Entorhinal cortex tau, amyloid-β, cortical thickness and memory performance in non-demented subjects

Author:

Knopman David S1,Lundt Emily S2,Therneau Terry M2,Vemuri Prashanthi3,Lowe Val J3,Kantarci Kejal3,Gunter Jeffrey L3,Senjem Matthew L3,Mielke Michelle M2,Machulda Mary M4,Boeve Bradley F1,Jones David T1,Graff-Radford Jon1,Albertson Sabrina M2,Schwarz Christopher G3,Petersen Ronald C1,Jack Clifford R3

Affiliation:

1. Department of Neurology, Mayo Clinic, Rochester, MN, USA

2. Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA

3. Department of Radiology, Mayo Clinic, Rochester, MN, USA

4. Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA

Abstract

AbstractAs more biomarkers for Alzheimer’s disease and age-related brain conditions become available, more sophisticated analytic approaches are needed to take full advantage of the information they convey. Most work has been done using categorical approaches but the joint relationships of tau PET, amyloid PET and cortical thickness in their continuous distributions to cognition have been under-explored. We evaluated non-demented subjects over age 50 years in the Mayo Clinic Study of Aging, 2037 of whom had undergone 3 T MRI scan, 985 amyloid PET scan with 11C-Pittsburgh compound B (PIB) and MRI, and 577 PIB-PET, 18F-AV1451 flortaucipir PET and MRI. Participants received a nine-test cognitive battery. Three test scores (logical memory delayed recall, visual reproduction delayed recall and auditory verbal learning test delayed recall) were used to generate a memory composite z-score. We used Gradient Boosting Machine models to analyse the relationship between regional cortical thickness, flortaucipir PET signal, PIB-PET signal and memory z-scores. Age, education, sex and number of test exposures were included in the model as covariates. In this population-based study of non-demented subjects, most of the associations between biomarkers and memory z-scores accrued after 70 years of age. Entorhinal cortex exhibited the strongest associations between biomarkers and memory z-scores. Other temporal regions showed similar but attenuated associations, and non-temporal regions had negligible associations between memory z-scores and biomarkers. Entorhinal flortaucipir PET signal, PIB-PET signal and entorhinal cortical thickness were independently and additively associated with declining memory z-scores. In contrast to global PIB-PET signal where only very high amyloid-β levels were associated low memory z-scores, entorhinal flortaucipir PET signal just above background levels was associated with low memory z-scores. The lowest memory z-scores occurred with the confluence of elevated entorhinal flortaucipir PET signal and lower entorhinal cortical thickness.

Funder

NIH

Elsie and Marvin Dekelboum Family Foundation

Robert H. and Clarice Smith and Abigail Van Buren Alzheimer’s Disease Research Program

Mayo Foundation

GHR Foundation

Alexander Family Alzheimer’s Disease Research Professorship of the Mayo Clinic

Liston Award, Schuler Foundation

Mayo Foundation for Medical Education and Research

University of Southern California

NIA

Alexander Family Alzheimer’s Disease Research Professorship of the Mayo Foundation

National Institutes of Health

Department of Defense

Biogen, Roche, and Lundbeck

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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