METABASE

Metagenome and Bariatric Surgery - New Avenues to Treat Metabolic Disease

 Coordinatore GOETEBORGS UNIVERSITET 

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 Nazionalità Coordinatore Sweden [SE]
 Totale costo 2˙000˙000 €
 EC contributo 2˙000˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2013-CoG
 Funding Scheme ERC-CG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-11-01   -   2019-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    GOETEBORGS UNIVERSITET

 Organization address address: VASAPARKEN
city: GOETEBORG
postcode: 405 30

contact info
Titolo: Dr.
Nome: Ellen
Cognome: Rydberg
Email: send email
Telefono: +46 31 786 6470
Fax: +46 31 786 4355

SE (GOETEBORG) hostInstitution 2˙000˙000.00
2    GOETEBORGS UNIVERSITET

 Organization address address: VASAPARKEN
city: GOETEBORG
postcode: 405 30

contact info
Titolo: Dr.
Nome: Gert Fredrik
Cognome: Bäckhed
Email: send email
Telefono: +46 31 342 7833
Fax: +46 31 823 762

SE (GOETEBORG) hostInstitution 2˙000˙000.00

Mappa


 Word cloud

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germ    bariatric    altered    environmental    free    mice    metabolic    patients    surgical    mechanisms    diseases    beneficial    surgery    indicate    metabolism    gut    directly    determine    clinical    obesity    microbiota   

 Obiettivo del progetto (Objective)

'Obesity and associated metabolic diseases such as type 2 diabetes are increasing worldwide and are the result of complex gene-environment interactions. Recent studies indicate that socio-demographic and environmental factors are more important for disease development than genetics, and we and others have demonstrated that the gut microbiota can be considered an environmental factor that contributes to obesity. Effective treatment for obesity remains a challenge and bariatric surgery is the only available therapy that is proven to maintain weight loss. Intriguingly, bariatric surgery also improves glucose metabolism, but the underlying molecular mechanisms for this beneficial effect are unclear. An altered gut microbiota has been linked to metabolic diseases and pilot studies indicate that the gut microbiota is also altered upon bariatric surgery; these findings suggest that some of the improved metabolic features following bariatric surgery may be mediated by altered composition of the gut microbiota. The overall goal of this proposal is to integrate clinical research with mechanistic studies in mice to determine if and how the gut microbiota mediates the beneficial effects of bariatric surgery. We will define how bariatric surgery alters the gut metagenome in humans, both at a species and at a functional level. By transferring the fecal microbiota from these patients before and after surgery to germ-free mice, we will determine if an altered gut microbiota directly modulates host metabolism. Finally, we will establish surgical methods in germ-free mice to directly test whether the beneficial effects observed following surgery require a microbiota. Increased understanding of these mechanisms may provide the basis for non-surgical treatments based on supplementation of novel probiotics to treat metabolic diseases. Follow-up work in larger clinical cohorts may also indicate how patients can be stratified to determine who would benefit the most from bariatric surgery.'

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