Mapping the Connectome Dynamics of Trauma Psychopathology
Exposure to a traumatic event can induce psycho-physiological reactions and symptoms that in most people recede over time. A minority of trauma-exposed individuals develop posttraumatic stress disorder (PTSD), characterized by sev...
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Información proyecto TraumaNeuroInsight
Duración del proyecto: 59 meses
Fecha Inicio: 2024-10-01
Fecha Fin: 2029-09-30
Líder del proyecto
TEL AVIV UNIVERSITY
No se ha especificado una descripción o un objeto social para esta compañía.
TRL
4-5
Presupuesto del proyecto
2M€
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
Exposure to a traumatic event can induce psycho-physiological reactions and symptoms that in most people recede over time. A minority of trauma-exposed individuals develop posttraumatic stress disorder (PTSD), characterized by severe functional and emotional impairment. The global burden of PTSD is estimated in the hundreds of billions of Euros and millions of years lived with disability. Individual differences in neurobiological vulnerability to traumatic stress have been studied extensively, yet the impact of neuroscience on clinical application is minimal. The proposed work aims to address this gap using three work packages (WPs). WP1 will establish a detailed open-access database to study the impact of traumatic stress on brain structure/function connectome: 1000 participants with PTSD, 1000 trauma-exposed healthy, 1000 non-exposed. WP2 is a longitudinal study of the effects of trauma exposure. It will delineate long-term trajectories of stress-related symptoms and corresponding connectome dynamics. Building on already collected data from 579 veterans who were followed over four years, starting with a pre-exposure baseline, we will add two new data points, at 7- and 9-year post-exposure, to reveal long-term adaptation patterns. WP3 is a 3-armed randomized controlled trial to test the impact of MRI-guided neurostimulation of cortico-hippocampal networks on brain connectivity patterns and severity of memory symptoms. We target cortico-hippocampal connections with broad impact on cortical circuitry, consistent with our focus on whole-brain connectome correlates. Moving beyond separate analyses of brain structure and function in relation to a heterogeneous definition of PTSD, we will use combined structure/function modeling in relation to specific symptoms. Together the proposed work is expected to redetermine the transaction between neuroscience and clinical research in relation to trauma psychopathology.