Bile acid homeostasis in gastrointestinal and metabolic complications of cystic fibrosis

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    Abstract

    With the improved treatment of the pulmonary complications of cystic fibrosis (CF), gastrointestinal problems have become more important in the morbidity in CF. A hallmark of the gastrointestinal phenotype of CF, apart from pancreatic insufficiency, is a disruption of bile acid homeostasis. Bile acid homeostasis is important for many gastrointestinal processes including fat absorption, inflammation, microbial composition, as well as regulation of whole body energy metabolism. This review describes the impairment of bile acid homeostasis in CF, its possible consequences for gastrointestinal and metabolic complications and its potential as a target for therapy. (C) 2018 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

    Original languageEnglish
    Pages (from-to)313-320
    Number of pages8
    JournalJournal of Cystic Fibrosis
    Volume18
    Issue number3
    DOIs
    Publication statusPublished - May-2019

    Keywords

    • Cystic fibrosis
    • Bile acids
    • Metabolism
    • Intestine
    • Liver
    • FARNESOID-X-RECEPTOR
    • TRANSMEMBRANE CONDUCTANCE REGULATOR
    • BETA-MURICHOLIC ACID
    • GROWTH-FACTOR 15
    • URSODEOXYCHOLIC ACID
    • GUT MICROBIOTA
    • LIVER-DISEASE
    • SUPPLEMENTATION IMPROVES
    • INTESTINAL-OBSTRUCTION
    • HEPATOBILIARY DISEASE

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