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Tau-neurodegeneration mismatch reveals vulnerability and resilience to comorbidities in Alzheimer's continuum

Lyu, Xueying (author)
University of Pennsylvania
Duong, Michael Tran (author)
University of Pennsylvania
Xie, Long (author)
University of Pennsylvania
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de Flores, Robin (author)
University of Caen Normandy
Richardson, Hayley (author)
University of Pennsylvania
Hwang, Gyujoon (author)
University of Pennsylvania
Wisse, Laura E.M. (author)
Lund University,Lunds universitet,Diagnostisk radiologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Diagnostic Radiology, (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Clinical Memory Research,Lund University Research Groups
DiCalogero, Michael (author)
University of Pennsylvania
McMillan, Corey T. (author)
University of Pennsylvania
Robinson, John L. (author)
University of Pennsylvania
Xie, Sharon X. (author)
University of Pennsylvania
Lee, Edward B. (author)
University of Pennsylvania
Irwin, David J. (author)
University of Pennsylvania
Dickerson, Bradford C. (author)
Massachusetts General Hospital
Davatzikos, Christos (author)
University of Pennsylvania
Nasrallah, Ilya M. (author)
University of Pennsylvania
Yushkevich, Paul A. (author)
University of Pennsylvania
Wolk, David A. (author)
University of Pennsylvania
Das, Sandhitsu R. (author)
University of Pennsylvania
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 (creator_code:org_t)
English.
In: Alzheimer's and Dementia. - 1552-5260.
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • INTRODUCTION: Variability in relationship of tau-based neurofibrillary tangles (T) and neurodegeneration (N) in Alzheimer's disease (AD) arises from non-specific nature of N, modulated by non-AD co-pathologies, age-related changes, and resilience factors. METHODS: We used regional T-N residual patterns to partition 184 patients within the Alzheimer's continuum into data-driven groups. These were compared with groups from 159 non-AD (amyloid “negative”) patients partitioned using cortical thickness, and groups in 98 patients with ante mortem MRI and post mortem tissue for measuring N and T, respectively. We applied the initial T-N residual model to classify 71 patients in an independent cohort into predefined groups. RESULTS: AD groups displayed spatial T-N mismatch patterns resembling neurodegeneration patterns in non-AD groups, similarly associated with non-AD factors and diverging cognitive outcomes. In the autopsy cohort, limbic T-N mismatch correlated with TDP-43 co-pathology. DISCUSSION: T-N mismatch may provide a personalized approach for determining non-AD factors associated with resilience/vulnerability in AD.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

aging
Alzheimer's disease
co-pathologies
multi-modality imaging
neurodegeneration
post mortem
tau

Publication and Content Type

art (subject category)
ref (subject category)

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