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Physical Activity, Alzheimer Plasma Biomarkers, and Cognitionopen access

Authors
Kim, Seung AeShin, DaeunHam, HongkiKim, YeshinGu, YunaKim, Hee JinNa, Duk L.Zetterberg, HenrikBlennow, KajSeo, Sang WonJang, HyeminSeo, Sang WonNa, Duk L.Jang, HyeminKim, YoungsooHan, Sun-HoSeong, JoonKyungChoi, Jun-KyuLee, Eek-SungChin, JuheeKim, Chi-HunKim, Hee JinBok, HaesookSeo, Sang WonNa, Duk L.Jang, HyeminKim, Hee JinKang, Sung HoonKim, YeshinKim, Chi-HunKim, Si EunKim, Hang-RaiJung, Na-YeonKim, Seung JooNa, SeungheeKim, Geon HaKim, Ko WoonLee, Jin SanCho, HannaKim, Yeo JinCho, Soo HyunKim, Byeong C.Lee, Dong YoungMoon, So YoungByun, Min SooJung, GiijungYi, DahyunLee, Han NaJang, Jae-WonLee, Eek-SungJeong, Jee HyangJung, Young HeeKim, Jong HunNoh, YoungYang, HyunjungHa, YoungjiShin, Hae-EunKang, KyunghunEom, SungHuiChin, JuheeBok, HaesookKim, YoungsooHan, Sun-HoShin, Ki YoungKim, YeongshinJang, JisungYoon, ChangsikLee, Do KyungSeong, JoonKyungHam, HongkiPark, Yu HyunKim, Soo-JongByun, ByunghyunChoi, YejooLee, Na KyungWon, Hong-HeeCho, MinyoungJung, Sang-HyukLee, Dong HyunKim, BeomsuChoi, Jun-KyuSeo, JinkyuCheon, Bo KyoungKim, Youngju
Issue Date
Mar-2025
Publisher
American Medical Association
Keywords
Amyloid Beta Protein; Amyloid Beta-peptides; Biomarkers; Glial Fibrillary Acidic Protein; Neurofilament Protein L; Neurofilament Proteins; Peptide Fragments; Tau Proteins; Amyloid Beta Protein[1-40]; Amyloid Beta Protein[1-42]; Biological Marker; Glial Fibrillary Acidic Protein; Tau Protein; Amyloid Beta Protein; Neurofilament Protein; Neurofilament Protein L; Peptide Fragment; Age; Aged; Alzheimer Disease; Article; Clinical Dementia Rating Sum Of Boxes; Cognition; Cognitive Defect; Cohort Analysis; Controlled Study; Cross-sectional Study; Female; Human; International Physical Activity Questionnaire; Major Clinical Study; Male; Metabolic Equivalent; Mini Mental State Examination; Multicenter Study; Nerve Degeneration; Neurofilament; Physical Activity; South Korea; Blood; Dementia Assessment; Exercise; Middle Aged; Physiology; Very Elderly; Aged; Aged, 80 And Over; Alzheimer Disease; Amyloid Beta-peptides; Biomarkers; Cognition; Cognitive Dysfunction; Cross-sectional Studies; Exercise; Female; Glial Fibrillary Acidic Protein; Humans; Male; Mental Status And Dementia Tests; Middle Aged; Neurofilament Proteins; Peptide Fragments; Republic Of Korea; Tau Proteins
Citation
JAMA Network Open, v.8, no.3
Indexed
SCIE
SCOPUS
Journal Title
JAMA Network Open
Volume
8
Number
3
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/58332
DOI
10.1001/jamanetworkopen.2025.0096
ISSN
2574-3805
Abstract
Importance: Physical activity (PA) is a nonpharmacological intervention for dementia prevention. The association between PA and Alzheimer disease (AD) plasma biomarkers remains underexplored. Objective: To investigate the associations among PA; plasma biomarkers, including β-amyloid 42/40 (Aβ42/40), phosphorylated-tau217 (ptau217), glial fibrillary acidic protein (GFAP), and neurofilament light chain (NfL); and cognition. Design, Setting, and Participants: This cross-sectional study included participants with and without cognitive impairment recruited from multiple memory clinics in South Korea between May 2019 and May 2022. Data were analyzed from June to December 2024. Exposures: PA was assessed as metabolic equivalent task minutes per week using the International Physical Activity Questionnaire and categorized into quartiles from the lowest (Q1) to the highest (Q4). Main Outcomes and Measures: Plasma Aβ42/40, ptau217, GFAP, and NfL were measured. Cognition was assessed using the Mini-Mental State Examination (MMSE) and Clinical Dementia Rating-Sum of Boxes (CDR-SB). Results: Among 1144 participants (mean [SD] age 70.9 [8.7] years; 744 [65.0%] female), the highest PA quartile showed significantly lower ptau217 (estimate [SE], -0.14 [0.06]; P =.01) and NfL (estimate [SE], -0.12 [0.05]; P =.01) compared with the lowest quartile. Higher PA quartiles were associated with higher MMSE scores (estimate [SE]: Q2, 0.93 [0.31]; P =.003; Q3, 0.82 [0.32]; P =.009; Q4, 0.94 [0.32]; P =.004) and lower CDR-SB scores (estimate [SE]: Q2, -0.33 [0.16]; P =.04; Q3, -0.37 [0.16]; P =.02; Q4, -0.55 [0.16]; P =.001) after adjusting for age, sex, education years, and β-amyloid uptake. In subgroup analyses according to age and cognitive status, the associations of PA and plasma biomarkers with cognition were more pronounced in the older (age ≥65 years) and cognitively impaired groups compared with the younger and cognitively unimpaired groups. Conclusions and Relevance: These findings suggest that PA may help delay cognitive decline by modulating neurodegeneration and AD-specific tau pathologies. However, the cross-sectional design limits causal inference, and longitudinal studies are needed to confirm and clarify these associations. © 2025 Kim SA et al.
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