FLIP

Fatty liver: Inhibition of Progression

 Coordinatore ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS 

 Organization address address: 3 Avenue Victoria
city: PARIS
postcode: 75004

contact info
Titolo: Mr.
Nome: Christophe
Cognome: Misse
Email: send email
Telefono: +33 1 44 84 17 70
Fax: +33 1 44 84 17 88

 Nazionalità Coordinatore France [FR]
 Sito del progetto http://www.flip-fp7.eu/
 Totale costo 7˙808˙902 €
 EC contributo 5˙983˙477 €
 Programma FP7-HEALTH
Specific Programme "Cooperation": Health
 Code Call FP7-HEALTH-2009-single-stage
 Funding Scheme CP-FP
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-01-01   -   2013-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS

 Organization address address: 3 Avenue Victoria
city: PARIS
postcode: 75004

contact info
Titolo: Mr.
Nome: Christophe
Cognome: Misse
Email: send email
Telefono: +33 1 44 84 17 70
Fax: +33 1 44 84 17 88

FR (PARIS) coordinator 957˙876.10
2    UNIVERSITY OF NEWCASTLE UPON TYNE

 Organization address address: Kensington Terrace 6
city: NEWCASTLE UPON TYNE
postcode: NE1 7RU

contact info
Titolo: Ms.
Nome: Aleona
Cognome: Blinova
Email: send email
Telefono: +44 191 282 4528
Fax: +44 191 282 4524

UK (NEWCASTLE UPON TYNE) participant 1˙303˙548.00
3    UNIVERSITA DEGLI STUDI DI TORINO

 Organization address address: Via Giuseppe Verdi 8
city: TORINO
postcode: 10124

contact info
Titolo: Dr.
Nome: Elisabetta
Cognome: Bugianesi
Email: send email
Telefono: +39 0116336217
Fax: +39 0116335927

IT (TORINO) participant 533˙597.00
4    Biopredictive

 Organization address address: RUE DU BAC 40
city: PARIS
postcode: 75007

contact info
Titolo: Mr.
Nome: Jean-Marie
Cognome: Castille
Email: send email
Telefono: +33 145 44 30 64

FR (PARIS) participant 361˙400.00
5    REGION HOVEDSTADEN

 Organization address address: KONGENS VAENGE 2
city: HILLEROD
postcode: 3400

contact info
Titolo: Ms.
Nome: Kate
Cognome: Livemore
Email: send email
Telefono: +45 3338 3885
Fax: +45 3332 4240

DK (HILLEROD) participant 349˙873.00
6    UNIVERSITAET BERN

 Organization address address: Hochschulstrasse 4
city: BERN
postcode: 3012

contact info
Titolo: Prof.
Nome: Jean-François
Cognome: Dufour
Email: send email
Telefono: 41316328729
Fax: 416314997

CH (BERN) participant 348˙234.00
7    MEDIZINISCHE UNIVERSITAET WIEN

 Organization address address: SPITALGASSE 23
city: WIEN
postcode: 1090

contact info
Nome: Josef
Cognome: Smolen
Email: send email
Telefono: +43 1 40400 4300
Fax: +43 1 40400 4306

AT (WIEN) participant 340˙156.80
8    ALMA MATER STUDIORUM-UNIVERSITA DI BOLOGNA

 Organization address address: Via Zamboni 33
city: BOLOGNA
postcode: 40126

contact info
Titolo: Dr.
Nome: Diego
Cognome: Torresan
Email: send email
Telefono: +39 051 2099373
Fax: +39 051 2098115

IT (BOLOGNA) participant 268˙100.00
9    UNIVERSITA DEGLI STUDI DI FIRENZE

 Organization address address: Piazza San Marco 4
city: Florence
postcode: 50121

contact info
Titolo: Prof.
Nome: Fabio
Cognome: Marra
Email: send email
Telefono: 390554000000
Fax: 39055417123

IT (Florence) participant 237˙040.00
10    Servicio Andaluz de Salud

 Organization address address: AVENIDA DE LA CONSTITUCION 18
city: SEVILLA
postcode: 41071

contact info
Titolo: Dr.
Nome: Manuel
Cognome: Romero-Gómez
Email: send email
Telefono: +34 955015761
Fax: +34 955015899

ES (SEVILLA) participant 230˙200.00
11    ALMA CONSULTING GROUP SAS

 Organization address address: Domaine des Bois d'Houlbec
city: HOULBEC COCHEREL
postcode: 27120

contact info
Titolo: Mr.
Nome: Franck
Cognome: Noumbissie
Email: send email
Telefono: +33 1 41 49 12 59

FR (HOULBEC COCHEREL) participant 229˙720.00
12    FONDAZIONE ITALIANA FEGATO ONLUS

 Organization address address: "AREA SCIENCE PARK, BLDG Q, SS14, KM 163.5"
city: TRIESTE
postcode: 34012

contact info
Titolo: Ms.
Nome: Sabrina
Cognome: Corsucci
Email: send email
Telefono: +39 040375 7838
Fax: +39 040375 7832

IT (TRIESTE) participant 209˙520.00
13    UNIVERSITA POLITECNICA DELLE MARCHE

 Organization address address: PIAZZA ROMA 22
city: ANCONA
postcode: 60121

contact info
Titolo: Dr.
Nome: Gianluca
Cognome: Svegliati Baroni
Email: send email
Telefono: +39 071 2206043
Fax: +39 071 2206044

