Coordinatore | ST GEORGE'S HOSPITAL MEDICAL SCHOOL
Organization address
address: Cranmer Terrace contact info |
Nazionalità Coordinatore | United Kingdom [UK] |
Sito del progetto | http://www.eutraf.eu |
Totale costo | 15˙681˙391 € |
EC contributo | 11˙997˙332 € |
Programma | FP7-HEALTH
Specific Programme "Cooperation": Health |
Code Call | FP7-HEALTH-2010-single-stage |
Funding Scheme | CP-IP |
Anno di inizio | 2010 |
Periodo (anno-mese-giorno) | 2010-11-01 - 2015-10-31 |
# | ||||
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1 |
ST GEORGE'S HOSPITAL MEDICAL SCHOOL
Organization address
address: Cranmer Terrace contact info |
UK (LONDON) | coordinator | 762˙762.40 |
2 |
UNIVERSITEIT MAASTRICHT
Organization address
address: Minderbroedersberg 4-6 contact info |
NL (MAASTRICHT) | participant | 1˙409˙810.60 |
3 |
CHU HOPITAUX DE BORDEAUX
Organization address
address: RUE DUBERNAT 12 contact info |
FR (TALENCE) | participant | 1˙267˙000.00 |
4 |
UNIVERSITE PIERRE ET MARIE CURIE - PARIS 6
Organization address
address: Place Jussieu 4 contact info |
FR (PARIS) | participant | 1˙031˙700.80 |
5 |
OTTO-VON-GUERICKE-UNIVERSITAET MAGDEBURG
Organization address
address: UNIVERSITAETSPLATZ 2 contact info |
DE (MAGDEBURG) | participant | 904˙113.80 |
6 |
UNIVERSITAET BERN
Organization address
address: Hochschulstrasse 4 contact info |
CH (BERN) | participant | 890˙500.00 |
7 |
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Organization address
address: University Offices, Wellington Square contact info |
UK (OXFORD) | participant | 738˙366.80 |
8 |
UNIVERSITAETSKLINIKUM ESSEN
Organization address
address: HUFELANDSTRASSE 55 contact info |
DE (ESSEN) | participant | 666˙016.00 |
9 |
ERKEM TIBBI YAYINCILIK YAZILIM GELISTIRME VE EGITIM HIZMETLERI LIMITED SIRKETI
Organization address
address: CINNAH CADDESI 98/4 contact info |
TR (ANKARA) | participant | 645˙702.40 |
10 |
THE UK HEALTH & ENVIRONMENT RESEARCH INSTITUTE
Organization address
address: PERA BUSINESS PARK, NOTTINGHAM ROAD contact info |
UK (MELTON MOWBRAY) | participant | 631˙875.00 |
11 |
Medizinische Universitaet Graz
Organization address
address: AUENBRUGGERPLATZ 2 contact info |
AT (GRAZ) | participant | 581˙516.40 |
12 |
THE UNIVERSITY OF BIRMINGHAM
Organization address
address: Edgbaston contact info |
UK (BIRMINGHAM) | participant | 555˙605.80 |
13 |
WESTFAELISCHE WILHELMS-UNIVERSITAET MUENSTER
Organization address
address: SCHLOSSPLATZ 2 contact info |
DE (MUENSTER) | participant | 368˙494.00 |
14 |
PHILIPPS UNIVERSITAET MARBURG
Organization address
address: Biegenstrasse 10 contact info |
DE (MARBURG) | participant | 312˙200.00 |
15 |
XENTION LTD
Organization address
address: "Iconix Park, London Road, Pampisford" contact info |
UK (CAMBRIDGE) | participant | 290˙345.60 |
16 |
OSYPKA AG
Organization address
address: EARL-H.-WOOD-STRASSE 1 contact info |
DE (RHEINFELDEN) | participant | 283˙150.00 |
17 |
TECHNISCHE UNIVERSITAET DRESDEN
Organization address
address: HELMHOLTZSTRASSE 10 contact info |
DE (DRESDEN) | participant | 278˙593.00 |
18 |
SANOFI-AVENTIS DEUTSCHLAND GMBH
Organization address
address: Industriepark Hoechst - Building G879 contact info |
DE (Frankfurt/Main) | participant | 237˙849.00 |
19 |
Nome Ente NON disponibile
Organization address
address: Domstrasse 11 contact info |
DE (GREIFSWALD) | participant | 100˙800.00 |
20 |
RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG
Organization address
address: SEMINARSTRASSE 2 contact info |
DE (HEIDELBERG) | participant | 40˙931.29 |
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
'The initiation and perpetuation of atrial fibrillation (AF) can be regarded as a complication of a progressive transformation of the structure and functional properties of the atria. This transformation is the result of complex and multiple changes at the molecular, cellular and organ levels which interact to form the basis for proarrhythmic mechanisms in AF. Numerous individual and environmental factors are probably involved in this profound transformation process in the atria. Therefore, we believe that progress in the diagnostics, prevention and treatment of AF requires highly integrative research from the molecule to bedside and from specific signaling pathways and electrophysiological mechanisms to population based studies. A consortium was formed providing this variety of expertises and has identified central research objectives for improvements in AF prevention and therapy. In 5 work packages focusing on basic research, new biomarkers for AF and therapeutic targets will be identified. We will study mechanisms of conduction disturbances in the atria, explore new ion channel targets for treatment of AF, identify specific alterations in the atria depending on the underlying heart disease, and evaluate beneficial effects of organ-protective compounds. Within two clinically oriented work packages the clinical application of these findings will be tested. The predictive value of diagnostic tools like serum biomarkers, 3D reconstruction of atrial conduction patterns based on high resolution body surface ECGs, and echocardiographic markers will be studied in large scale population studies. The new therapeutic targets will be explored in smaller prove-of-principle clinical trials (substrate oriented ablation, new pharmacological targets, and local gene delivery).'
With the ageing of the European population the prevalence of arrhythmia, affecting millions of people, is expected to increase. Patients with AF have higher risks of stroke, heart failure, hospitalisation and mortality. While occurrence of AF increases with age, it can affect younger people with genetic predispositions.
Due to the multiple possible causes of AF, it remains challenging to identify specific mechanisms to be targeted in therapy. The current clinical approach to AF includes antiarrhythmic drug therapy. Early AF diagnosis makes clinical interventions easier and more successful.
A project called 'The European network for translational research in atrial fibrillation' (http://www.eutraf.eu/ (EUTRAF)) was set up to study the causes, progression and treatment of AF. Better understanding of AF, new biomarkers and identifying novel therapeutics are the project's scientific goals. Through establishing a network of the centres of excellence in clinical research and private companies, scientific advancements are being translated into AF diagnostic and treatment tools.
EUTRAF is an ongoing five-year project to be completed by November 2015.
The project is steadily progressing towards ambitious technical goals to develop real-time fully automatic fibrillation electrograms analysis techniques, novel treatment options and non-invasive diagnostics tools.
Scientists are studying cellular and molecular mechanisms of AF, identifying and validating novel ion channels and transporters for future therapies. Research on animal models addresses oestrogen protection, atrial blood flow regulation and identification of the genetic components of AF to predict novel therapeutic targets.
Pre-clinical studies include measurement of fibrosis through electrograms and atrial fat infiltrations assessment through computerised tomography scans. Clinicians are using electrocardiogram-derived atrial complexity parameters to predict the outcome of therapeutic catheter ablation with increasing accuracy. Information technology infrastructure intended to support clinical decisions will help to predict and prevent the consequences AF, such as stroke and thromboembolism.
In addition to improving patient care through early diagnostics and treatment, the project is expected to decrease the cost of current AF management.