Exercise4Psychosis: A randomised control trial assessing the effect of moderate-to-vigorous exercise on inflammatory biomarkers and negative symptom profiles in men with first-episode psychosis.

Exercise Exercise intervention First-episode psychosis Inflammation Negative symptoms Physical activity

Journal

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

Informations de publication

Date de publication:
19 Jun 2024
Historique:
received: 08 03 2024
revised: 10 06 2024
accepted: 16 06 2024
medline: 22 6 2024
pubmed: 22 6 2024
entrez: 21 6 2024
Statut: aheadofprint

Résumé

First-Episode Psychosis (FEP) is a devastating mental health condition that commonly emerges during early adulthood, and is characterised by a disconnect in perceptions of reality. Current evidence suggests that inflammation and perturbed immune responses are involved in the pathology of FEP and may be associated specifically with negative symptoms. Exercise training is a potent anti-inflammatory stimulus that can reduce persistent inflammation, and can improve mood profiles in general populations. Therefore, exercise may represent a novel adjunct therapy for FEP. The aim of this study was to assess the effect of exercise on biomarkers of inflammation, negative symptoms of psychosis, and physiological health markers in FEP. Seventeen young males (26.67 ± 6.64 years) were recruited from Birmingham Early Intervention in Psychosis Services and randomised to a 6-week exercise programme consisting of two-to-three sessions per week that targeted 60-70 % heart-rate max (HRMax), or a treatment as usual (TAU) condition. Immune T-helper (Th-) cell phenotypes and cytokines, symptom severity, functional wellbeing, and cognition were assessed before and after 6-weeks of regular exercise. Participants in the exercise group (n = 10) achieved 81.11 % attendance to the intervention, with an average exercise intensity of 67.54 % ± 7.75 % HRMax. This led to favourable changes in immune cell phenotypes, and a significant reduction in the Th1:Th2 ratio (-3.86 %) compared to the TAU group (p = 0.014). After the exercise intervention, there was also a significant reduction in plasma IL-6 concentration (-22.17 %) when compared to the TAU group (p = 0.006). IL-8, and IL-10 did not show statistically significant differences between the groups after exercise. Symptomatically, there was a significant reduction in negative symptoms after exercise (-13.54 %, Positive and Negative Syndrome Scale, (PANSS) Negative) when compared to the TAU group (p = 0.008). There were no significant change in positive or general symptoms, functional outcomes, or cognition (all p > 0.05). Regular moderate-to-vigorous physical activity is feasible and attainable in clinical populations. Exercise represents a physiological tool that is capable of causing significant inflammatory biomarker change and concomitant symptom improvements in FEP cohorts, and may be useful for treatment of symptom profiles that are not targeted by currently prescribed antipsychotic medication.

Identifiants

pubmed: 38906488
pii: S0889-1591(24)00457-4
doi: 10.1016/j.bbi.2024.06.017
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

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

Connor Dunleavy (C)

School of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, B15 2TT, United Kingdom; School of Psychology, University of Birmingham, B15 2TT, United Kingdom; Orygen, Parkville, Melbourne, Victoria 3052, Australia; Centre for Youth Mental Health, University of Melbourne, Melbourne, Victoria 3010, Australia. Electronic address: dunleavy@bham.ac.uk.

Richard J Elsworthy (RJ)

School of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, B15 2TT, United Kingdom; Centre for Human Brain Health (CHBH), University of Birmingham, Edgbaston, United Kingdom.

Stephen J Wood (SJ)

School of Psychology, University of Birmingham, B15 2TT, United Kingdom; Centre for Human Brain Health (CHBH), University of Birmingham, Edgbaston, United Kingdom; Orygen, Parkville, Melbourne, Victoria 3052, Australia; Centre for Youth Mental Health, University of Melbourne, Melbourne, Victoria 3010, Australia.

Kelly Allott (K)

Orygen, Parkville, Melbourne, Victoria 3052, Australia; Centre for Youth Mental Health, University of Melbourne, Melbourne, Victoria 3010, Australia.

Felicity Spencer (F)

School of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, B15 2TT, United Kingdom.

Rachel Upthegrove (R)

School of Psychology, University of Birmingham, B15 2TT, United Kingdom; Centre for Human Brain Health (CHBH), University of Birmingham, Edgbaston, United Kingdom; Institute for Mental Health, University of Birmingham, Birmingham, United Kingdom; Birmingham Women and Children's NHS Foundation Trust, Early Intervention in Psychosis Service, Birmingham, United Kingdom.

Sarah Aldred (S)

School of Sport, Exercise, and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, B15 2TT, United Kingdom; Centre for Human Brain Health (CHBH), University of Birmingham, Edgbaston, United Kingdom. Electronic address: s.aldred.1@bham.ac.uk.

Classifications MeSH