Abstract
ObjectivesAlzheimer’s disease (AD) is characterised by amyloid-beta accumulation (A), tau aggregation (T) and neurodegeneration (N). Vascular (V) burden has been found concomitantly with AD pathology and has synergistic effects on cognitive decline with AD biomarkers. We determined whether cognitive trajectories of AT(N) categories differed according to vascular (V) burden.MethodsWe prospectively recruited 205 participants and classified them into groups based on the AT(N) system using neuroimaging markers. Abnormal V markers were identified based on the presence of severe white matter hyperintensities.ResultsIn A+ category, compared with the frequency of Alzheimer’s pathological change category (A+T–), the frequency of AD category (A+T+) was significantly lower in V+ group (31.8%) than in V– group (64.4%) (p=0.004). Each AT(N) biomarker was predictive of cognitive decline in the V+ group as well as in the V– group (p<0.001). Additionally, the V+ group showed more severe cognitive trajectories than the V– group in the non-Alzheimer’s pathological changes (A–T+, A–N+; p=0.002) and Alzheimer’s pathological changes (p<0.001) categories.ConclusionThe distribution and longitudinal outcomes of AT(N) system differed according to vascular burdens, suggesting the importance of incorporating a V biomarker into the AT(N) system.
Funder
National Research Foundation of Korea
Future Medicine 2030 Project of the Samsung Medical Center
Institute of Information & communications Technology Planning & Evaluation
Ministry of Health Welfare, Republic of Korea
"Korea National Institute of Health" research project
Korea Health Industry Development Institute
Ministry of Health & Welfare and Ministry of science and ICT, Republic of Korea
Subject
Psychiatry and Mental health,Neurology (clinical),Surgery
Cited by
3 articles.
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