BrainGutAnalytics · Multiomics based analysis of brain-gut axis: A search for gastrointestinal disease phenotypes
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2020-10-01 → 2022-09-30
- EU contribution
- €214,159
- Participants
- 1
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
Multiomics based analysis of brain-gut axis: A search for gastrointestinal disease phenotypes
Irritable Bowel Syndrome (IBS) is a well-known gastrointestinal disorder, which affects about 10% of global human population. IBS alters bowel habits of affected patients by means of diarrhoea, constipation, or a mix of both of these conditions. This is often accompanied by unexplained abdominal pain, fatigue and aggravated food sensitivities, which together significantly deteriorate the quality of life of a patient with IBS. Traditionally, IBS is thought to be a functional gastrointestinal disorder as its origin was associated with the dysfunction of gut related variables e.g. intestinal motility, transit time and motor complexes. However, the recent scientific literature instead describes IBS as a consequence of dysfunction of Brain-Gut-Microbiota (BGM) axis. The BGM axis is a relatively new but rapidly emerging theory in the field of medicine and gastrointestinal health, which refers to the presence of an intricate and bi-directional relationship between human gut and brain. This nexus is thought to be modulated by the diverse colonies of gut microbiome through neuronal signalling, immune system and systemic circulation channels. A disruption in BGM axis is hypothesised as an underlying cause of various previously unexplained psychological as well as gastrointestinal disorders, such as IBS. As the exact aetiology of IBS is unknown, a clear differential diagnosis test that can identify IBS in patients does not yet exists. Instead, IBS is often termed as a ‘diagnosis of exclusion’ as various other overlapping gastrointestinal disorders first need to be ruled out before IBS can be determined. The additional diagnostic testing significantly increases physical and emotional suffering for the patients as a clear diagnosis for IBS is a starting point to receive an effective treatment. This also causes additional burden and financial strain on national health system as the clinicians and gastroenterologists who work with IBS cases on a day to day basis are obliged to spend more time and resources for diagnosing IBS compared to other gastrointestinal disorders. This Marie Skłodowska Curie (MSC) Individual Fellowship action entitled "Multiomics based analysis of brain-gut axis: A search for gastrointestinal disease phenotypes” and abbreviated as BrainGutAnalytics, aims to study brain-gut axis and associated irritable bowel syndrome by employing advanced data science, machine learning and statistical analysis techniques. The keys aim of this research is to search for novel, exclusive and generalisable digital phenotypes of IBS from multiomics datasets, which can be used as reliable biomarkers for IBS. The secondary aim of this work is to translate these biomarkers into a novel test for IBS diagnosis, which can be applied in regular clinical practice.
Data: CORDIS, © European Union
Project 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.
Original text from CORDIS.
Participants
- HELSE BERGEN HF · BergenCoordinatorNorway
Links
Data: CORDIS, © European Union
