Literature DB >> 35322291

Portal plate bile duct diameter in biliary atresia is associated with long-term outcome.

Michael Shpoliansky1,2, Ana Tobar3,4, Yael Mozer-Glassberg5,3, Michal Rosenfeld Bar-Lev5,3, Raanan Shamir5,3, Michal Shafir5, Michael Gurevich3,6, Orith Waisbourd-Zinman5,3.   

Abstract

PURPOSE: Kasai portoenterostomy (KPE) is the only treatment currently available for biliary atresia (BA). Age at KPE and surgical experience are prognostic factors for a successful KPE. Here, we aimed to assess whether the size of bile ductules at the porta hepatis during KPE correlates with KPE success and transplant-free survival (TFS).
METHODS: A retrospective analysis of patients diagnosed with BA during 2000-2019. Porta hepatis biopsies were reviewed for diameters of five representative ducts, and a mean ductal diameter (MDD) was calculated. Laboratory values including pre- and postoperative bilirubin levels were analyzed.
RESULTS: The cohort included 77 patients; for 33, ductal plate biopsy was available. KPE was successful in six of eight patients with MDD ≥ 50 µm, and in five of 25 with MDD < 50 µm, p = 0.008, OR = 12.0 (95% CI 1.83-78.3). Ten-year survival with native liver was higher in patients with MDD ≥ 50 µm than in patients with MDD < 50 µm, p < 0.001, HR 0.038 (95% CI 0.007-0.207). Direct bilirubin < 1 mg/dl 3 months post-KPE was associated with improved 2-year post-KPE TFS (27.7% vs. 13.9%, p < 0.0001).
CONCLUSIONS: MDD ≥ 50 µm correlates with KPE success and a higher rate of TFS. Direct bilirubin < 1 mg/dl 3 months post-operation may serve as a marker of successful biliary excretion, and a predictor of 2-year TFS.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Bile duct; Biliary atresia; Kasai portoenterostomy; Native liver; Survival

Mesh:

Substances:

Year:  2022        PMID: 35322291     DOI: 10.1007/s00383-022-05113-2

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  36 in total

1.  Cytomegalovirus-associated biliary atresia: An aetiological and prognostic subgroup.

Authors:  Augusto Zani; Alberto Quaglia; Nedim Hadzić; Mark Zuckerman; Mark Davenport
Journal:  J Pediatr Surg       Date:  2015-03-07       Impact factor: 2.545

2.  The dendritic cell-T helper 17-macrophage axis controls cholangiocyte injury and disease progression in murine and human biliary atresia.

Authors:  Celine S Lages; Julia Simmons; Avery Maddox; Keaton Jones; Rebekah Karns; Rachel Sheridan; Shiva Kumar Shanmukhappa; Sujit Mohanty; Matthew Kofron; Pierre Russo; Yui-Hsi Wang; Claire Chougnet; Alexander G Miethke
Journal:  Hepatology       Date:  2016-11-10       Impact factor: 17.425

3.  CFC1 gene involvement in biliary atresia with polysplenia syndrome.

Authors:  Anne Davit-Spraul; Christiane Baussan; Bogdan Hermeziu; Olivier Bernard; Emmanuel Jacquemin
Journal:  J Pediatr Gastroenterol Nutr       Date:  2008-01       Impact factor: 2.839

4.  Congenital biliary atresia and jaundice in lambs and calves.

Authors:  P Harper; J W Plant; D B Unger
Journal:  Aust Vet J       Date:  1990-01       Impact factor: 1.281

5.  The epidemiology of extrahepatic biliary atresia in New York State, 1983-98.

Authors:  Alissa R Caton; Charlotte M Druschel; Louise A McNutt
Journal:  Paediatr Perinat Epidemiol       Date:  2004-03       Impact factor: 3.980

Review 6.  Biliary Atresia: Clinical and Research Challenges for the Twenty-First Century.

Authors:  Jorge A Bezerra; Rebecca G Wells; Cara L Mack; Saul J Karpen; Jay H Hoofnagle; Edward Doo; Ronald J Sokol
Journal:  Hepatology       Date:  2018-09       Impact factor: 17.425

7.  Maternal microchimerism in underlying pathogenesis of biliary atresia: quantification and phenotypes of maternal cells in the liver.

Authors:  Toshihiro Muraji; Naoki Hosaka; Naoki Irie; Makiko Yoshida; Yukihiro Imai; Kohichi Tanaka; Yasutsugu Takada; Seisuke Sakamoto; Hironori Haga; Susumu Ikehara
Journal:  Pediatrics       Date:  2008-03       Impact factor: 7.124

8.  Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome.

Authors:  John-Paul Berauer; Anya I Mezina; David T Okou; Aniko Sabo; Donna M Muzny; Richard A Gibbs; Madhuri R Hegde; Pankaj Chopra; David J Cutler; David H Perlmutter; Laura N Bull; Richard J Thompson; Kathleen M Loomes; Nancy B Spinner; Ramakrishnan Rajagopalan; Stephen L Guthery; Barry Moore; Mark Yandell; Sanjiv Harpavat; John C Magee; Binita M Kamath; Jean P Molleston; Jorge A Bezerra; Karen F Murray; Estella M Alonso; Philip Rosenthal; Robert H Squires; Kasper S Wang; Milton J Finegold; Pierre Russo; Averell H Sherker; Ronald J Sokol; Saul J Karpen
Journal:  Hepatology       Date:  2019-03-21       Impact factor: 17.425

9.  The toxin biliatresone causes mouse extrahepatic cholangiocyte damage and fibrosis through decreased glutathione and SOX17.

Authors:  Orith Waisbourd-Zinman; Hong Koh; Shannon Tsai; Pierre-Marie Lavrut; Christine Dang; Xiao Zhao; Michael Pack; Jeff Cave; Mark Hawes; Kyung A Koo; John R Porter; Rebecca G Wells
Journal:  Hepatology       Date:  2016-05-20       Impact factor: 17.425

10.  A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.

Authors:  Ying Chen; Melissa A Gilbert; Christopher M Grochowski; Deborah McEldrew; Jessica Llewellyn; Orith Waisbourd-Zinman; Hakon Hakonarson; Joan E Bailey-Wilson; Pierre Russo; Rebecca G Wells; Kathleen M Loomes; Nancy B Spinner; Marcella Devoto
Journal:  PLoS Genet       Date:  2018-08-13       Impact factor: 5.917

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