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dc.contributor.authorBerentsen, Birgitte
dc.contributor.authorNagaraja, Bharath Halandur
dc.contributor.authorTeige, Erica Persson
dc.contributor.authorLied, Gülen Arslan
dc.contributor.authorLundervold, Astri
dc.contributor.authorLundervold, Katarina
dc.contributor.authorSteinsvik, Elisabeth Kjelsvik
dc.contributor.authorHillestad, Eline Margrete Randulff
dc.contributor.authorValeur, Jørgen
dc.contributor.authorBrønstad, Ingeborg
dc.contributor.authorGilja, Odd Helge
dc.contributor.authorOsnes, Berge
dc.contributor.authorHatlebakk, Jan Gunnar
dc.contributor.authorHaász, Judit
dc.contributor.authorLabus, Jennifer
dc.contributor.authorGupta, Arpana
dc.contributor.authorMayer, Emeran
dc.contributor.authorBenitez-Páez, Alfonso
dc.contributor.authorSanz, Yolanda
dc.contributor.authorLundervold, Arvid
dc.contributor.authorHausken, Trygve
dc.date.accessioned2021-02-12T08:19:48Z
dc.date.available2021-02-12T08:19:48Z
dc.date.created2020-09-11T23:20:50Z
dc.date.issued2020-09
dc.PublishedMedicine. 2020, 99:e21950 (37), 1-8.
dc.identifier.issn0025-7974
dc.identifier.urihttps://hdl.handle.net/11250/2727593
dc.description.abstractIntroduction: Irritable bowel syndrome (IBS) is a common clinical label for medically unexplained gastrointestinal (GI) symptoms, recently described as a disturbance of the brain-gut-microbiota (BGM) axis. To gain a better understanding of the mechanisms underlying the poorly understood etiology of IBS, we have designed a multifaceted study that aim to stratify the complex interaction and dysfunction between the brain, the gut, and the microbiota in patients with IBS. Methods: Deep phenotyping data from patients with IBS (n = 100) and healthy age- (between 18 and 65) and gender-matched controls (n = 40) will be collected between May 2019 and December 2021. Psychometric tests, questionnaires, human biological tissue/samples (blood, faeces, saliva, and GI biopsies from antrum, duodenum, and sigmoid colon), assessment of gastric accommodation and emptying using transabdominal ultrasound, vagal activity, and functional and structural magnetic resonance imaging (MRI) of the brain, are included in the investigation of each participant. A subgroup of 60 patients with IBS-D will be further included in a 12-week low FODMAP dietary intervention-study to determine short and long-term effects of diet on GI symptoms, microbiota composition and functions, molecular GI signatures, cognitive, emotional and social functions, and structural and functional brain signatures. Deep machine learning, prediction tools, and big data analyses will be used for multivariate analyses allowing disease stratification and diagnostic biomarker detection. Discussion: To our knowledge, this is the first study to employ unsupervised machine learning techniques and incorporate systems-based interactions between the central and the peripheral components of the brain-gut-microbiota axis at the levels of the multiomics, microbiota profiles, and brain connectome of a cohort of 100 patients with IBS and matched controls; study long-term safety and efficacy of the low-FODMAP diet on changes in nutritional status, gut microbiota composition, and metabolites; and to investigate changes in the brain and gut connectome after 12 weeks strict low-FODMAP-diet in patients with IBS. However, there are also limitations to the study. As a restrictive diet, the low-FODMAP diet carries risks of nutritional inadequacy and may foster disordered eating patterns. Strict FODMAP restriction induces a potentially unfavourable gut microbiota, although the health effects are unknown.en_US
dc.language.isoengen_US
dc.publisherWolters Kluwer Healthen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleStudy protocol of the Bergen brain-gut-microbiota-axis study: A prospective case-report characterization and dietary intervention study to evaluate the effects of microbiota alterations on cognition and anatomical and functional brain connectivity in patients with irritable bowel syndromeen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s)en_US
dc.source.articlenumberp e21950en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1097/MD.0000000000021950
dc.identifier.cristin1829311
dc.source.journalMedicineen_US
dc.source.4099:e21950
dc.source.1437
dc.source.pagenumber1-8en_US
dc.source.volume99en_US
dc.source.issue37en_US


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