Literature DB >> 18222442

Immunoglobulin G4-associated cholangitis: clinical profile and response to therapy.

Amaar Ghazale1, Suresh T Chari, Lizhi Zhang, Thomas C Smyrk, Naoki Takahashi, Michael J Levy, Mark D Topazian, Jonathan E Clain, Randall K Pearson, Bret T Petersen, Santhi Swaroop Vege, Keith Lindor, Michael B Farnell.   

Abstract

BACKGROUND & AIMS: Immunoglobulin (Ig)G4-associated cholangitis (IAC) is the biliary manifestation of a steroid-responsive multisystem fibroinflammatory disorder in which affected organs have a characteristic lymphoplasmacytic infiltrate rich in IgG4-positive cells. We describe clinical features, treatment response, and predictors of relapse in IAC and compare relapse rates in IAC with intrapancreatic vs proximal bile duct strictures.
METHODS: We reviewed clinical, serologic, and imaging characteristics and treatment response in 53 IAC patients.
RESULTS: IAC patients generally were older (mean age, 62 y) men (85%), presenting with obstructive jaundice (77%) associated with autoimmune pancreatitis (92%), increased serum IgG4 levels (74%), and abundant IgG4-positive cells in bile duct biopsy specimens (88%). At presentation, biliary strictures were confined to the intrapancreatic bile duct in 51%; the proximal extrahepatic/intrahepatic ducts were involved in 49%. Initial presentation was treated with steroids (n = 30; median follow-up period, 29.5 months), surgical resection (n = 18; median follow-up period, 58 months), or was conservative (n = 5; median follow-up period, 35 months). Relapses occurred in 53% after steroid withdrawal; 44% relapsed after surgery and were treated with steroids. The presence of proximal extrahepatic/intrahepatic strictures was predictive of relapse. Steroid therapy normalized liver enzyme levels in 61%; biliary stents could be removed in 17 of 18 patients. Fifteen patients treated with steroids for relapse after steroid withdrawal responded; 7 patients on additional immunomodulatory drugs remain in steroid-free remission (median follow-up period, 6 months).
CONCLUSIONS: IAC should be suspected in unexplained biliary strictures associated with increased serum IgG4 and unexplained pancreatic disease. Relapses are common after steroid withdrawal, especially with proximal strictures. The role of immunomodulatory drugs for relapses needs further study.

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Year:  2007        PMID: 18222442     DOI: 10.1053/j.gastro.2007.12.009

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


  209 in total

1.  Diagnostic criteria for IgG4-related sclerosing cholangitis based on cholangiographic classification.

Authors:  Takahiro Nakazawa; Itaru Naitoh; Kazuki Hayashi; Fumihiro Okumura; Katsuyuki Miyabe; Michihiro Yoshida; Hiroaki Yamashita; Hirotaka Ohara; Takashi Joh
Journal:  J Gastroenterol       Date:  2011-09-23       Impact factor: 7.527

Review 2.  The Clinical and Pathological Features of IgG(4)-Related Disease.

Authors:  Arezou Khosroshahi; Vikram Deshpande; John H Stone
Journal:  Curr Rheumatol Rep       Date:  2011-12       Impact factor: 4.592

3.  Recommendations for the nomenclature of IgG4-related disease and its individual organ system manifestations.

Authors:  John H Stone; Arezou Khosroshahi; Vikram Deshpande; John K C Chan; J Godfrey Heathcote; Rob Aalberse; Atsushi Azumi; Donald B Bloch; William R Brugge; Mollie N Carruthers; Wah Cheuk; Lynn Cornell; Carlos Fernandez-Del Castillo; Judith A Ferry; David Forcione; Günter Klöppel; Daniel L Hamilos; Terumi Kamisawa; Satomi Kasashima; Shigeyuki Kawa; Mitsuhiro Kawano; Yasufumi Masaki; Kenji Notohara; Kazuichi Okazaki; Ji Kon Ryu; Takako Saeki; Dushyant Sahani; Yasuharu Sato; Thomas Smyrk; James R Stone; Masayuki Takahira; Hisanori Umehara; George Webster; Motohisa Yamamoto; Eunhee Yi; Tadashi Yoshino; Giuseppe Zamboni; Yoh Zen; Suresh Chari
Journal:  Arthritis Rheum       Date:  2012-10

Review 4.  Autoimmune pancreatitis and IgG4-related sclerosing disease.

Authors:  Terumi Kamisawa; Kensuke Takuma; Naoto Egawa; Koji Tsuruta; Tsuneo Sasaki
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2010-06-15       Impact factor: 46.802

Review 5.  Autoimmune pancreatitis and IgG4-related systemic diseases.

Authors:  Lizhi Zhang; Thomas C Smyrk
Journal:  Int J Clin Exp Pathol       Date:  2010-05-25

6.  High-dose ursodeoxycholic acid increases risk of adverse outcomes in patients with early stage primary sclerosing cholangitis.

Authors:  M H Imam; E Sinakos; A A Gossard; K V Kowdley; V A C Luketic; M Edwyn Harrison; T McCashland; A S Befeler; D Harnois; R Jorgensen; J Petz; J Keach; A C DeCook; F Enders; K D Lindor
Journal:  Aliment Pharmacol Ther       Date:  2011-09-29       Impact factor: 8.171

Review 7.  Treatment of IgG4-related disease : Current and future approaches.

Authors:  C A Perugino; J H Stone
Journal:  Z Rheumatol       Date:  2016-09       Impact factor: 1.372

Review 8.  Diagnosis of IgG4-related sclerosing cholangitis.

Authors:  Takahiro Nakazawa; Itaru Naitoh; Kazuki Hayashi; Katsuyuki Miyabe; Shuya Simizu; Takashi Joh
Journal:  World J Gastroenterol       Date:  2013-11-21       Impact factor: 5.742

Review 9.  Retroperitoneal fibrosis associated with immunoglobulin G4-related disease.

Authors:  Nao Fujimori; Tetsuhide Ito; Hisato Igarashi; Takamasa Oono; Taichi Nakamura; Yusuke Niina; Masayuki Hijioka; Lingaku Lee; Masahiko Uchida; Ryoichi Takayanagi
Journal:  World J Gastroenterol       Date:  2013-01-07       Impact factor: 5.742

10.  Autoimmune Pancreatitis.

Authors:  Gyanprakash A Ketwaroo; Sunil Sheth
Journal:  Gastroenterol Rep       Date:  2013-04-04       Impact factor: 3.651

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