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Protocol for the Psychosis Immune Mechanism Stratified Medicine (PIMS) trial: a randomised double-blind placebo-controlled trial of single-dose tocilizumab in patients with psychosis

Authors :
Foley, Éimear M
Griffiths, Sian Lowri
Murray, Alexander
Rogers, Jack
Corsi-Zuelli, Fabiana
Hickinbotham, Hannah
Warwick, Ella
Wilson, Martin
Kaser, Muzaffer
Murray, Graham K
Deakin, Bill
Jadon, Deepak
Suckling, John
Barnes, Nicholas M
Upthegrove, Rachel
Khandaker, Golam M
PIMS Collaboration
Foley, Éimear M [0000-0002-3603-3774]
Murray, Graham K [0000-0001-8296-1742]
Apollo - University of Cambridge Repository
Publication Year :
2023
Publisher :
BMJ, 2023.

Abstract

Peer reviewed: True<br />Funder: National Institute of Health Research Oxford Health Biomedical Research Centre<br />INTRODUCTION: Evidence suggests a potentially causal role of interleukin 6 (IL-6), a pleiotropic cytokine that generally promotes inflammation, in the pathogenesis of psychosis. However, no interventional studies in patients with psychosis, stratified using inflammatory markers, have been conducted to assess the therapeutic potential of targeting IL-6 in psychosis and to elucidate potential mechanism of effect. Tocilizumab is a humanised monoclonal antibody targeting the IL-6 receptor to inhibit IL-6 signalling, licensed in the UK for treatment of rheumatoid arthritis. The primary objective of this study is to test whether IL-6 contributes to the pathogenesis of first episode psychosis and to examine potential mechanisms by which IL-6 affects psychotic symptoms. A secondary objective is to examine characteristics of inflammation-associated psychosis. METHODS AND ANALYSIS: A proof-of-concept study employing a randomised, parallel-group, double-blind, placebo-controlled design testing the effect of IL-6 inhibition on anhedonia in patients with psychosis. Approximately 60 participants with a diagnosis of schizophrenia and related psychotic disorders (ICD-10 codes F20, F22, F25, F28, F29) with evidence of low-grade inflammation (IL-6≥0.7 pg/mL) will receive either one intravenous infusion of tocilizumab (4.0 mg/kg; max 800 mg) or normal saline. Psychiatric measures and blood samples will be collected at baseline, 7, 14 and 28 days post infusion. Cognitive and neuroimaging data will be collected at baseline and 14 days post infusion. In addition, approximately 30 patients with psychosis without evidence of inflammation (IL-6

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....79fb9e1ee59e115362f53d3f00a9dbbe