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Multiomics based analysis of brain-gut axis: A search for gastrointestinal disease phenotypes

Project description

Insight into the brain–gut axis

Emerging evidence indicates a reciprocal interaction between the gut and the brain, with gastrointestinal disorders presenting with various brain alterations and vice versa. Scientists of the EU-funded BrainGutAnalytics project aim to obtain a deeper understanding of the nature and operation of this gut–brain axis. Using a multiomics approach that combines neuroimaging, clinical diagnostics and microbial profiling, they will identify suitable gastrointestinal phenotypes and correlate them with biomarkers. These biomarkers will form the basis for a new diagnostic system as well as for the design of drugs and precision treatment for both neurological and gastrointestinal disorders.

Objective

An intimate yet less known relation between human brain and gut is rapidly emerging as several recent studies have identified various alterations within brain as a result of gastrointestinal disorders and reported comparable variations in gastrointestinal system due to altered brain outputs. These relationships are collectively termed as brain-gut axis and a deeper understanding of its exact nature and operation can lead to development of novel diagnosis, drugs and precision treatment for both neurological and gastrointestinal disorders.

The first step towards establishing a comprehensive understanding of brain-gut axis is to identify suitable phenotypes that can be used to describe certain disease state and serve as basis for further investigations into operation of brain-gut axis. In this study, a multiomics based data analysis approach is proposed to search for exclusive and generalizable phenotypes of a certain gastrointestinal disorder. Our multiomics data consist of multimodal imagery of brain and gut, clinical diagnostics, microbial profiling, questionnaire based disease evaluations, genetic and molecular representations taken from carefully designed cohorts of patients and healthy controls. Our data analyses will employ a variety of techniques including digital image processing, computer vision, machine learning and statistical methods to determine covariate factors in omics, which will be then used to identify representative biomarkers for gastrointestinal disorders.

We also aim to develop a novel diagnosis system for gastrointestinal disease based on novel biomarkers through a combination of neuroimaging and digital image processing pipeline . Our research is expected to excel the existing knowledge on brain-gut axis by exposing critical phenotypes, employing them for early diagnostic and paving way towards deeper understanding of brain-gut axis.

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

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(opens in new window) H2020-MSCA-IF-2019

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Coordinator

HELSE BERGEN HF
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 214 158,72
Address
HAUKELANDSVEIEN 22
5021 BERGEN
Norway

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Region
Norge Vestlandet Vestland
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 214 158,72
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