Abstract
Background: Subjective cognitive decline (SCD) is a self-perceived cognitive worsening without objective cognitive impairment. Due to its heterogeneity and potential risk of Alzheimer's disease (AD), baseline biomarkers to predict progression are clinically important. In the present study, cognitive trajectories during a 24-month period were compared between amyloid-positive SCD (A+SCD) and amyloid-negative SCD (A-SCD) subjects, and biomarkers associated with memory decline were investigated. Methods: Data from a prospective cohort study in Korea between 2016 and 2019 were analyzed. SCD subjects ≥50 years of age were eligible. All participants underwent neuropsychological tests, brain magnetic resonance imaging, and florbetaben positron emission tomography scans. Amyloid burden and regional volumes were measured. Cognitive changes corrected for age were compared between A+SCD and A-SCD groups. Biomarkers associated with memory decline were assessed. Results: Forty-seven SCD subjects (69.9 ± 6.7 years, mini-mental state examination (MMSE) score 27.5) were enrolled, and 31 completed at least 1 annual follow-up (mean follow-up: 24.7 months). Baseline characteristics except age, hippocampal atrophy, and white matter hyperintensities were similar between A+SCDs (n = 12, 25.6%) and A-SCDs (n = 35). A+SCD subjects showed greater decline in the verbal memory function compared with the A-SCD subjects after adjustment for age. MMSE scores decreased more in the A+SCD (1.1 in the A+SCD; 0.55 in the A-SCD), although it was not statistically significant. Amyloid burden and baseline memory score were associated with memory decline. Conclusions: Within SCD, A+SCD subjects showed faster memory decline compared with the A-SCD subjects and amyloid burden might be associated with future memory decline in SCD.
Original language | English |
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Pages (from-to) | 437-445 |
Number of pages | 9 |
Journal | Dementia and Geriatric Cognitive Disorders |
Volume | 50 |
Issue number | 5 |
DOIs | |
State | Published - 1 Jan 2022 |
Bibliographical note
Funding Information:This study was supported by Biomedical Research Institute Grant (2018B031) of Pusan National University Hospital, the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (2020R1C1C1006121), and the Ministry of Health and Welfare, HI18C0530.
Publisher Copyright:
© 2022 S. Karger AG. All rights reserved.
Keywords
- Alzheimer s disease
- Amyloid positron emission tomography
- Amyloidosis
- Cognitive decline
- Neuroimaging biomarker
- Subjective cognitive decline