Rao Stephen M, Chorba Alexandria L, Helppi M J, Tuladhar Alina, Penko Amanda L, Holley Sarah, Nehls Brandon, Paulino Sabrina, Streicher Matthew C, Zhu Audrey, Bruening Kellie, Durgerian Sally, Koenig Katherine, Lowe Mark, Shin Wanyong, Jones Stephen E, Galioto Rachel, Pillai Jagan A, Bekris Lynn M, Leverenz James B, Rosenfeldt Anson B, Singh Tamanna, Beck Gerald J, Smith J Carson, Alberts Jay
Center for Brain Health, Neurological Institute, Cleveland Clinic, Cleveland, OH, United States.
Department of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, United States.
Front Aging Neurosci. 2025 May 27;17:1584115. doi: 10.3389/fnagi.2025.1584115. eCollection 2025.
The World Health Organization highlighted the potential protective role of exercise against cognitive decline, all-cause dementia, Alzheimer's disease (AD), and vascular dementia in healthy individuals. We have previously shown that exercise is particularly beneficial for older, cognitively unimpaired apolipoprotein E4 ( ε4) carriers. A key unanswered question is whether a long-term, high-intensity aerobic exercise intervention initiated in a cohort of previously inactive older individuals at genetic risk for AD has neuroprotective properties.
CYCLE-AD is a randomized, single-blind, single-center, controlled trial of a home-based, high-intensity exercise intervention involving 150 older ε4 carriers (ages 65-80 years) who are healthy, cognitively unimpaired, and physically inactive. Participants are randomized into two groups: indoor cycling (IC) or usual and customary care (UCC) (target of 75 each). IC participants exercise 3×/week on an upright stationary cycle ergometer at a moderate-vigorous intensity for 18 months. Those in the UCC group are expected to maintain enrollment levels of activity.
Comparison of IC and UCC groups on change in primary and secondary outcomes over baseline, 9-month, and 18-month evaluations. Primary outcomes are VO (Fitness), 5-trial total recall on the Rey Auditory Verbal List Learning Test (Episodic Memory), and total hippocampal volume derived from structural MRI (Brain Atrophy). Secondary outcomes include comprehensive neurocognitive and physical function test batteries, MRI scans including structural and functional connectivity measures, and blood-based biomarkers.
Over an 18-month interval, physically inactive ε4 carriers who engage in high-intensity aerobic exercise will demonstrate less cognitive decline and hippocampal atrophy than physically inactive ε4 carriers who did not participate in a formal exercise program.
Successful demonstration of a scalable, home-based, high-intensity aerobic exercise intervention in altering the trajectory of AD pathophysiology and its effects on cognitive functioning will transform AD treatment, improve patient outcomes and quality of life, and reduce healthcare costs.
世界卫生组织强调了运动对健康个体认知能力下降、全因性痴呆、阿尔茨海默病(AD)和血管性痴呆的潜在保护作用。我们之前已经表明,运动对年龄较大、认知未受损的载脂蛋白E4(ε4)携带者特别有益。一个关键的未解决问题是,在一组先前不活动且有AD遗传风险的老年人中启动的长期、高强度有氧运动干预是否具有神经保护特性。
CYCLE-AD是一项随机、单盲、单中心的对照试验,对150名年龄在65至80岁之间、健康、认知未受损且身体不活动的老年ε4携带者进行基于家庭的高强度运动干预。参与者被随机分为两组:室内骑行(IC)组或常规护理(UCC)组(每组目标人数为75人)。IC组参与者每周在直立式固定自行车测力计上以中等至剧烈强度锻炼3次,持续18个月。UCC组的参与者预计保持入组时的活动水平。
比较IC组和UCC组在基线、9个月和18个月评估时主要和次要结果的变化。主要结果包括VO(体能)、雷伊听觉词语学习测验的5次试验总回忆数(情景记忆)以及通过结构磁共振成像得出的海马总体积(脑萎缩)。次要结果包括全面的神经认知和身体功能测试组合、包括结构和功能连接测量的磁共振成像扫描以及血液生物标志物。
在18个月的时间间隔内,进行高强度有氧运动的身体不活动的ε4携带者与未参加正式运动计划的身体不活动的ε4携带者相比,认知能力下降和海马萎缩程度更低。
成功证明一种可扩展的、基于家庭的高强度有氧运动干预能够改变AD病理生理学轨迹及其对认知功能的影响,将改变AD的治疗方式,改善患者预后和生活质量,并降低医疗成本。