Affiliation:
1. Department of Radiology Mayo Clinic Rochester Minnesota USA
2. Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA
3. Department of Laboratory Medicine Mayo Clinic Rochester Minnesota USA
4. Department of Nuclear Medicine Mayo Clinic Rochester Minnesota USA
5. Department of Neurology Mayo Clinic Rochester Minnesota USA
6. Department of Epidemiology and Prevention Wake Forest University School of Medicine Winston‐Salem North Carolina USA
7. Department of Psychiatry and Psychology Mayo Clinic Rochester Minnesota USA
Abstract
AbstractBACKGROUNDWe compared the ability of several plasma biomarkers versus amyloid positron emission tomography (PET) to predict rates of memory decline among cognitively unimpaired individuals.METHODSWe studied 645 Mayo Clinic Study of Aging participants. Predictor variables were age, sex, education, apolipoprotein E (APOE) ε4 genotype, amyloid PET, and plasma amyloid beta (Aβ)42/40, phosphorylated tau (p‐tau)181, neurofilament light (NfL), glial fibrillary acidic protein (GFAP), and p‐tau217. The outcome was a change in a memory composite measure.RESULTSAll plasma biomarkers, except NfL, were associated with mean memory decline in models with individual biomarkers. However, amyloid PET and plasma p‐tau217, along with age, were key variables independently associated with mean memory decline in models combining all predictors. Confidence intervals were narrow for estimates of population mean prediction, but person‐level prediction intervals were wide.DISCUSSIONPlasma p‐tau217 and amyloid PET provide useful information about predicting rates of future cognitive decline in cognitively unimpaired individuals at the population mean level, but not at the individual person level.
Funder
National Institute on Aging
Cited by
5 articles.
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