Pediatric Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, the Netherlands; Section of Molecular Metabolism and Nutrition, Department of Pediatrics, University of Groningen, University Medical Center Groningen, the Netherlands.
Pediatric Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, the Netherlands.
J Cyst Fibros. 2019 May;18(3):313-320. doi: 10.1016/j.jcf.2018.08.009. Epub 2018 Sep 7.
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.
随着囊性纤维化(CF)肺部并发症治疗水平的提高,胃肠道问题在 CF 发病率中的重要性日益凸显。除了胰腺功能不全之外,CF 的胃肠道表型的一个标志是胆汁酸动态平衡的破坏。胆汁酸动态平衡对于包括脂肪吸收、炎症、微生物组成以及全身能量代谢调节在内的许多胃肠道过程都很重要。本文综述了 CF 中胆汁酸动态平衡的损害,及其对胃肠道和代谢并发症的可能影响,以及其作为治疗靶点的潜力。