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Bile acid analysis in human disorders of bile acid biosynthesis
- Source :
- Molecular Aspects of Medicine. 56:10-24
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Bile acids facilitate the absorption of lipids in the gut, but are also needed to maintain cholesterol homeostasis, induce bile flow, excrete toxic substances and regulate energy metabolism by acting as signaling molecules. Bile acid biosynthesis is a complex process distributed across many cellular organelles and requires at least 17 enzymes in addition to different metabolite transport proteins to synthesize the two primary bile acids, cholic acid and chenodeoxycholic acid. Disorders of bile acid synthesis can present from the neonatal period to adulthood and have very diverse clinical symptoms ranging from cholestatic liver disease to neuropsychiatric symptoms and spastic paraplegias. This review describes the different bile acid synthesis pathways followed by a summary of the current knowledge on hereditary disorders of human bile acid biosynthesis with a special focus on diagnostic bile acid profiling using mass spectrometry. (C) 2017 Elsevier Ltd. All rights reserved
- Subjects :
- Adult
0301 basic medicine
medicine.drug_class
Metabolite
Clinical Biochemistry
Cholic Acid
Biology
Chenodeoxycholic Acid
digestive system
Biochemistry
Mass Spectrometry
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Biosynthesis
Chenodeoxycholic acid
Enterohepatic Circulation
CYP27A1
BAAT
medicine
Animals
Homeostasis
Humans
Intestinal Mucosa
Zellweger Syndrome
Molecular Biology
Cholestasis
Bile acid
Spastic Paraplegia, Hereditary
Cholic acid
Infant
General Medicine
Intestines
Cholesterol
030104 developmental biology
Liver
chemistry
Molecular Medicine
CYP8B1
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 00982997
- Volume :
- 56
- Database :
- OpenAIRE
- Journal :
- Molecular Aspects of Medicine
- Accession number :
- edsair.doi.dedup.....40d4b7765e2f891068228e549525c6ce
- Full Text :
- https://doi.org/10.1016/j.mam.2017.03.003