Deciphering the genetic basis of chronic kidney disease towards prevention and personalized therapy
This project aims to uncover the genetic basis of chronic kidney disease (CKD) through next-generation sequencing and develop RNA-based therapies for targeted treatment and improved management.
Projectdetails
Introduction
Chronic Kidney Disease (CKD) is a public health challenge affecting millions globally. Patients have increased risks of mortality, morbidity, and progression to end-stage kidney disease (ESKD). CKD is often clinically silent, disease mechanisms are unclear, and targeted therapies are unavailable.
Background
Recent studies support considerable contributions of underappreciated monogenic aetiologies in adults with CKD, suggesting that most inherited kidney diseases remain undiagnosed, untreated, and poorly understood. Our overarching objective is to unravel the genetic basis of CKD towards early diagnosis and gene-based therapy.
Cohort Establishment
We therefore established the Israeli ESKD genetic cohort and have already recruited clinical data and samples from 2,000 participants with ESKD.
Main Objectives
Our main objectives are:
- To unravel known and novel CKD genes by interrogating high-risk groups for genetic CKD using next generation sequencing on a population level.
- To study novel monogenic CKD disease mechanisms by using patient-derived kidney organoids and mutation-specific mouse models. Specifically, we will study a newly identified WDR19 mutation leading to many adult onset-ESKD cases in the Israeli Arab-Druze population.
- To develop gene-based targeted therapies for CKD. We will focus initially on monogenic CKD secondary to gain-of-toxic-function mutations in UMOD (encoding uromodulin, a kidney-specific protein). This relatively frequent adult CKD aetiology accounts for 0.5-2% of CKD cases worldwide.
Therapeutic Approaches
Altered uromodulin's toxic effect is suitable for novel RNA-based therapies. Gene silencing of uromodulin with antisense oligonucleotides will be performed and studied, using a patient-derived in vitro model as well as a Umod mouse model.
Expected Outcomes
This project will improve CKD classification and clinical management, reveal disease mechanisms, as well as novel treatments. In a broader perspective, this project will set the stage for future clinical trials and for other RNA-based gene-specific CKD treatments.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.800.000 |
Totale projectbegroting | € 1.800.000 |
Tijdlijn
Startdatum | 1-7-2022 |
Einddatum | 30-6-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- MEDICAL RESEARCH INFRASTRUCTURE DEVELOPMENT AND HEALTH SERVICES FUND BY THE SHEBA MEDICAL CENTERpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Identification of novel diagnostic, predictive and therapeutic strategies in chronic kidney diseaseTargetCKD aims to revolutionize chronic kidney disease management by developing noninvasive diagnostics and novel therapeutics through advanced genomic technologies and interdisciplinary research. | ERC Consolid... | € 1.999.063 | 2022 | Details |
Developing RNA-editing based therapy for renal cystic ciliopathiesThis project aims to demonstrate that RNA editing can correct a pathogenic WDR19 mutation in kidney organoids, potentially leading to new therapies for genetic kidney diseases. | ERC Proof of... | € 150.000 | 2025 | Details |
Early detection, molecular mechanisms and therapeutic interventions in chronic kidney diseaseELIMINATE-CKD aims to enhance chronic kidney disease detection by developing a method to quantify nephron number using multi-omics and machine learning for improved diagnostics and therapies. | ERC Consolid... | € 2.000.000 | 2024 | Details |
Decoding diabetic kidney diseaseDECODE-DKD aims to identify novel drug targets for diabetic kidney disease through patient-centric multi-omic research and in-vitro models, advancing precision medicine and treatment options. | ERC Starting... | € 1.783.319 | 2022 | Details |
Improving Kidney Health by Targeting Urinary Biomarkers for Tubular FunctionU-Tube aims to identify urinary biomarkers for tubular function to enable early detection and treatment of progressive chronic kidney disease, improving patient outcomes. | ERC Consolid... | € 2.000.000 | 2024 | Details |
Identification of novel diagnostic, predictive and therapeutic strategies in chronic kidney disease
TargetCKD aims to revolutionize chronic kidney disease management by developing noninvasive diagnostics and novel therapeutics through advanced genomic technologies and interdisciplinary research.
