CARDIO MEF

Cardiac electro-mechanical coupling in relation to ventricular arrhythmias in the intact human heart: from cardiac mapping and speckle tracking echocardiography to biomarkers

 Coordinatore UNIVERSITY COLLEGE LONDON 

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Ms.
Nome: Malgorzata
Cognome: Kielbasa
Email: send email
Telefono: 4402030000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 221˙606 €
 EC contributo 221˙606 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-02-23   -   2017-02-22

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE LONDON

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Ms.
Nome: Malgorzata
Cognome: Kielbasa
Email: send email
Telefono: 4402030000000

UK (LONDON) coordinator 221˙606.40

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

electrical    wave    repolarization    heterogeneity    ecg    dispersion    patients    beat    strain    variability    arrhythmic    effect    data    recorded    quantify    mechanical    fingertip    photoplethysmogram    pulse    cardiac    regional    we    alternans   

 Obiettivo del progetto (Objective)

'Cardiac electro-mechanical coupling is known to contribute to sudden cardiac death, a significant public health issue, but its role in the intact human heart is undetermined, mainly because of the lack of data. The proposed work will: Record a unique data-set from patients acquired prior to cardiac surgery. The studies include high-density electrical mapping of the ventricles, speckle-tracking echocardiography, ECG and photoplethysmography. We will quantify the relationship between regional strain and the dispersion of repolarization, and develop a non-invasive biomarker of dispersion of repolarization, which incorporates strain heterogeneity and T-wave morphology. We will quantify the contribution of the regional strain on the spatiotemporal organization of repolarization alternans, and determine the effect of changes in the cardiac strain on the ECG-based indices of alternans. Additionally, we will develop an algorithm for the detection of pulse wave alternans in the photoplethysmogram recorded from the finger, and develop a mobile application to detect repolarization alternans from a fingertip pulse wave using the built-in camera lens. We hypothesize that: 1) Alterations in the strain of the myocardium have a direct, predictable effect on electrophysiology: changing action potential duration. 2) In patients with coronary artery diseases, mechanical heterogeneity contributes to electrical heterogeneity, creating a pro-arrhythmic substrate. 3) Changes in cardiac load alter the magnitude and the spatial distribution of beat-to-beat repolarization alternans. Mechanical heterogeneity enhances the degree of regional discordance of alternans and increases the arrhythmic risk. 4) The beat-to-beat variability of repolarization is coupled to the variability of contraction, and can be detected in the pulse wave recorded from a fingertip photoplethysmogram. Outputs from this project are expected to have an impact on the understanding and prediction of ventricular arrhythmia'

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