Psychiatric Ratings using Intermediate Stratified Markers 2
The current nosology of neuropsychiatric disorders provides a pragmatic approach to diagnosis and treatment choice but lacks reference to quantitative biological underpinnings of disease. This weakness impedes innovative drug deve...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
CODIP
Cortical Disorganization in Psychosis. Neurophysiological...
222K€
Cerrado
PGC2018-098876-B-I00
ESTUDIOS ELECTROFISIOLOGICOS DEL LENGUAJE Y DE LA COGNICION...
61K€
Cerrado
TRIP
Translational Research into Psychiatric disorders genetics...
714K€
Cerrado
GACPD
Next Generation Sequencing to Identify Genes Underlying Extr...
100K€
Cerrado
PRISM
Psychiatric Ratings using Intermediate Stratified Markers...
16M€
Cerrado
CNS2023-144038
Herramientas diagnósticas, pronósticas y terapéuticas
384K€
Cerrado
Información proyecto PRISM 2
Duración del proyecto: 42 meses
Fecha Inicio: 2021-05-19
Fecha Fin: 2024-11-30
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
The current nosology of neuropsychiatric disorders provides a pragmatic approach to diagnosis and treatment choice but lacks reference to quantitative biological underpinnings of disease. This weakness impedes innovative drug development. To test whether a quantitative biological approach to the understanding and classification of neuropsychiatric disorders is both feasible and useful the PRISM 1 consortium was formed by academics, SMEs, patient organizations, regulators, ECNP, and EFPIA partners. PRISM 1 has now successfully identified quantitative biological parameters related to diagnosis (Schizophrenia (SZ) and Alzheimer Disease (AD)) as well as to social functioning irrespective of diagnosis. From the relationships between social function, neuroimaging, and cognitive endpoints a new neurobiological framework has emerged now needing further validation. Genetic studies of social functioning outcomes revealed known and novel loci for this phenotype. In addition, a preclinical test battery was developed, based on homologs of the clinical paradigms, to allow effective back-translation and a deepening of our neurobiological knowledge. Finally, a novel digital tool for assessing social function provided a novel, objective characterization that transcended the initial diagnostic classification and the digital readouts were associated with other study parameters. To build on outcomes of PRISM 1, PRISM 2 has three objectives. First, to determine the reproducibility of the transdiagnostic and pathophysiological relationship between DMN integrity and social dysfunction in SZ and AD that emerged from PRISM 1 and determine its potential to generalise to Major Depressive Disorders. Second, to test the causality between the quantitative variation in DMN integrity and social dysfunction. Third, to translate and communicate project results to the benefit of stakeholders, such as regulators, patients and their families, and health care providers.