Developing RNA-editing based therapy for renal cystic ciliopathies
This project aims to demonstrate that RNA editing can correct a pathogenic WDR19 mutation in kidney organoids, potentially leading to new therapies for genetic kidney diseases.
Early detection, molecular mechanisms and therapeutic interventions in chronic kidney disease
ELIMINATE-CKD aims to enhance chronic kidney disease detection by developing a method to quantify nephron number using multi-omics and machine learning for improved diagnostics and therapies.
Decoding diabetic kidney disease
DECODE-DKD aims to identify novel drug targets for diabetic kidney disease through patient-centric multi-omic research and in-vitro models, advancing precision medicine and treatment options.
Improving Kidney Health by Targeting Urinary Biomarkers for Tubular Function
U-Tube aims to identify urinary biomarkers for tubular function to enable early detection and treatment of progressive chronic kidney disease, improving patient outcomes.
Vergelijkbare projecten uit andere regelingen
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Ontwikkeling van een diagnostische test voor de vroege detectie van chronische nierschadeDit project onderzoekt de ontwikkeling van een niet-invasieve test voor de vroege detectie van chronische nierschade. | Mkb-innovati... | € 18.067 | 2024 | Details |
Kidney Disease Sweat sensor patch for Early diagnosis and Remote MonIToringThe KERMIT project aims to develop a cost-effective, disposable sweat patch for non-invasive early detection and remote monitoring of chronic kidney disease biomarkers. | EIC Pathfinder | € 3.080.623 | 2023 | Details |
Haalbaarheid Renal Tracker+Het project onderzoekt de haalbaarheid van de Renal Tracker+, een serviceproduct dat nierpatiënten helpt om de impact van levensstijlveranderingen op hun ziekte te monitoren. | Mkb-innovati... | € 20.000 | 2020 | Details |
Enabling advances in diagnosis, patient stratification and treatment for dilated cardiomyopathy patients and families.The DCM-NEXT consortium aims to enhance genetic testing and develop novel therapies for dilated cardiomyopathy by leveraging extensive clinical and omics data from 11,750 patients. | EIC Pathfinder | € 4.137.668 | 2023 | Details |
Comprehensive Analysis of RBM20-induced Dilated Cardiomyopathies using Omics Approaches and Repair InterventionsCARDIOREPAIR aims to identify and therapeutically target RBM20 mutations in dilated cardiomyopathy using high-throughput genomics and bioengineering to improve heart health outcomes. | EIC Pathfinder | € 4.349.410 | 2023 | Details |
Ontwikkeling van een diagnostische test voor de vroege detectie van chronische nierschade
Dit project onderzoekt de ontwikkeling van een niet-invasieve test voor de vroege detectie van chronische nierschade.
Kidney Disease Sweat sensor patch for Early diagnosis and Remote MonIToring
The KERMIT project aims to develop a cost-effective, disposable sweat patch for non-invasive early detection and remote monitoring of chronic kidney disease biomarkers.
Haalbaarheid Renal Tracker+
Het project onderzoekt de haalbaarheid van de Renal Tracker+, een serviceproduct dat nierpatiënten helpt om de impact van levensstijlveranderingen op hun ziekte te monitoren.
Enabling advances in diagnosis, patient stratification and treatment for dilated cardiomyopathy patients and families.
The DCM-NEXT consortium aims to enhance genetic testing and develop novel therapies for dilated cardiomyopathy by leveraging extensive clinical and omics data from 11,750 patients.
Comprehensive Analysis of RBM20-induced Dilated Cardiomyopathies using Omics Approaches and Repair Interventions
CARDIOREPAIR aims to identify and therapeutically target RBM20 mutations in dilated cardiomyopathy using high-throughput genomics and bioengineering to improve heart health outcomes.