Title | Patterns of tau pathology identified with F-MK-6240 PET imaging. |
Publication Type | Journal Article |
Year of Publication | 2022 |
Authors | Kreisl WCharles, Lao PJ, Johnson A, Tomljanovic Z, Klein J, Polly K, Maas B, Laing KK, Chesebro AG, Igwe K, Razlighi QR, Honig LS, Yan X, Lee S, Mintz A, Luchsinger JA, Stern Y, Devanand DP, Brickman AM |
Journal | Alzheimers Dement |
Volume | 18 |
Issue | 2 |
Pagination | 272-282 |
Date Published | 2022 Feb |
ISSN | 1552-5279 |
Abstract | INTRODUCTION: Positron emission tomography (PET) imaging for neurofibrillary tau allows investigation of the in vivo spatiotemporal progression of Alzheimer's disease (AD) pathology. We evaluated the suitability of F-MK-6240 in a clinical sample and determined the relationships among F-MK-6240 binding, age, cognition, and cerebrospinal fluid (CSF)-based AD biomarkers. METHODS: Participants (n = 101, 72 ± 9 years, 52% women) underwent amyloid PET, tau PET, structural T1-weighted magnetic resonance imaging, and neuropsychological evaluation. Twenty-one participants had lumbar puncture for CSF measurement of amyloid beta (Aβ) , tau, and phosphorylated tau (p-tau). RESULTS: F-MK-6240 recapitulated Braak staging and correlated with CSF tau and p-tau, normalized to Aβ . F-MK-6240 negatively correlated with age across Braak regions in amyloid-positive participants, consistent with greater tau pathology in earlier onset AD. Domain-specific, regional patterns of F-MK-6240 binding were associated with reduced memory, executive, and language performance, but only in amyloid-positive participants. DISCUSSION: F-MK-6240 can approximate Braak staging across the AD continuum and provide region-dependent insights into biomarker-based AD models. |
DOI | 10.1002/alz.12384 |
Alternate Journal | Alzheimers Dement |
PubMed ID | 34057284 |
PubMed Central ID | PMC8630090 |
Grant List | R01 AG050440 / AG / NIA NIH HHS / United States P01AG07232 / / Washington Heights-Inwood Columbia Aging Project / K23AG052633 / AG / NIA NIH HHS / United States P50AG008702 / / Columbia University Alzheimer's Disease Research Center / RF1 AG054023 / AG / NIA NIH HHS / United States R01 AG038465 / AG / NIA NIH HHS / United States K99AG065506 / AG / NIA NIH HHS / United States RF1AG038465 / AG / NIA NIH HHS / United States R01AG055422 / AG / NIA NIH HHS / United States R01AG037212 / / Washington Heights-Inwood Columbia Aging Project / R01 AG072474 / AG / NIA NIH HHS / United States R01AG050440 / AG / NIA NIH HHS / United States RF1AG058067 / AG / NIA NIH HHS / United States K24AG045334 / AG / NIA NIH HHS / United States K24 AG045334 / AG / NIA NIH HHS / United States RF1AG051556-01S2 / AG / NIA NIH HHS / United States WHICAP / / Washington Heights-Inwood Columbia Aging Project / P50 AG008702 / AG / NIA NIH HHS / United States P01 AG007232 / AG / NIA NIH HHS / United States K23 AG052633 / AG / NIA NIH HHS / United States RF1 AG058067 / AG / NIA NIH HHS / United States R01 AG026158 / AG / NIA NIH HHS / United States R01AG026158 / AG / NIA NIH HHS / United States R01 AG037212 / AG / NIA NIH HHS / United States RF1AG054023 / / Washington Heights-Inwood Columbia Aging Project / UL1 TR000040 / TR / NCATS NIH HHS / United States RF1 AG051556 / AG / NIA NIH HHS / United States K99 AG065506 / AG / NIA NIH HHS / United States RF1 AG038465 / AG / NIA NIH HHS / United States UL1 TR000040 / TR / NCATS NIH HHS / United States |
Related Institute:
Brain Health Imaging Institute (BHII)