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PREMEDiCARE SIGNED

PREcision MEDicine with induced pluripotent stem cells for Cardiac Arrhythmias Risk Evaluation

Total Cost €

0

EC-Contrib. €

0

Partnership

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 PREMEDiCARE project word cloud

Explore the words cloud of the PREMEDiCARE project. It provides you a very rough idea of what is the project "PREMEDiCARE" about.

vs    animal    risk    therapy    reproduce    revealed    unpredictable    combines    drugs    hpsc    qt    first    cardiac    arrhythmias    electrophysiological    screenings    proarrhythmic    sudden    male    disease    congenital    symptomatic    interdisciplinary    identical    susceptibility    genotype    manifestations    therapeutic    advancements    cells    cardiomyocytes    matched    pharmacological    patients    hipsc    female    models    predisposed    profound    diagnosis    stratification    syndromes    asymptomatic    personalised    medicine    severity    pipeline    families    poorly    molecular    cms    vulnerable    arrhythmogenic    prolongation    electrocardiogram    vitro    mutation    applicable    clinical    characterised    patient    simulate    reduce    humans    population    lqts    create    treatments    mutations    pluripotent    rare    interval    physiological    links    acquired    assays    carriers    precision    genetic    uses    drug    caused    syndrome    death    severe    long    contractile    shape    phenotype    protect    shift    safer    human    preclinical    subjects    pathogenic    safe    phenotypes    stem    arrhythmia   

Project "PREMEDiCARE" data sheet

The following table provides information about the project.

Coordinator
ISTITUTO AUXOLOGICO ITALIANO 

Organization address
address: VIA L. ARIOSTO 13
city: MILANO
postcode: 20145
website: www.auxologico.it

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Italy [IT]
 Total cost 168˙277 €
 EC max contribution 168˙277 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-10-01   to  2020-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ISTITUTO AUXOLOGICO ITALIANO IT (MILANO) coordinator 168˙277.00

Map

 Project objective

Long QT Syndrome (LQTS) is a severe arrhythmogenic condition characterised by the prolongation of the QT interval on the electrocardiogram. It is caused by genetic factors (congenital) or drugs (acquired) and sudden cardiac death can be the first manifestations of the disease. Advancements in genetic screenings have revealed profound links between genotype and phenotype for LQTS, improving diagnosis, risk stratification and therapy; However, it is still poorly understood why patients with identical pathogenic mutations have different clinical phenotypes, which factors are involved in this unpredictable disease severity and how we can protect these subjects from drug treatments that are safe in the general population. We do need improved and more physiological in vitro models to simulate arrhythmias in vitro, effective for drug testing, to identify, evaluate and study factors that shape the arrhythmogenic risk in vulnerable subjects. Here I propose a precision medicine approach that uses human pluripotent stem cells-derived cardiomyocytes (hPSC-CMs) from LQTS families (rare resources that include male, female, symptomatic and asymptomatic patients) to: i) demonstrate that the hiPSC technology can reproduce in vitro the clinical disease severity observed in symptomatic vs asymptomatic LQTS mutation carriers; ii) create an in vitro interdisciplinary pharmacological approach with proarrhythmic drugs which combines matched electrophysiological, contractile, molecular and genetic assays; iii) identify and evaluate the factors affecting the arrhythmogenic risk in predisposed subjects. This pipeline to assess arrhythmia susceptibility from patient-specific hiPSC-CMs can be applicable to other arrhythmogenic syndromes. The results of this project will contribute to reduce the use of animal models in preclinical research, to create safer, more effective drugs for humans and to promote the shift of new therapeutic approaches towards precision or personalised medicine.

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The information about "PREMEDICARE" are provided by the European Opendata Portal: CORDIS opendata.

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