Up to 1 000 000
of persons with diabetes suffering from NASH in France
Over 200 000
persons with cirrhosis in France having diabetes as the main cause most of whom neglected until they develop advanced disease
of patients with primary liver cancer have diabetes. Diabetes doubles to triples the risk of liver cancer
ABOUT THE PROJECT
The QUID-NASH research program has been set up by a consortium combining teams from the following partners Inserm, Assistance Publique-Hôpitaux de Paris (AP-HP), Université de Paris (Descartes and Diderot), Commissariat à l’EnergieAtomique (CEA), LaboratoiresServier and BioPredictive, Inserm being the coordinating partner.
The research program is co-funded by the partners (up to 16 million euros) andby the French State (9 million euros) through the 3rd call entitled “Recherche Hospitalo-Universitaire (RHU)”.
Non-alcoholic steatohepatitis (NASH)is a chronic liver disease particularly frequent and severe in patients with type 2 diabetes (T2D) in whom it cannot be recognized only by means of needle liver biopsy, a heavy and costly procedure poorly tolerated and accepted.
The main aim of the QUID-NASH program is to develop a virtual liver biopsy able to replace the current liver needle biopsy for the diagnosis and staging of NASH in patients with T2D. This first aim also includes a validation of diagnostic blood tests recently patented by BioPredictive.
Secondary aims of the program consist in increasing our knowledge about NASH pathophysiology with the identification of new metabolic pathwaysand drug targets, as well as relevant animal models (mouse and mini pig).
The main objective of QUID-NASH is to develop a BHV of NASH advanced and its elemental lesions by prospective study cross section of 350 patients with T2D patients
The subsequent objective of QUID-NASH is to improve and deepen our knowledge of the pathophysiology of NASH through:
I - The development and characterization of animal models of NASH...
Eventually, the project will deliver
I - Validated algorithms ready to enter the cycle of evaluation for the purpose of an introduction on the market as diagnostic biomarkers.