Phases of volume loss in patients with known frontotemporal lobar degeneration spectrum pathology.


Journal

Neurobiology of aging
ISSN: 1558-1497
Titre abrégé: Neurobiol Aging
Pays: United States
ID NLM: 8100437

Informations de publication

Date de publication:
05 2022
Historique:
received: 22 06 2021
revised: 14 02 2022
accepted: 16 02 2022
pubmed: 25 3 2022
medline: 26 4 2022
entrez: 24 3 2022
Statut: ppublish

Résumé

Frontotemporal lobar degeneration (FTLD) includes clinically similar FTLD-tau or FTLD-TDP proteinopathies which lack in vivo markers for accurate antemortem diagnosis. To identify early distinguishing sites of cortical atrophy between groups, we retrospectively analyzed in vivo volumetric MRI from 42 FTLD-Tau and 21 FTLD-TDP patients and validated these findings with postmortem measures of pathological burden. Our frequency-based staging model revealed distinct loci of maximal early cortical atrophy in each group, including dorsolateral and medial frontal regions in FTLD-Tau and ventral frontal and anterior temporal regions in FTLD-TDP. Sørenson-Dice calculations between proteinopathy groups showed little overlap of phases. Conversely, within-group subtypes showed good overlap between 3R- and 4R-tauopathies, and between TDP-43 Types A and C for early regions with subtle divergence between subtypes in subsequent phases of atrophy. Postmortem validation found an association of imaging phases with pathologic burden within FTLD-tau (F

Identifiants

pubmed: 35325815
pii: S0197-4580(22)00027-6
doi: 10.1016/j.neurobiolaging.2022.02.007
pmc: PMC9241163
mid: NIHMS1793212
pii:
doi:

Substances chimiques

Biomarkers 0
tau Proteins 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

95-107

Subventions

Organisme : NIA NIH HHS
ID : U01 AG052943
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG066597
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072979
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG054519
Pays : United States
Organisme : NIA NIH HHS
ID : K01 AG061277
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS109260
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

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Auteurs

Sarah E Burke (SE)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.. Electronic address: sarah.burke@pennmedicine.upenn.edu.

Jeffrey S Phillips (JS)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.

Christopher A Olm (CA)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.; Department of Radiology, Penn Image Computing & Science Lab (PICSL), Philadelphia, PA, USA.

Claire S Peterson (CS)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.; Digital Pathology Laboratory, Department of Neurology, University of Pennsylvania, Philadelphia, PA, USA.

Phillip A Cook (PA)

Department of Radiology, Penn Image Computing & Science Lab (PICSL), Philadelphia, PA, USA.

James C Gee (JC)

Department of Radiology, Penn Image Computing & Science Lab (PICSL), Philadelphia, PA, USA.

Edward B Lee (EB)

Department of Pathology and Laboratory Medicine, Center of Neurodegenerative Disease Research, Philadelphia, PA, USA.

John Q Trojanowski (JQ)

Department of Pathology and Laboratory Medicine, Center of Neurodegenerative Disease Research, Philadelphia, PA, USA.

Lauren Massimo (L)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.

David J Irwin (DJ)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.; Digital Pathology Laboratory, Department of Neurology, University of Pennsylvania, Philadelphia, PA, USA.

Murray Grossman (M)

Department of Neurology, Penn Frontotemporal Degeneration Center, Philadelphia, PA, USA.

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