医学
炎症性肠病
精确检验
内科学
胃肠病学
自身免疫性胰腺炎
人口
胰腺炎
自身免疫性肝炎
酒精性肝病
溃疡性结肠炎
肝炎
免疫学
疾病
环境卫生
肝硬化
作者
Michael Hirth,Christel Weiß,Philip Weidner,Christoph Antoni,A Thomann,Wolfgang Reindl,Matthias P. Ebert,Roland H. Pfützer,Alexander Schneider
出处
期刊:Zeitschrift Fur Gastroenterologie
[Georg Thieme Verlag KG]
日期:2018-05-01
卷期号:56 (05): 469-478
被引量:9
标识
DOI:10.1055/s-0043-123881
摘要
Abstract Objectives Patients with inflammatory bowel disease (IBD) frequently reveal features of pancreatic inflammation. However, the prevalence of IBD in patients with alcoholic pancreatitis (AP) and nonalcoholic pancreatitis (NAP) has not yet been determined, and the prevalence of IBD in patients with autoimmune pancreatitis (AiP) from Germany is unknown. Aims Thus, we aimed, first, to determine the prevalence of IBD in AP, NAP, and AiP from a tertiary center in Germany and, second, to characterize patients with AiP and IBD. Methods We performed a retrospective cross-sectional study to determine the prevalence of IBD in patients with different forms of pancreatitis presenting to our clinic. Results Compared to the general population and to a control group with viral hepatitis from our clinic, we observed the most significant increase of IBD in patients with AiP (n = 3/28; p < 0.0001 vs. general population, binomial proportion test; p = 0.0112 vs. hepatitis group, Fisher’s exact test), followed by a significant increase in subjects with NAP (n = 11/278; p < 0.0001 vs. general population, binomial proportion test; p = 0.0338 vs. hepatitis group, Fisher’s exact test). A review of previous studies on the prevalence of IBD among patients with AiP revealed a combined prevalence of 12 % (n = 43/355). Type 2 AiP is significantly more often associated with IBD than type 1 AiP (n = 28/48, 58 % vs. n = 7/129, 5 %; combined patient cohort, p < 10E − 12; Fisher’s exact test). Conclusions Immune-mediated mechanisms related to IBD may participate in the development of AiP, especially AiP type 2, and may also increase the risk for the development of other forms of pancreatic inflammation.
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