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Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers.

Qin Chen | Bradley F Boeve | Christopher G Schwarz | Robert Reid | Nirubol Tosakulwong | Timothy G Lesnick | Jessica Bove | Patrick Brannelly | Danielle Brushaber | Giovanni Coppola | Christina Dheel | Bradford C Dickerson | Susan Dickinson | Kelley Faber | Julie Fields | Jamie Fong | Tatiana Foroud | Leah Forsberg | Ralitza H Gavrilova | Debra Gearhart | Nupur Ghoshal | Jill Goldman | Jonathan Graff-Radford | Neill R Graff-Radford | Murray Grossman | Dana Haley | Hilary W Heuer | Ging-Yuek R Hsiung | Edward Huey | David J Irwin | Clifford R Jack | David T Jones | Lynne Jones | Anna M Karydas | David S Knopman | John Kornak | Joel Kramer | Walter Kremers | Walter A Kukull | Maria Lapid | Diane Lucente | Codrin Lungu | Ian R A Mackenzie | Masood Manoochehri | Scott McGinnis | Bruce L Miller | Rodney Pearlman | Leonard Petrucelli | Madeline Potter | Rosa Rademakers | Eliana M Ramos | Katherine P Rankin | Katya Rascovsky | Pheth Sengdy | Leslie Shaw | Jeremy Syrjanen | Nadine Tatton | Joanne Taylor | Arthur W Toga | John Trojanowski | Sandra Weintraub | Bonnie Wong | Adam L Boxer | Howie Rosen | Zbigniew Wszolek | Kejal Kantarci | LEFFTDS Consortium
Neurobiology of aging | 2019

Our aim was to investigate the patterns and trajectories of white matter (WM) diffusion abnormalities in microtubule-associated protein tau (MAPT) mutations carriers. We studied 22 MAPT mutation carriers (12 asymptomatic, 10 symptomatic) and 20 noncarriers from 8 families, who underwent diffusion tensor imaging (DTI) and a subset (10 asymptomatic, 6 symptomatic MAPT mutation carriers, and 10 noncarriers) were followed annually (median = 4 years). Cross-sectional and longitudinal changes in mean diffusivity (MD) and fractional anisotropy were analyzed. Asymptomatic MAPT mutation carriers had higher MD in entorhinal WM, which propagated to the limbic tracts and frontotemporal projections in the symptomatic stage compared with noncarriers. Reduced fractional anisotropy and increased MD in the entorhinal WM were associated with the proximity to estimated and actual age of symptom onset. The annualized change of entorhinal MD on serial DTI was accelerated in MAPT mutation carriers compared with noncarriers. Entorhinal WM diffusion abnormalities precede the symptom onset and track with disease progression in MAPT mutation carriers. Our cross-sectional and longitudinal data showed a potential clinical utility for DTI to track neurodegenerative disease progression for MAPT mutation carriers in clinical trials.

Pubmed ID: 31585367 RIS Download

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: P30 AG013854
  • Agency: NIA NIH HHS, United States
    Id: K24 AG045333
  • Agency: NIA NIH HHS, United States
    Id: U24 AG021886
  • Agency: NIA NIH HHS, United States
    Id: P30 AG062421
  • Agency: NIA NIH HHS, United States
    Id: R01 AG040042
  • Agency: NIA NIH HHS, United States
    Id: RF1 AG057547
  • Agency: NIA NIH HHS, United States
    Id: P01 AG019724
  • Agency: NIA NIH HHS, United States
    Id: P30 AG062677
  • Agency: NIA NIH HHS, United States
    Id: U01 AG045390
  • Agency: NINDS NIH HHS, United States
    Id: U54 NS092089
  • Agency: NINDS NIH HHS, United States
    Id: U01 NS100620
  • Agency: NIA NIH HHS, United States
    Id: P50 AG016574
  • Agency: NIA NIH HHS, United States
    Id: P01 AG017586
  • Agency: NIA NIH HHS, United States
    Id: U19 AG063911
  • Agency: NIA NIH HHS, United States
    Id: U01 AG016976

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