EXTOD-Immune:一项随机对照试验,旨在研究远程监控的家庭运动干预能否减少 1 型糖尿病患者的疾病活动。

IF 3.9 Q1 SPORT SCIENCES BMJ Open Sport & Exercise Medicine Pub Date : 2024-08-30 eCollection Date: 2024-01-01 DOI:10.1136/bmjsem-2024-002144
Megan Quickfall, Matthew Cocks, Heather M Long, Francesca Di Rosa, Robert Andrews, Parth Narendran, Katie Hesketh, Alex J Wadley
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引用次数: 0

摘要

1 型糖尿病(T1D)是一种慢性自身免疫性疾病,其适应性免疫系统以胰岛分泌胰岛素的 β 细胞为目标,从而导致对外源性胰岛素治疗的依赖。胰岛抗原特异性细胞毒性(CD8+)T细胞是T1D自身免疫的主要参与者。有数据表明,经常锻炼可保护新近确诊的T1D患者的β细胞功能,但胰岛反应性CD8+ T细胞的作用尚不清楚。本研究将采用随机交叉设计,确定为期 12 周的运动计划对 20 名在过去 3 年中被诊断为 T1D 的成人外周血中小岛反应型 CD8+ T 细胞的频率和增殖状态的影响。运动干预将包括每周三次高强度间歇训练(6-10 次,每次 1 分钟,间隔时间大于最大心率的 80%,休息 1 分钟),持续时间从 14 分钟逐渐增加到 22 分钟。在对照组和淘汰组期间,将保持惯常的体育锻炼和饮食习惯。在第 0、12、24 和 36 周,将采集空腹血样,以量化胰岛反应型 CD8+ T 细胞的频率、表型和增殖活性(主要结果)以及各种临床参数。在每个研究组开始和结束时,还将使用 14 天连续血糖监测对血糖控制情况进行评估。研究结果可为开展大规模试验提供依据,以评估在常规临床护理中实施运动的情况,尤其是对于新近诊断出患有 T1D 的患者,因为此时维持 β 细胞功能对于对抗疾病进展至关重要。试验注册号:ISRCTN79006041。
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EXTOD-Immune: a randomised controlled trial to investigate whether a remotely monitored, home-based exercise intervention can reduce disease activity in people with type 1 diabetes.

Type 1 diabetes (T1D) is a chronic autoimmune disease in which the adaptive immune system targets insulin-producing β-cells of pancreatic islets, leading to dependence on exogenous insulin therapy. Cytotoxic (CD8+) T-cells specific for islet antigens are major players in T1D autoimmunity. Data indicate that regular exercise may preserve β-cell function in people recently diagnosed with T1D, but the role of islet-reactive CD8+ T-cells is unclear. In a randomised crossover design, this study will determine the impact of a 12-week exercise programme on the frequency and proliferative state of islet-reactive CD8+ T-cells in the peripheral blood of 20 adults diagnosed with T1D within the past 3 years. The exercise intervention will consist of three high-intensity interval training sessions per week (6-10 1 min intervals >80% maximum heart rate, with 1 min rest), the duration of which will incrementally increase from 14 to 22 min. Habitual physical activity and diet will be maintained during control and washout periods. At weeks 0, 12, 24 and 36, a fasting blood sample will be collected to quantify the frequency, phenotype and proliferative activity of islet-reactive CD8+ T-cells (primary outcome) and various clinical parameters. Glycaemic control will also be evaluated using 14-day continuous glucose monitoring at the start and end of each study arm. Findings may provide a rationale for conducting large-scale trials to evaluate the implementation of exercise into routine clinical care, particularly for people recently diagnosed with T1D when maintenance of β-cell function is critical to counteract disease progression. Trial registration number: ISRCTN79006041.

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CiteScore
7.10
自引率
4.20%
发文量
106
审稿时长
20 weeks
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