Definition of a Threshold for the Plasma Aβ42/Aβ40 Ratio Measured by Single-Molecule Array to Predict the Amyloid Status of Individuals without Dementia.

Alzheimer’s disease Alzheimer’s disease screening SIMOA amyloid prediction biomarkers plasma Aβ42/Aβ40 ratio plasma amyloid

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
18 Jan 2024
Historique:
received: 15 12 2023
revised: 15 01 2024
accepted: 16 01 2024
medline: 23 1 2024
pubmed: 23 1 2024
entrez: 23 1 2024
Statut: epublish

Résumé

Alzheimer's disease (AD) is characterized by amyloid beta (Aβ) plaques and hyperphosphorylated tau in the brain. Aβ plaques precede cognitive impairments and can be detected through amyloid-positron emission tomography (PET) or in cerebrospinal fluid (CSF). Assessing the plasma Aβ42/Aβ40 ratio seems promising for non-invasive and cost-effective detection of brain Aβ accumulation. This approach involves some challenges, including the accuracy of blood-based biomarker measurements and the establishment of clear, standardized thresholds to categorize the risk of developing brain amyloid pathology. Plasma Aβ42/Aβ40 ratio was measured in 277 volunteers without dementia, 70 AD patients and 18 non-AD patients using single-molecule array. Patients (

Identifiants

pubmed: 38256246
pii: ijms25021173
doi: 10.3390/ijms25021173
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fund for Scientific Research
ID : ASP40001844
Organisme : Fund for Scientific Research
ID : CCL40010417
Organisme : Walloon Excellence in Lifesciences and Biotechnology
ID : 40010035
Organisme : Fund for Scientific Research
ID : FNRS J.0106.22
Organisme : SAO-FRA
ID : SAO-FRA 2018/0025
Organisme : UCLouvain Action de Re-533 cherche Concertée
ID : ARC21/26-114

Auteurs

Lise Colmant (L)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
Institute of Information and Communication Technologies, Electronics and Applied Mathematics, UCLouvain, 1348 Louvain-la-Neuve, Belgium.

Emilien Boyer (E)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.

Thomas Gerard (T)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.

Kristel Sleegers (K)

Complex Genetics of Alzheimer's Disease Group, VIB-UAntwerp Center for Molecular Neurology, University of Antwerp, 2000 Antwerpen, Belgium.

Renaud Lhommel (R)

Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.

Adrian Ivanoiu (A)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.

Philippe Lefèvre (P)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Institute of Information and Communication Technologies, Electronics and Applied Mathematics, UCLouvain, 1348 Louvain-la-Neuve, Belgium.

Pascal Kienlen-Campard (P)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.

Bernard Hanseeuw (B)

Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
WELBIO Department, WEL Research Institute, Avenue Pasteur, 6, 1300 Wavre, Belgium.

Classifications MeSH