Associations of cerebral amyloid beta and tau with cognition from midlife

Author:

Gonzales Mitzi M.123,O'Donnell Adrienne45,Ghosh Saptaparni46,Thibault Emma7,Tanner Jeremy23,Satizabal Claudia L.2468,Decarli Charles S.910,Fakhri Georges El711,Johnson Keith A.71213,Beiser Alexa S.456,Seshadri Sudha2346,Pase Matthew414

Affiliation:

1. Department of Neurology Cedars Sinai Medical Center Los Angeles California USA

2. Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases University of Texas Health Science Center at San Antonio San Antonio Texas USA

3. Department of Neurology University of Texas Health Science Center at San Antonio San Antonio Texas USA

4. The Framingham Heart Study Framingham Massachusetts USA

5. Department of Biostatistics Boston University School of Public Health Boston Massachusetts USA

6. Department of Neurology Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA

7. Department of Radiology Massachusetts General Hospital and Harvard Medical School Boston Massachusetts USA

8. Department of Neurology University of California Davis Sacramento California USA

9. Department of Population Health Sciences University of Texas Health Science Center at San Antonio San Antonio Texas USA

10. Center for Neuroscience University of California Davis Davis California USA

11. Department of Radiology Yale School of Medicine New Haven United States

12. Department of Neurology Massachusetts General Hospital and Harvard Medical School Boston Massachusetts USA

13. Department of Neurology Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

14. School of Psychological Sciences Turner Institute for Brain and Mental Health Monash University Clayton VIC Australia

Abstract

AbstractINTRODUCTIONUnderstanding early neuropathological changes and their associations with cognition may aid dementia prevention. This study investigated associations of cerebral amyloid and tau positron emission tomography (PET) retention with cognition in a predominately middle‐aged community‐based cohort and examined factors that may modify these relationships.METHODS11C‐Pittsburgh compound B amyloid and 18F‐flortaucipir tau PET imaging were performed. Associations of amyloid and tau PET with cognition were evaluated using linear regression. Interactions with age, apolipoprotein E (APOE) ε4 status, and education were examined.RESULTSAmyloid and tau PET were not associated with cognition in the overall sample (N = 423; mean: 57 ± 10 years; 50% female). However, younger age (< 55 years) and APOE ε4 were significant effect modifiers, worsening cognition in the presence of higher amyloid and tau.DISCUSSIONHigher levels of Aβ and tau may have a pernicious effect on cognition among APOE ε4 carriers and younger adults, suggesting a potential role for targeted early interventions.Highlights Risk and resilience factors influenced cognitive vulnerability due to Aβ and tau. Higher fusiform tau associated with poorer visuospatial skills in younger adults. APOE ε4 interacted with Aβ and tau to worsen cognition across multiple domains.

Funder

National Institutes of Health

National Institute on Aging

Publisher

Wiley

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