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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.

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

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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