Your browser doesn't support javascript.
loading
Definition of a Threshold for the Plasma Aß42/Aß40 Ratio Measured by Single-Molecule Array to Predict the Amyloid Status of Individuals without Dementia.
Colmant, Lise; Boyer, Emilien; Gerard, Thomas; Sleegers, Kristel; Lhommel, Renaud; Ivanoiu, Adrian; Lefèvre, Philippe; Kienlen-Campard, Pascal; Hanseeuw, Bernard.
Afiliación
  • Colmant L; Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
  • Boyer E; Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
  • Gerard T; Institute of Information and Communication Technologies, Electronics and Applied Mathematics, UCLouvain, 1348 Louvain-la-Neuve, Belgium.
  • Sleegers K; Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
  • Lhommel R; Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
  • Ivanoiu A; Institute of Neuroscience, UCLouvain, 1200 Brussels, Belgium.
  • Lefèvre P; Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
  • Kienlen-Campard P; Complex Genetics of Alzheimer's Disease Group, VIB-UAntwerp Center for Molecular Neurology, University of Antwerp, 2000 Antwerpen, Belgium.
  • Hanseeuw B; Neurology Department, Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium.
Int J Mol Sci ; 25(2)2024 Jan 18.
Article en En | MEDLINE | ID: mdl-38256246
ABSTRACT
Alzheimer's disease (AD) is characterized by amyloid beta (Aß) plaques and hyperphosphorylated tau in the brain. Aß plaques precede cognitive impairments and can be detected through amyloid-positron emission tomography (PET) or in cerebrospinal fluid (CSF). Assessing the plasma Aß42/Aß40 ratio seems promising for non-invasive and cost-effective detection of brain Aß 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 Aß42/Aß40 ratio was measured in 277 volunteers without dementia, 70 AD patients and 18 non-AD patients using single-molecule array. Patients (n = 88) and some volunteers (n = 66) were subject to evaluation of amyloid status by CSF Aß quantification or PET analysis. Thresholds of plasma Aß42/Aß40 ratio were determined based on a Gaussian mixture model, a decision tree, and the Youden's index. The 0.0472 threshold, the one with the highest sensitivity, was retained for general population without dementia screening, and the 0.0450 threshold was retained for research and clinical trials recruitment, aiming to minimize the need for CSF or PET analyses to identify amyloid-positive individuals. These findings offer a promising step towards a cost-effective method for identifying individuals at risk of developing AD.
Asunto(s)
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Mol Sci / Int. j. mol. sci. (Online) / International journal of molecular sciences (Online) Año: 2024 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Péptidos beta-Amiloides / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Mol Sci / Int. j. mol. sci. (Online) / International journal of molecular sciences (Online) Año: 2024 Tipo del documento: Article País de afiliación: Bélgica