The purpose of this study is to validate a diagnostic test that combines different blood markers to identify and correctly classify patients with Alzheimer's disease (AD) compared to individuals with behavioural variant frontotemporal dementia (bvFTD, patient control) versus cognitively healthy individuals (healthy control).
The purpose of this study is to validate a new multi-parameter diagnostic test, on a well-characterised population based on new AD diagnostic criteria, that combines different types of markers, selected based on prior exploratory studies carried out by Raman Health Technologies.
Study Type
OBSERVATIONAL
Enrollment
700
AZ Sint Jan
Bruges, Belgium
UCL St Luc
Brussels, Belgium
Centre Hospitalier d'ARRAS
Arras, France
Blood markers
Multi-parameter determination: Raman laser and infrared spectroscopic markers, Metabolite-based markers (A02, A16, A22 ST01 F20 M30), Protein markers (A, A-T, B, PRO-B, C, C1, C2, PROGRANULIN), Biochemical markers (OXIDATIVE STRESS MARKERS, CTAN, ROUTINE BIOCHEMICAL MARKERS (GLUCOSE, TRIGLYCERIDES) and Genetic markers (ApoE, ApoC).
Time frame: Up to 12 months
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Hôpital neurologique Pierre Wertheimer
Bron, France
Clinique Neurologique CHRU
Lille, France
Centre Mémoire paris Nord Ile de France GH Saint-Louis Lariboisière Fernand Widal
Paris, France
Cognitive and Behavioral Disease Center and Alzheimer's Institute
Paris, France
Hospital Marqués de Valdecilla
Santander, Cantabria, Spain
Hospital Virgen de la Arrixaca
El Palmar, Murcia, Spain
CITA Alzheimer
Donostia / San Sebastian, San Sebastián, Spain
...and 6 more locations