Cross-sectional associations of tau-PET signal with cognition in cognitively unimpaired adults

Val J. Lowe, Tyler J. Bruinsma, Heather J. Wiste, Hoon Ki Min, Stephen D. Weigand, Ping Fang, Matthew L. Senjem, Terry M. Therneau, Bradley F. Boeve, Keith A. Josephs, Mukesh K. Pandey, Melissa E. Murray, Kejal Kantarci, David T. Jones, Prashanthi Vemuri, Jonathan Graff-Radford, Christopher G. Schwarz, Mary M. Machulda, Michelle M. Mielke, Rosebud O. RobertsDavid S. Knopman, Ronald C. Petersen, Clifford R. Jack

Research output: Contribution to journalArticlepeer-review

16 Scopus citations


ObjectiveTo assess cross-sectional associations of neurofibrillary tangles, measured by tau-PET, with cognitive performance in cognitively unimpaired (CU) adults.MethodsTau- and amyloid-PET were performed in 579 CU participants aged 50-98 from the population-based Mayo Clinic Study of Aging. Associations between tau-PET signal in 43 brain regions and cognitive test scores were assessed using penalized linear regression. In additional models, participants were classified by normal/abnormal global amyloid-PET (A+/A-) and normal/abnormal regional tau-PET (T+/T-). Regional tau-PET cutpoints were defined as standardized uptake value ratio (SUVR) greater than the 95th percentile of tau-PET SUVR in that region among 117 CU participants aged 30-49.ResultsHigher tau-PET signal was associated with poorer memory performance in all medial temporal lobe (MTL) regions and also in the middle temporal pole and frontal olfactory regions. The largest association with tau-PET and memory z scores was seen in the entorhinal cortex; this association was independent of tau-PET signal in other brain regions. Tau-PET in the entorhinal cortex was also associated with poorer global and language performance. In the entorhinal cortex, T+ was associated with lower memory performance among both A- and A+.ConclusionsTau deposition in MTL regions, as reflected by tau-PET signal, was associated with poorer performance on memory tests in CU participants. The association with entorhinal cortex tau-PET was independent of tau-PET signal in other brain regions. Longitudinal studies are needed to understand the fate of CU participants with elevated medial temporal tau-PET signal.

Original languageEnglish (US)
Pages (from-to)E29-E39
Issue number1
StatePublished - Jul 2 2019

ASJC Scopus subject areas

  • Clinical Neurology


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