4.7 Article

Temporal T807 binding correlates with CSF tau and phospho-tau in normal elderly

Journal

NEUROLOGY
Volume 87, Issue 9, Pages 920-926

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000003050

Keywords

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Funding

  1. National Institute on Aging [P01 AG36694, R01 AG046396]
  2. Massachusetts Alzheimer's Disease Research Center [P50 AG005134]
  3. Harvard NeuroDiscovery Center Biomarker Study
  4. Parkinson's Disease Biomarkers Program [NINDS U01 NS082157]
  5. Harvard Clinical and Translational Science Center [8UL1 TR000170-05, 1UL1 TR001102-02]
  6. National Center for Advancing Translational Science
  7. BrightFocus Foundation
  8. American Brain Foundation/American Academy of Neurology
  9. NIA [K23 AG049087]
  10. NIH [U01 NS082157]
  11. US Department of Defense
  12. M.E.M.O. Hoffman Foundation

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Objective: To better understand cross-sectional relationships between CSF and PET measures of tau pathology, we compared regional and global measures of F-18-T807 (AV-1451) PET to CSF protein levels of total tau (t-tau), phosphorylated tau (p-tau), and beta-amyloid 1-42 (A beta 42). Methods: T-tau, p-tau, and A beta 42 levels were assessed using INNOTEST xMAP immunoassays. Linear regression was used to compare regional and global measures of F-18-T807 standardized uptake value ratios (SUVR) to CSF protein levels using data from 31 cognitively unimpaired elderly participants in the Harvard Aging Brain study. Results: After controlling for sex and age, total cortical F-18-T807 binding was significantly correlated with p-tau (partial r = 0.48; p < 0.01) and at trend level with t-tau (partial r = 0.30; p = 0.12). Regional F-18-T807 measures were more strongly correlated with CSF protein levels than the global measure, with both t-tau and p-tau significantly correlated with F-18-T807 SUVR in entorhinal, parahippocampal, and inferior temporal cortical regions (partial r = 0.53-0.73). Peak correlations between CSF and PET measures of tau were similar to those between CSF and PET measures of amyloid burden. Finally, we observed significantly higher temporal T807 SUVR in individuals with high amyloid burden. Conclusions: These data support the link between F-18-T807 PET and CSF measures of tau pathology. In these cognitively normal individuals with F-18-T807 binding largely restricted to the temporal lobe, F-18-T807 SUVR in temporal regions appeared more reflective of CSF t-tau and p-tau than a total cortical measure.

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