Immune-mediated diseases in primary sclerosing cholangitis

被引:39
|
作者
Lamberts, Laetitia E. [1 ]
Janse, Marcel [1 ]
Haagsma, Elizabeth B. [1 ]
van den Berg, Arie P. [1 ]
Weersma, Rinse K. [1 ]
机构
[1] Univ Groningen, Dept Gastroenterol & Hepatol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
关键词
Autoimmune disease; Cholestatic liver disease; AUTOIMMUNE HEPATITIS; ULCERATIVE-COLITIS; NATURAL-HISTORY; PROGNOSTIC VARIABLES; OVERLAP SYNDROMES; SARCOIDOSIS; PREVALENCE; ASSOCIATION; DIAGNOSIS; FEATURES;
D O I
10.1016/j.dld.2011.05.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Primary sclerosing cholangitis is a chronic cholestatic liver disease. An immune aetiology is suggested by associations between PSC and inflammatory bowel disease. Data on concomitant prevalence of other immune-mediated diseases is limited. Aim: To assess the prevalence of concomitant immune-mediated diseases and the impact on disease outcome in PSC. Methods: We included 241 patients and retrospectively reviewed medical charts. Results: Altogether 172(71.4%) patients had concomitant immune-mediated disease, including IBD (149, 61.8%), autoimmune hepatitis (15, 6.2%) and other immune-mediated diseases (47, 19.5%). Thirty nine patients (22.7%) had more than one immune-mediated disease other than PSC. Most frequent extrahepatic non-IBD immune-mediated diseases were sarcoidosis, thyroid disease, and type 1 diabetes mellitus. Age at PSC diagnosis was lower in patients with IBD. In patients with other immune-mediated diseases than autoimmune hepatitis or IBD, age at PSC diagnosis was higher. Younger age at diagnosis and concomitant IBD related to longer survival till death or liver transplantation. Conclusions: In a large PSC population, a high prevalence of concomitant immune-mediated diseases was found. IBD occurred more often in early-acquired PSC, and the other immune-mediated diseases more often in later-acquired PSC. No effect on outcome was found for non-IBD immune mediated disease. (C) 2011 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:802 / 806
页数:5
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