiset, Marie-Luise Luykx, Jurjen de Witte, Lot D. Kahn, René S. Benros, Michael E. Falkai, Peter Hasan, Alkomiet Transl Psychiatry Article 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 (Q(Alb)) in 29.4% of the cases. Pleocytosis was found in 6.1% of patients. MEP patients showed significantly higher mean Q(Alb) compared with FEP patients (t((304.57)) = −2.75, p = 0.006), which did not remain significant after correcting for age. Q(Alb) elevation occurred more frequently in men (X(2)((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. Nature Publishing Group UK 2021-12-08 /pmc/articles/PMC8654913/ /pubmed/34880213 http://dx.doi.org/10.1038/s41398-021-01751-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oviedo-Salcedo, Tatiana Wagner, Elias Campana, Mattia Gagsteiger, Anna Strube, Wolfgang Eichhorn, Peter Louiset, Marie-Luise Luykx, Jurjen de Witte, Lot D. Kahn, René S. Benros, Michael E. Falkai, Peter Hasan, Alkomiet Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title | Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title_full | Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title_fullStr | Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title_full_unstemmed | Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title_short | Cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
title_sort | cerebrospinal fluid abnormalities in first- and multi-episode schizophrenia-spectrum disorders: impact of clinical and demographical variables |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654913/ https://www.ncbi.nlm.nih.gov/pubmed/34880213 http://dx.doi.org/10.1038/s41398-021-01751-7 |
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