Recent clinical trials on Alzheimer's disease (AD) have been devised on the basis of hypotheses on the pathogenesis of the disease that nowadays are considered partly outdated and following
approximative criteria for patient selection. As a consequence, patients affected by heterogeneous
forms of AD with probable different sensitivity to active ingredients were considered. However, recent studies have suggested that several clinical phenotypes of AD exist and that the differentiation between disease subtypes can be due to the pathway followed by the AD precursor beta-amyloid (Aβ) peptide when self-assembles into amyloid aggregates in the brain. An integrated survey taking advantage of multiple marker modalities selected on the basis of the scientific evidence available today such as brain imaging and molecular biomarker analysis is perceived as a preferred solution to supply doctors in the identification of the different disease subtypes even in the early stages and therefore to develop a personalized treatment for each patient group.
In the PRAMA project we intend to build up a strategy for personalized prediction of the disease
based on the hypothesis that the main precursors of AD can form specific aggregates responsible for distinct clinical pictures of the disease with consequent differential sensitivity to drugs. In detail, a
combined biochemical, biophysical and optical spectroscopy characterization of molecular
biomarkers (mainly Ab peptide and tau protein) found in the cerebrospinal fluid (CSF) of 100
individuals including patients with progressive clinical signs of AD will be carried out. These data will
provide information on biomarker composition, structure, aggregation level and toxicity that will
constitute the proteomic profile of the biomarker content of each individual. The same patients will be
subjected to magnetic resonance imaging (MRI) followed by multiple features radiomic image
analysis. The entire set of biochemical, optical, MRI data including clinical parameters and neuropsychological evaluation of patients will be elaborated through Big Data analytics techniques to,
firstly, discover correlations among novel and gold-standard biomarkers and, then, to mine and
identify different AD phenotypes. The newest Artificial Intelligence and Machine Learning techniques
will be studied to model and process the complex high-dimensional data gathered in PRAMA. Data
analyses will also aim at discovering specific diagnostic, prognostic or predictive responses of the
different disease stages and on a personalized basis.
Overall, the PRAMA project proposal represents a perspective of high human and socio-economic
impact, with significant advantages including reducing healthcare costs and improving the well-being
of the world population in the immediate future.
Responsabile: Fabrizio Chiti
Data inizio: 22.10.20
Data conclusione: 22.04.25
CUP n. B94I20001200007
Progetto finanziato dalla Regione Toscana nell'ambito del Bando regionale Ricerca Salute 2018
COSTO COMPLESSIVO |
CONTRIBUTO REGIONE |
BENEFICIARI |
PARTNER |
COSTO COMPLESSIVO PER PARTNER |
CONTRIBUTO REGIONE PER PARTNER |
920.000,00 |
736.000,00 |
IFAC-CNR |
capofila |
320.000,00 |
256.000,00 |
Università degli Studi di Firenze |
partner |
200.000,00 |
160.000,00 |
||
AOU CAREGGI |
partner |
200.000,00 |
160.000,00 |
||
Istituto di scienze e tecnologie dell’informazione – CNR |
partner |
200.000,00 |
160.000,00 |
Ultimo aggiornamento
29.04.2025