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.
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.
Brain Behav Immun. 2024 Aug;120:379-390. doi: 10.1016/j.bbi.2024.06.017. Epub 2024 Jun 19.
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.
首发精神病(FEP)是一种严重的精神健康疾病,通常在成年早期出现,其特征是对现实的感知脱节。目前的证据表明,炎症和免疫反应失调与 FEP 的发病机制有关,并且可能与阴性症状特别相关。运动训练是一种有效的抗炎刺激,可以减少持续的炎症,并可以改善一般人群的情绪特征。因此,运动可能是 FEP 的一种新的辅助治疗方法。本研究旨在评估运动对 FEP 炎症生物标志物、精神病阴性症状和生理健康标志物的影响。
从伯明翰早期精神病干预服务中招募了 17 名年轻男性(26.67±6.64 岁),并将他们随机分为运动计划组和常规治疗组(TAU)。运动计划组每周进行两到三次,运动强度目标为 60-70%最大心率(HRMax);TAU 组则接受常规治疗。在 6 周的常规运动后,评估免疫 T 辅助(Th)细胞表型和细胞因子、症状严重程度、功能健康状况和认知功能。
运动组(n=10)的参与率为 81.11%,平均运动强度为 67.54%±7.75%HRMax。这导致免疫细胞表型的有利变化,与 TAU 组相比,Th1:Th2 比值显著降低(-3.86%)(p=0.014)。运动干预后,与 TAU 组相比,血浆 IL-6 浓度也显著降低(-22.17%)(p=0.006)。运动后,IL-8 和 IL-10 两组间无统计学差异。症状上,与 TAU 组相比,运动后阴性症状显著减轻(-13.54%,阳性和阴性症状量表(PANSS)阴性)(p=0.008)。阳性或一般症状、功能结局或认知均无显著变化(均 p>0.05)。
在临床人群中,定期进行适度到剧烈的身体活动是可行的。运动是一种生理工具,能够引起 FEP 队列中显著的炎症生物标志物变化和伴随的症状改善,并且可能对目前处方的抗精神病药物未针对的症状谱有用。