IT (ANCONA) participant 207˙240.00
14    UNIVERSITY OF BRISTOL

 Organization address address: TYNDALL AVENUE SENATE HOUSE
city: BRISTOL
postcode: BS8 1TH

contact info
Titolo: Mr.
Nome: Vince
Cognome: Boyle
Email: send email
Telefono: +44 117 3317575
Fax: +44 117 9250900

UK (BRISTOL) participant 185˙776.00
15    UNIVERSITA DEGLI STUDI DI MODENA E REGGIO EMILIA

 Organization address address: VIA UNIVERSITA 4
city: MODENA
postcode: 41100

contact info
Titolo: Prof.
Nome: Paola
Cognome: Borella
Email: send email
Telefono: +39 320 6658960
Fax: +39 059 851762

IT (MODENA) participant 185˙594.00
16    Astellas Pharma Europe B.V

 Organization address address: Elisabethhof 1
city: Leiderdorp
postcode: 2353EW

contact info
Titolo: Dr.
Nome: Steve
Cognome: Van Os
Email: send email
Telefono: +31 71545 5536
Fax: +31 715 455219

NL (Leiderdorp) participant 35˙602.85
17    Medizinische Universitaet Graz

 Organization address address: AUENBRUGGERPLATZ 2
city: GRAZ
postcode: 8036

contact info
Titolo: Prof.
Nome: Michael
Cognome: Trauner
Email: send email
Telefono: +43 (0316) 385 81803
Fax: +43 (0316) 385 17108

AT (GRAZ) participant 0.00

Mappa


 Word cloud

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

diagnosis    epidemiological    related    liver    obesity    underlying    lifestyle    scientists    patients    biobanks    serious    fatty    disease    nash    alcoholic    clinical    inhibition    collaborative    prevent    mechanisms    histologically    mortality    genetic    serum    patient    nafld    establishment    practising    hepatologists    data    progression    flip    network    severe    therapy    diagnostic    foundations    pharmacological   

 Obiettivo del progetto (Objective)

'Non-alcoholic fatty liver disease (NAFLD) has become one of the top concerns for the practising hepatogastroenterologist due to the obesity epidemic and its potential to progress to advanced liver disease which significantly impacts on overall and liver-related mortality. The aim of the FLIP (Fatty Liver: Inhibition of Progression) project is to understand and prevent the progression of liver disease in NAFLD. FLIP is a consortium of basic scientists and practising clinical hepatologists with an established track record and focus on research into the underlying mechanisms and management of patients with NAFLD. Therefore FLIP provides a unique opportunity to assemble the largest European cohort of patients with histologically diagnosed NAFLD with clinical and epidemiological data and with biobanks of DNA, frozen liver tissue and serum. These will be used in a wide range of collaborative inter-disciplinary research projects aimed at addressing key unanswered questions related to the mechanisms and consequences of liver injury in NAFLD and the development of novel preventive and therapeutic strategies. The main outcomes of FLIP will be new insights in the progression of liver disease in NAFLD in terms of initiating mechanisms and patients at risk, innovative diagnostic methods particularly adapted for large-scale screening and prognostic evaluation, improved implementation of lifestyle changes, collaboration with leading biotechnological or pharmaceutical companies in order to translate to the market diagnostic tests or newly identified molecular targets for pharmacological therapy. By disseminating the project’s results, FLIP will further help the European Community to suggest guidelines on the management of this emerging liver disease. The long-term goal is to lay the foundations for the future of NAFLD research in Europe by creating a Collaborative Research Network on NAFLD that will continue the work initiated by the FLIP consortium.'

Introduzione (Teaser)

The increase in obesity over the years has alerted scientists to investigate one of its most serious adverse effects, non-alcoholic steatohepatitis (NASH).

Descrizione progetto (Article)

Fat deposition in the liver mainly due to obesity causes NASH that resembles alcoholic liver disease. In its most severe form, NASH can lead to liver failure and is a serious cause of liver-associated mortality.

The scope of the EU-funded 'Fatty liver: inhibition of progression' (http://www.flip-fp7.eu/ (FLIP)) project was to understand and prevent the progression of NASH. The consortium brought together leading scientists in the field and clinical hepatologists to study the underlying mechanisms of NASH development and improve patient management.

Among the biggest achievements of the project was the establishment of the largest European database of NASH patients. This includes clinical and epidemiological data as well as biobanks of patient samples. Analysis of this information enabled project partners to identify novel epidemiological and genetic determinants for NASH, both in adults and adolescents. The FLIP consortium performed the largest genetic studies in patients with histologically characterised NASH and identified robust genetic predictors of disease severity.

From a clinical perspective, the FLIP study generated a standardised histological classification that pathologists across Europe can use for diagnosis and staging of NASH. Through the discovery of new serum markers and non-invasive imaging tools, it hopes to improve disease diagnosis and prognosis.

To elucidate the events that drive the onset and progression of NASH, researchers developed a number of new animal models and in vitro culture systems. They unravelled various metabolic, inflammatory and fibrotic factors central for NASH initiation that could also serve as pharmacological targets.

Importantly, the FLIP study laid the foundations for future research in Europe in NASH through the establishment of a European Collaborative Research Network on NASH. Educating the public on the consequences of an unhealthy lifestyle and poor nutritional choices on the health of the liver should help reverse this devastating trend. Work on validation of pharmacological targets in NASH should help design effective drug therapy for the most severe patients.

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