Kim Jee Wook, Keum Musung, Byun Min Soo, Yi Dahyun, Jeon So Yeon, Jung Joon Hyung, Kong Nayeong, Chang Yoon Young, Jung Gijung, Ahn Hyejin, Lee Jun-Young, Kang Koung Mi, Sohn Chul-Ho, Lee Yun-Sang, Kim Yu Kyeong, Lee Dong Young
Department of Neuropsychiatry, Hallym University Dongtan Sacred Heart Hospital, 7 Keunjaebong-gil, Hwaseong, Gyeonggi, 18450, Republic of Korea; Department of Psychiatry, Hallym University College of Medicine, Chuncheon, Gangwon, 24252, Republic of Korea.
Department of Neuropsychiatry, Hallym University Dongtan Sacred Heart Hospital, 7 Keunjaebong-gil, Hwaseong, Gyeonggi, 18450, Republic of Korea.
J Prev Alzheimers Dis. 2025 Aug;12(7):100203. doi: 10.1016/j.tjpad.2025.100203. Epub 2025 May 16.
While many studies have shown that greater amounts or longer durations of walking are associated with a lower risk of Alzheimer's disease (AD) or cognitive decline in older adults, the neuropathological basis for this is not yet fully understood.
To examine the relationship between walking intensity and duration and longitudinal changes in Alzheimer's disease (AD)-related brain pathologies, including Aβ and tau accumulation, neurodegeneration, and white matter hyperintensity (WMH).
Data were drawn from the Korean Brain Aging Study for the Early Diagnosis and Prediction of AD, a longitudinal cohort study (initiated in 2014).
Community and memory clinic setting.
One hundred fifty-one older adults.
Participants underwent baseline and 4-year follow-up neuroimaging assessments. Lifetime walking, as measured using the Lifetime Total Physical Activity Questionnaire, was categorized by intensity (high vs. low) and duration (short ≤360 min/week vs. long >360 min/week), forming four combined walking groups. Aβ and tau deposition, neurodegeneration, and WMH volume were assessed via PET/MRI.
Long-duration or high-intensity walking was associated with significantly reduced Aβ accumulation over 4 years. The high-combined walking group showed similar benefits, while medium-combined groups did not. The effect was significant only in the early life-initiated walking subgroup. No associations were found with tau, neurodegeneration, or WMH volume.
Long-duration, high-intensity walking may reduce brain Aβ accumulation, potentially lowering AD risk, particularly when initiated before late life.
虽然许多研究表明,老年人步行量越大或时间越长,患阿尔茨海默病(AD)或认知衰退的风险越低,但其神经病理学基础尚未完全明确。
研究步行强度和时长与AD相关脑病理学纵向变化之间的关系,包括β淀粉样蛋白(Aβ)和tau蛋白积累、神经退行性变以及白质高信号(WMH)。
数据来自韩国AD早期诊断与预测脑老化研究,这是一项纵向队列研究(于2014年启动)。
社区和记忆诊所。
151名老年人。
参与者接受了基线和4年随访的神经影像学评估。使用终身总体身体活动问卷测量的终身步行量,按强度(高与低)和时长(短≤360分钟/周与长>360分钟/周)进行分类,形成四个综合步行组。通过正电子发射断层扫描/磁共振成像(PET/MRI)评估Aβ和tau蛋白沉积、神经退行性变以及WMH体积。
长时间或高强度步行与4年内Aβ积累显著减少相关。高综合步行组显示出类似益处,而中等综合组则没有。该效应仅在早年开始步行的亚组中显著。未发现与tau蛋白、神经退行性变或WMH体积有关联。
长时间、高强度步行可能会减少大脑Aβ积累,潜在降低AD风险,尤其是在晚年之前开始步行时。