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一项针对成人精神病性障碍使用利妥昔单抗的随机对照试验研究方案(RCT-Rits)。

Study protocol for a randomized controlled trial with rituximab for psychotic disorder in adults (RCT-Rits).

机构信息

Faculty of Health and Medical Sciences, University Health Care Research Centre, Örebro University, Örebro, Sweden.

Faculty of Medicine and Health, School of Medical Sciences, Örebro University, Örebro, Sweden.

出版信息

BMC Psychiatry. 2023 Oct 23;23(1):771. doi: 10.1186/s12888-023-05250-5.

Abstract

BACKGROUND

The role of inflammation in the aetiology of schizophrenia has gained wide attention and research on the association shows an exponential growth in the last 15 years. Autoimmune diseases and severe infections are risk factors for the later development of schizophrenia, elevated inflammatory markers in childhood or adolescence are associated with a greater risk of schizophrenia in adulthood, individuals with schizophrenia have increased levels of pro-inflammatory cytokines compared to healthy controls, and autoimmune diseases are overrepresented in schizophrenia. However, treatments with anti-inflammatory agents are so far of doubtful clinical relevance. The primary objective of this study is to test whether the monoclonal antibody rituximab, directed against the B-cell antigen CD20 ameliorates psychotic symptoms in adults with schizophrenia or schizoaffective disorder and to examine potential mechanisms. A secondary objective is to examine characteristics of inflammation-associated psychosis and to identify pre-treatment biochemical characteristics of rituximab responders. A third objective is to interview a subset of patients and informants on their experiences of the trial to obtain insights that rating scales may not capture.

METHODS

A proof-of-concept study employing a randomised, parallel-group, double-blind, placebo-controlled design testing the effect of B-cell depletion in patients with psychosis. 120 participants with a diagnosis of schizophrenia spectrum disorders (SSD) (ICD-10 codes F20, F25) will receive either one intravenous infusion of rituximab (1000 mg) or saline. Psychiatric measures and blood samples will be collected at baseline, week 12, and week 24 post-infusion. Brief assessments will also be made in weeks 2 and 7. Neuroimaging and lumbar puncture, both optional, will be performed at baseline and endpoints. Approximately 40 of the patients and their informants will be interviewed for qualitative analyses on the perceived changes in well-being and emotional qualities, in addition to their views on the research.

DISCUSSION

This is the first RCT investigating add-on treatment with rituximab in unselected SSD patients. If the treatment is helpful, it may transform the treatment of patients with psychotic disorders. It may also heighten the awareness of immune-psychiatric disorders and reduce stigma.

TRIAL REGISTRATION

NCT05622201, EudraCT-nr 2022-000220-37 version 2.1. registered 14 of October 2022.

摘要

背景

炎症在精神分裂症发病机制中的作用引起了广泛关注,过去 15 年来,关于该关联的研究呈指数级增长。自身免疫性疾病和严重感染是精神分裂症后期发展的风险因素,儿童或青少年时期炎症标志物升高与成年后患精神分裂症的风险增加相关,与健康对照组相比,精神分裂症患者的促炎细胞因子水平升高,自身免疫性疾病在精神分裂症中更为常见。然而,到目前为止,抗炎药物的治疗效果还存在争议。本研究的主要目的是测试针对 B 细胞抗原 CD20 的单克隆抗体利妥昔单抗是否能改善成年精神分裂症或分裂情感障碍患者的精神病症状,并研究潜在机制。次要目的是检查与炎症相关的精神病的特征,并确定利妥昔单抗治疗反应者的治疗前生化特征。第三个目标是对一部分患者和知情者进行访谈,以了解评分量表可能无法捕捉到的患者体验。

方法

采用随机、平行分组、双盲、安慰剂对照设计的概念验证研究,测试 B 细胞耗竭对精神病患者的影响。120 名符合精神分裂症谱系障碍(ICD-10 编码 F20、F25)诊断的患者将接受一次静脉输注利妥昔单抗(1000mg)或生理盐水。在输注后第 12 周和第 24 周采集精神病学测量和血液样本。在输注后第 2 周和第 7 周还将进行简短评估。神经影像学和腰椎穿刺均为可选,将在基线和终点进行。大约 40 名患者及其知情者将接受访谈,对他们的幸福感和情绪质量的变化进行定性分析,以及他们对研究的看法。

讨论

这是第一项在未选择的 SSD 患者中研究附加利妥昔单抗治疗的 RCT。如果治疗有效,它可能会改变精神病患者的治疗方式。它还可能提高对免疫精神病障碍的认识,减少污名化。

试验注册

NCT05622201,EudraCT-nr 2022-000220-37 版本 2.1,于 2022 年 10 月 14 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f704/10594806/e5b466210b96/12888_2023_5250_Fig1_HTML.jpg

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