Association of symptom severity and cerebrospinal fluid alterations in recent onset psychosis in schizophrenia-spectrum disorders - An individual patient data meta-analysis.

Blood–brain barrier CSF First episode psychosis Individual patient data Meta-analysis Schizophrenia spectrum disorders

Journal

Brain, behavior, and immunity
ISSN: 1090-2139
Titre abrégé: Brain Behav Immun
Pays: Netherlands
ID NLM: 8800478

Informations de publication

Date de publication:
10 Apr 2024
Historique:
received: 28 01 2024
revised: 03 04 2024
accepted: 09 04 2024
medline: 13 4 2024
pubmed: 13 4 2024
entrez: 12 4 2024
Statut: aheadofprint

Résumé

Neuroinflammation and blood-cerebrospinal fluid barrier (BCB) disruption could be key elements in schizophrenia-spectrum disorderś(SSDs) etiology and symptom modulation. We present the largest two-stage individual patient data (IPD) meta-analysis, investigating the association of BCB disruption and cerebrospinal fluid (CSF) alterations with symptom severity in first-episode psychosis (FEP) and recent onset psychotic disorder (ROP) individuals, with a focus on sex-related differences. Data was collected from PubMed and EMBASE databases. FEP, ROP and high-risk syndromes for psychosis IPD were included if routine basic CSF-diagnostics were reported. Risk of bias of the included studies was evaluated. Random-effects meta-analyses and mixed-effects linear regression models were employed to assess the impact of BCB alterations on symptom severity. Published (6 studies) and unpublished IPD from n = 531 individuals was included in the analyses. CSF was altered in 38.8 % of individuals. No significant differences in symptom severity were found between individuals with and without CSF alterations (SMD = -0.17, 95 %CI -0.55-0.22, p = 0.341). However, males with elevated CSF/serum albumin ratios or any CSF alteration had significantly higher positive symptom scores than those without alterations (SMD = 0.34, 95 %CI 0.05-0.64, p = 0.037 and SMD = 0.29, 95 %CI 0.17-0.41p = 0.005, respectively). Mixed-effects and simple regression models showed no association (p > 0.1) between CSF parameters and symptomatic outcomes. No interaction between sex and CSF parameters was found (p > 0.1). BCB disruption appears highly prevalent in early psychosis and could be involved in positive symptomś severity in males, indicating potential difficult-to-treat states. This work highlights the need for considering BCB breakdownand sex-related differences in SSDs clinical trials and treatment strategies.

Identifiants

pubmed: 38608742
pii: S0889-1591(24)00356-8
doi: 10.1016/j.bbi.2024.04.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Mattia Campana (M)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany. Electronic address: mattia.campana@med.uni-muenchen.de.

Vladislav Yakimov (V)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany.

Joanna Moussiopoulou (J)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany.

Isabel Maurus (I)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany.

Lisa Löhrs (L)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany.

Florian Raabe (F)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany; Max Planck Institute of Psychiatry, Munich, Germany.

Iris Jäger (I)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany.

Matin Mortazavi (M)

Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, University of Augsburg, BKH Augsburg, Augsburg, Germany.

Michael E Benros (ME)

Copenhagen Research Centre for Biological and Precision Psychiatry. Mental Health Centre Copenhagen, Copenhagen University Hospital, Copenhagen, Denmark.

Rose Jeppesen (R)

Copenhagen Research Centre for Biological and Precision Psychiatry. Mental Health Centre Copenhagen, Copenhagen University Hospital, Copenhagen, Denmark.

Gerd Meyer Zu Hörste (G)

Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.

Michael Heming (M)

Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster, Germany.

Eloi Giné-Servén (E)

Department of Psychiatry, Hospital Universitario de Navarra, Pamplona, Spain; IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.

Javier Labad (J)

Department of Mental Health, Hospital de Mataró, Consorci Sanitari del Maresme, Mataró, Spain; Translational Neuroscience Research Unit I3PT-INc-UAB, Institut de Innovació i Investigació Parc Taulí (I3PT), Institut de Neurociències, Universitat Autònoma de Barcelona, Spain.

Ester Boix (E)

Department of Mental Health, Hospital de Mataró, Consorci Sanitari del Maresme, Mataró, Spain.

Belinda Lennox (B)

Department of Psychiatry, University of Oxford and Oxford Health NHS Foundation Trust, Oxford, UK.

Ksenija Yeeles (K)

Department of Psychiatry, University of Oxford and Oxford Health NHS Foundation Trust, Oxford, UK.

Johann Steiner (J)

Department of Psychiatry, Magdeburg University Hospital, Magdeburg, Germany.

Gabriela Meyer-Lotz (G)

Department of Psychiatry, Magdeburg University Hospital, Magdeburg, Germany.

Henrik Dobrowolny (H)

Department of Psychiatry, Magdeburg University Hospital, Magdeburg, Germany.

Berend Malchow (B)

Department of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany.

Niels Hansen (N)

Department of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany.

Peter Falkai (P)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany; Max Planck Institute of Psychiatry, Munich, Germany; DZPG (German Center for Mental Health), partner site München/Augsburg, Germany.

Spyridon Siafis (S)

Department of Psychiatry and Psychotherapy, School of Medicine, Technical University Munich, Munich, Germany.

Stefan Leucht (S)

Department of Psychiatry and Psychotherapy, School of Medicine, Technical University Munich, Munich, Germany.

Sean Halstead (S)

Department of Psychiatry, School of Medicine, University of Queensland, Brisbane, Australia.

Nicola Warren (N)

Department of Psychiatry, School of Medicine, University of Queensland, Brisbane, Australia.

Dan Siskind (D)

Department of Psychiatry, School of Medicine, University of Queensland, Brisbane, Australia.

Wolfgang Strube (W)

Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, University of Augsburg, BKH Augsburg, Augsburg, Germany.

Alkomiet Hasan (A)

Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, University of Augsburg, BKH Augsburg, Augsburg, Germany; DZPG (German Center for Mental Health), partner site München/Augsburg, Germany.

Elias Wagner (E)

Department of Psychiatry and Psychotherapy, LMU University Hospital, Nussbaumstraße 7, D-80336 Munich, Germany; Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, University of Augsburg, BKH Augsburg, Augsburg, Germany; Evidence-based Psychiatry and Psychotherapy, Faculty of Medicine, University of Augsburg, Augsburg, Germany.

Classifications MeSH