Plasma glial fibrillary acidic protein in the visual and language variants of Alzheimer's disease.

GFAP amyloid‐beta atypical Alzheimer's disease tau

Journal

Alzheimer's & dementia : the journal of the Alzheimer's Association
ISSN: 1552-5279
Titre abrégé: Alzheimers Dement
Pays: United States
ID NLM: 101231978

Informations de publication

Date de publication:
25 Mar 2024
Historique:
revised: 02 01 2024
received: 25 09 2023
accepted: 03 01 2024
medline: 26 3 2024
pubmed: 26 3 2024
entrez: 26 3 2024
Statut: aheadofprint

Résumé

Glial fibrillary acidic protein (GFAP) in plasma is a proxy for astrocytic activity and is elevated in amyloid-β (Aβ)-positive individuals, making GFAP a potential blood-based biomarker for Alzheimer's disease (AD). We assessed plasma GFAP in 72 Aβ-positive participants diagnosed with the visual or language variant of AD who underwent Aβ- and tau-PET. Fifty-nine participants had follow-up imaging. Linear regression was applied on GFAP and imaging quantities. GFAP did not correlate with Aβ- or tau-PET cross-sectionally. There was a limited positive correlation between GFAP and rates of tau accumulation, particularly in the language variant of AD, although associations were weaker after removing one outlier patient with the highest GFAP level. Among Aβ-positive AD participants with atypical presentations, plasma GFAP did not correlate with levels of AD pathology on PET, suggesting that the associations between GFAP and AD pathology might plateau during the advanced phase of the disease.

Identifiants

pubmed: 38528318
doi: 10.1002/alz.13713
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : R01-AG50603
Pays : United States

Informations de copyright

© 2024 The Authors. Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.

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Auteurs

Irene Sintini (I)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Neha Atulkumar Singh (NA)

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Danni Li (D)

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.

Michelle M Mielke (MM)

Department of Epidemiology and Prevention, Wake Forest University, Winston-Salem, North Carolina, USA.

Mary M Machulda (MM)

Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota, USA.

Christopher G Schwarz (CG)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Matthew L Senjem (ML)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Clifford R Jack (CR)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Val J Lowe (VJ)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Jonathan Graff-Radford (J)

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Keith A Josephs (KA)

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Jennifer L Whitwell (JL)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Classifications MeSH