Eddy Roccati, Jessica Marie Collins, Michele Linda Callisaya, Jane Elizabeth Alty, Anna Elizabeth King, James John Rochfort Brady, James Clement Vickers
{"title":"来自岛屿的澳大利亚社区居民的身体活动和基于血液的神经变性生物标志物(连接衰老和神经退行性疾病的岛屿研究)。","authors":"Eddy Roccati, Jessica Marie Collins, Michele Linda Callisaya, Jane Elizabeth Alty, Anna Elizabeth King, James John Rochfort Brady, James Clement Vickers","doi":"10.1002/dad2.70166","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Physical activity, a key modifiable risk factor for dementia, has been associated with biomarkers of neurodegeneration in the central nervous system, but less is known regarding blood-based biomarkers.</p><p><strong>Methods: </strong>A total of 739 cognitively healthy participants (aged 50-83 years) from ISLAND (Island Study Linking Ageing and Neurodegenerative Disease) completed a battery of online surveys. Self-reported physical activity was assessed based on daily metabolic equivalent, and a blood sample was analyzed for serum neurofilament light chain, serum glial fibrillary acidic protein (GFAP), plasma phosphorylated tau, and genotyped for apolipoprotein E (<i>APOE</i>) ε4.</p><p><strong>Results: </strong>Higher self-reported physical activity was significantly associated with lower log-transformed concentrations of GFAP (pg/mL, <i>β</i> = -0.022, <i>P</i> = 0.009) in fully adjusted generalized linear regression models. Subgroup analysis revealed this association was only significant in <i>APOE</i> ε4 non-carriers.</p><p><strong>Discussion: </strong>This cross-sectional study provides novel evidence for the association of physical activity with blood-based biomarkers of neurodegeneration, and how <i>APOE</i> ε4 presence modifies this relationship.</p><p><strong>Highlights: </strong>We looked at a large-scale (<i>n</i> = 739) community cohort of healthy Australians > 50 years of age.Physical activity (PA) levels were related to blood-based biomarkers of neurodegeneration.Higher PA was associated with lower serum glial fibrillary acidic protein (GFAP).Apolipoprotein E ε4 and PA intensity impacted this association.This novel finding provides a foundation for targeted physical activity interventions.</p>","PeriodicalId":53226,"journal":{"name":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","volume":"17 3","pages":"e70166"},"PeriodicalIF":4.4000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12358006/pdf/","citationCount":"0","resultStr":"{\"title\":\"Physical activity and blood-based biomarkers of neurodegeneration in community dwelling Australians from ISLAND (Island Study Linking Ageing and Neurodegenerative Disease).\",\"authors\":\"Eddy Roccati, Jessica Marie Collins, Michele Linda Callisaya, Jane Elizabeth Alty, Anna Elizabeth King, James John Rochfort Brady, James Clement Vickers\",\"doi\":\"10.1002/dad2.70166\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Physical activity, a key modifiable risk factor for dementia, has been associated with biomarkers of neurodegeneration in the central nervous system, but less is known regarding blood-based biomarkers.</p><p><strong>Methods: </strong>A total of 739 cognitively healthy participants (aged 50-83 years) from ISLAND (Island Study Linking Ageing and Neurodegenerative Disease) completed a battery of online surveys. Self-reported physical activity was assessed based on daily metabolic equivalent, and a blood sample was analyzed for serum neurofilament light chain, serum glial fibrillary acidic protein (GFAP), plasma phosphorylated tau, and genotyped for apolipoprotein E (<i>APOE</i>) ε4.</p><p><strong>Results: </strong>Higher self-reported physical activity was significantly associated with lower log-transformed concentrations of GFAP (pg/mL, <i>β</i> = -0.022, <i>P</i> = 0.009) in fully adjusted generalized linear regression models. Subgroup analysis revealed this association was only significant in <i>APOE</i> ε4 non-carriers.</p><p><strong>Discussion: </strong>This cross-sectional study provides novel evidence for the association of physical activity with blood-based biomarkers of neurodegeneration, and how <i>APOE</i> ε4 presence modifies this relationship.</p><p><strong>Highlights: </strong>We looked at a large-scale (<i>n</i> = 739) community cohort of healthy Australians > 50 years of age.Physical activity (PA) levels were related to blood-based biomarkers of neurodegeneration.Higher PA was associated with lower serum glial fibrillary acidic protein (GFAP).Apolipoprotein E ε4 and PA intensity impacted this association.This novel finding provides a foundation for targeted physical activity interventions.</p>\",\"PeriodicalId\":53226,\"journal\":{\"name\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"volume\":\"17 3\",\"pages\":\"e70166\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2025-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12358006/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/dad2.70166\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/dad2.70166","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Physical activity and blood-based biomarkers of neurodegeneration in community dwelling Australians from ISLAND (Island Study Linking Ageing and Neurodegenerative Disease).
Introduction: Physical activity, a key modifiable risk factor for dementia, has been associated with biomarkers of neurodegeneration in the central nervous system, but less is known regarding blood-based biomarkers.
Methods: A total of 739 cognitively healthy participants (aged 50-83 years) from ISLAND (Island Study Linking Ageing and Neurodegenerative Disease) completed a battery of online surveys. Self-reported physical activity was assessed based on daily metabolic equivalent, and a blood sample was analyzed for serum neurofilament light chain, serum glial fibrillary acidic protein (GFAP), plasma phosphorylated tau, and genotyped for apolipoprotein E (APOE) ε4.
Results: Higher self-reported physical activity was significantly associated with lower log-transformed concentrations of GFAP (pg/mL, β = -0.022, P = 0.009) in fully adjusted generalized linear regression models. Subgroup analysis revealed this association was only significant in APOE ε4 non-carriers.
Discussion: This cross-sectional study provides novel evidence for the association of physical activity with blood-based biomarkers of neurodegeneration, and how APOE ε4 presence modifies this relationship.
Highlights: We looked at a large-scale (n = 739) community cohort of healthy Australians > 50 years of age.Physical activity (PA) levels were related to blood-based biomarkers of neurodegeneration.Higher PA was associated with lower serum glial fibrillary acidic protein (GFAP).Apolipoprotein E ε4 and PA intensity impacted this association.This novel finding provides a foundation for targeted physical activity interventions.
期刊介绍:
Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.