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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

0

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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.

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

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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