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Biomarker clustering in autosomal dominant Alzheimer's disease
- Source :
- Alzheimer's and dementia 19(1), 274-284 (2023). doi:10.1002/alz.12661
- Publication Year :
- 2023
- Publisher :
- Wiley, 2023.
-
Abstract
- INTRODUCTIONAs the number of biomarkers used to study Alzheimer's disease (AD) continues to increase, it is important to understand the utility of any given biomarker, as well as what additional information a biomarker provides when compared to others.METHODSWe used hierarchical clustering to group 19 cross-sectional biomarkers in autosomal dominant AD. Feature selection identified biomarkers that were the strongest predictors of mutation status and estimated years from symptom onset (EYO). Biomarkers identified included clinical assessments, neuroimaging, cerebrospinal fluid amyloid, and tau, and emerging biomarkers of neuronal integrity and inflammation.RESULTSThree primary clusters were identified: neurodegeneration, amyloid/tau, and emerging biomarkers. Feature selection identified amyloid and tau measures as the primary predictors of mutation status and EYO. Emerging biomarkers of neuronal integrity and inflammation were relatively weak predictors.DISCUSSIONThese results provide novel insight into our understanding of the relationships among biomarkers and the staging of biomarkers based on disease progression.
- Subjects :
- Inflammation
Amyloid beta-Peptides
Epidemiology
Health Policy
diagnosis [Alzheimer Disease]
biomarkers
Amyloidogenic Proteins
tau Proteins
cerebrospinal fluid [Amyloid beta-Peptides]
Psychiatry and Mental health
Cellular and Molecular Neuroscience
genetics [tau Proteins]
Cross-Sectional Studies
machine learning
Developmental Neuroscience
cerebrospinal fluid [Biomarkers]
cerebrospinal fluid [tau Proteins]
Humans
Neurology (clinical)
ddc:610
Geriatrics and Gerontology
Autosomal dominant Alzheimer's disease
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Alzheimer's and dementia 19(1), 274-284 (2023). doi:10.1002/alz.12661
- Accession number :
- edsair.doi.dedup.....ade461e26f459486a15028d9902bed28