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Sökning: WFRF:(Ittyerah Ranjit) > (2020) > Longitudinal atroph...

Longitudinal atrophy in early Braak regions in preclinical Alzheimer's disease

Xie, Long (författare)
University of Pennsylvania
Wisse, Laura E.M. (författare)
Lund University,Lunds universitet,Diagnostisk radiologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Diagnostic Radiology, (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,University of Pennsylvania
Das, Sandhitsu R. (författare)
University of Pennsylvania
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Vergnet, Nicolas (författare)
University of Pennsylvania
Dong, Mengjin (författare)
University of Pennsylvania
Ittyerah, Ranjit (författare)
University of Pennsylvania
de Flores, Robin (författare)
University of Pennsylvania
Yushkevich, Paul A. (författare)
University of Pennsylvania
Wolk, David A. (författare)
University of Pennsylvania
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 (creator_code:org_t)
2020-08-26
2020
Engelska 14 s.
Ingår i: Human Brain Mapping. - : Wiley. - 1065-9471 .- 1097-0193. ; 41:16, s. 4704-4717
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A major focus of Alzheimer's disease (AD) research has been finding sensitive outcome measures to disease progression in preclinical AD, as intervention studies begin to target this population. We hypothesize that tailored measures of longitudinal change of the medial temporal lobe (MTL) subregions (the sites of earliest cortical tangle pathology) are more sensitive to disease progression in preclinical AD compared to standard cognitive and plasma NfL measures. Longitudinal T1-weighted MRI of 337 participants were included, divided into amyloid-β negative (Aβ−) controls, cerebral spinal fluid p-tau positive (T+) and negative (T−) preclinical AD (Aβ+ controls), and early prodromal AD. Anterior/posterior hippocampus, entorhinal cortex, Brodmann areas (BA) 35 and 36, and parahippocampal cortex were segmented in baseline MRI using a novel pipeline. Unbiased change rates of subregions were estimated using MRI scans within a 2-year-follow-up period. Experimental results showed that longitudinal atrophy rates of all MTL subregions were significantly higher for T+ preclinical AD and early prodromal AD than controls, but not for T− preclinical AD. Posterior hippocampus and BA35 demonstrated the largest group differences among hippocampus and MTL cortex respectively. None of the cross-sectional MTL measures, longitudinal cognitive measures (PACC, ADAS-Cog) and cross-sectional or longitudinal plasma NfL reached significance in preclinical AD. In conclusion, longitudinal atrophy measurements reflect active neurodegeneration and thus are more directly linked to active disease progression than cross-sectional measurements. Moreover, accelerated atrophy in preclinical AD seems to occur only in the presence of concomitant tau pathology. The proposed longitudinal measurements may serve as efficient outcome measures in clinical trials.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

ASHS
Brodmann area 35
cross-sectional
entorhinal cortex
hippocampus
longitudinal atrophy
MRI
preclinical Alzheimer's disease
tau

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

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