Phenotype and Clinical Course of Inflammatory Bowel Disease With Co-existent Celiac Disease

被引:18
作者
Tse, Chung Sang [1 ]
Deepak, Parakkal [2 ,3 ]
De La Fuente, Jaime [1 ]
Bledsoe, Adam C. [2 ]
Larson, Joseph J. [2 ]
Murray, Joseph A. [2 ]
Papadakis, Konstantinos A. [2 ]
机构
[1] Mayo Clin, Dept Internal Med, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[3] Washington Univ, Sch Med, Div Gastroenterol, John T Milliken Dept Med, St Louis, MO 63110 USA
关键词
Inflammatory bowel disease; celiac disease; primary sclerosing cholangitis; clinical course; concurrent immune-mediated gastrointestinal diseases; PRIMARY SCLEROSING CHOLANGITIS; VITAMIN-D-RECEPTOR; ULCERATIVE-COLITIS; BILIARY EPITHELIUM; CROHNS-DISEASE; UNITED-STATES; D DEFICIENCY; T-CELLS; PREVALENCE; RISK;
D O I
10.1093/ecco-jcc/jjy061
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Inflammatory bowel diseases, principally Crohn's disease and ulcerative colitis, and celiac disease are among the most common immune-mediated gastrointestinal diseases. We aim to elucidate the clinical course and outcomes of patients with concomitant inflammatory bowel disease and celiac disease, a unique population that remains scarcely studied to date. Methods: A retrospective matched case-control study of adults with co-existent inflammatory bowel disease [IBD] and celiac disease was performed at a tertiary referral institution in North America. Logistic regression and Kaplan-Meier curves compared disease characteristics and clinical outcomes of the two groups. Results: A total of 342 inflammatory bowel disease patients were included in this study, of whom 114 had co-existent celiac disease and 228 did not. Patients with co-existent inflammatory bowel disease and celiac disease had higher rates of primary sclerosing cholangitis [19.3% vs 5.7%; odds ratio, 4.4; 95% confidence interval, 2.1-9.4; p < 0.001], extensive ulcerative colitis [78.1% vs 59.0%; odds ratio, 2.8; 95% confidence interval, 1.5-5.5; p = 0.002], and family history of celiac disease [10.5% vs 3.5%; odds ratio 3.2; 95% confidence interval, 1.3-8.2; p = 0.01], compared with patients without concomitant celiac disease. Conclusions: Patients with inflammatory bowel disease with concomitant celiac disease have unique phenotypic features compared with non-celiac inflammatory bowel disease, with higher risks for colitis-related hospitalisations, extensive colitis, and primary sclerosing cholangitis. Increased recognition of co-existent IBD and celiac disease can prompt clinicians to investigate for concomitant disease sooner, particularly in patients with seemingly refractory disease.
引用
收藏
页码:973 / 980
页数:8
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