Literature DB >> 14517804

Biliary diversion for progressive familial intrahepatic cholestasis: improved liver morphology and bile acid profile.

Amethyst C Kurbegov1, Kenneth D R Setchell, Joel E Haas, Gary W Mierau, Michael Narkewicz, John D Bancroft, Frederick Karrer, Ronald J Sokol.   

Abstract

BACKGROUND AND AIMS: Progressive familial intrahepatic cholestasis (PFIC) is characterized by pruritus, intrahepatic cholestasis, low serum gamma-glutamyltransferase levels, and characteristic "Byler bile" on electron microscopy. Many patients require liver transplantation, but partial external biliary diversion (PEBD) has shown therapeutic promise. However, the effect of PEBD on liver morphology and bile composition has not been evaluated.
METHODS: We reviewed liver biopsy specimens from 3 children with low gamma-glutamyltransferase PFIC before and after PEBD. Follow-up liver biopsies were performed 9-60 months after PEBD. Light and electron microscopic features were scored blindly. Biliary bile acid composition was analyzed by gas chromatography-mass spectrometry before and after PEBD in 1 patient and after PEBD in 2 patients.
RESULTS: Following PEBD, all patients improved clinically. Preoperative biopsy specimens showed characteristic features of PFIC, including portal fibrosis, chronic inflammation, cholestasis, giant cell transformation, and central venous mural sclerosis. Ultrastructural findings included coarse, granular canalicular Byler bile, effaced canalicular microvilli, and proliferative pericanalicular microfilaments. Following diversion, histology showed almost complete resolution of cholestasis, portal fibrosis, and inflammation with resolution of ultrastructural abnormalities. Biliary bile acids before PEBD consisted predominantly of cholic acid. After PEBD, the proportion of chenodeoxycholic acid increased significantly in 1 patient and was above the PFIC range in a second patient.
CONCLUSIONS: The resolution of hepatic morphologic abnormalities following PEBD supports PEBD as an effective therapy for PFIC. The improved biliary bile acid composition suggests enhanced bile acid secretion after PEBD, perhaps by induction of alternative canalicular transport proteins.

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Year:  2003        PMID: 14517804     DOI: 10.1016/s0016-5085(03)01199-5

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  25 in total

Review 1.  Liver transplantation and the management of progressive familial intrahepatic cholestasis in children.

Authors:  Ashley Mehl; Humberto Bohorquez; Maria-Stella Serrano; Gretchen Galliano; Trevor W Reichman
Journal:  World J Transplant       Date:  2016-06-24

2.  Outcome of partial internal biliary diversion for intractable pruritus in children with cholestatic liver disease.

Authors:  P Ramachandran; N P Shanmugam; S Al Sinani; V Shanmugam; S Srinivas; M Sathiyasekaran; V Tamilvanan; M Rela
Journal:  Pediatr Surg Int       Date:  2014-07-27       Impact factor: 1.827

3.  Quantitative metabolomics comparison of traditional blood draws and TAP capillary blood collection.

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Review 4.  [Biliary atresia and congenital cholestatic syndromes : Characteristics before, after and during transition].

Authors:  N Junge; J Dingemann; C Petersen; M P Manns; N Richter; J Klempnauer; U Baumann; A Schneider
Journal:  Internist (Berl)       Date:  2018-11       Impact factor: 0.743

Review 5.  Autoimmune BSEP disease: disease recurrence after liver transplantation for progressive familial intrahepatic cholestasis.

Authors:  Ralf Kubitz; Carola Dröge; Stefanie Kluge; Claudia Stross; Nathalie Walter; Verena Keitel; Dieter Häussinger; Jan Stindt
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6.  Combined deletion of Fxr and Shp in mice induces Cyp17a1 and results in juvenile onset cholestasis.

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7.  Bile acid pool dynamics in progressive familial intrahepatic cholestasis with partial external bile diversion.

Authors:  Hilary S Jericho; Elizabeth Kaurs; Renze Boverhof; Alex Knisely; Benjamin L Shneider; Henkjan J Verkade; Peter F Whitington
Journal:  J Pediatr Gastroenterol Nutr       Date:  2015-03       Impact factor: 2.839

Review 8.  Partial external biliary diversion for the treatment of intractable pruritus in children with progressive familial intrahepatic cholestasis: report of two cases.

Authors:  Saniye Ekinci; Ibrahim Karnak; Figen Gürakan; Aysel Yüce; Mehmet Emin Senocak; F Cahit Tanyel; Nebil Büyükpamukçu
Journal:  Surg Today       Date:  2008-07-31       Impact factor: 2.549

Review 9.  Congenital cholestatic syndromes: what happens when children grow up?

Authors:  S C Ling
Journal:  Can J Gastroenterol       Date:  2007-11       Impact factor: 3.522

10.  Activity of the bile salt export pump (ABCB11) is critically dependent on canalicular membrane cholesterol content.

Authors:  Coen C Paulusma; D Rudi de Waart; Cindy Kunne; Kam S Mok; Ronald P J Oude Elferink
Journal:  J Biol Chem       Date:  2009-02-19       Impact factor: 5.157

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