A3BAD study - Analysis of amyloid aggregates in blood with atomic force microscopy as a biomarker of Alzheimer Dementia

Automatically Closed · 2020 until 2022

Fundamental Research
Monocentric project at KSSG
Automatically Closed
Start Date
End Date
Self Financed
Brief description/objective

Background: The key neuropathological feature of Alzheimer disease (AD) is the accumulation of extracellular β-amyloid (Aβ) plaques in the brain which begins long before clinical signs of dementia. Immunotherapies targeting Aβ may prevent Aβ accumulation and slow disease progression. Currently, the Aβ status of patients can only be determined by costly β-amyloid-PET-CT or invasively by lumbar puncture. Hence, novel diagnostic methods allowing screening of β-amyloid pathology are needed to select patients for future early immunotherapy preventing AD progression. Atomic force microscopy (AFM) is a technique, developed at Empa, which can resolve Aβ aggregates on red blood cell (RBC) -surfaces with high resolution. However, AFM analytics have not yet been evaluated in detecting Aβ in patient blood samples.

Objective: The primary objective of this study is to evaluate the clinical utility of AFM based analytics of Aβ-aggregates on RBC to differentiate between Aβ-positive and -negative patients presenting with cognitive decline.

Methods: Blood samples taken from patients undergoing routine work-up at the Memory Clinic, Dept. of Neurology, KSSG are analysed by AFM at Empa to detect Aβ-load. The data are correlated to clinical diagnosis.

Relevance: This study will proof the principle if an early marker of AD can be detected in blood, which would pave the road to a simple and reliable screening blood test for AD in the future.