Similar subclinical enthesitis in celiac and inflammatory bowel diseases by ultrasound suggests a gut enthesis axis independent of spondyloarthropathy spectrum

• Published in: Rheumatology (Oxford, England) England), 2018-08, Vol.57 (8), p.1417-1422
• Main Authors: Bakirci Ureyen, Sibel, Karacaer, Cengiz, Toka, Bilal, Erturk, Zeynep, Eminler, Ahmet Tarik, Kaya, Muhammed, Tascilar, Koray, Tamer, Ali, Uslan, Ihsan, Kurum, Esra, McGonagle, Dennis, Aydin, Sibel Zehra
• Format: Article
• Language: English
• Subjects: Adult; Age Factors; Arthritis; Body Mass Index; Celiac disease; Celiac Disease - complications; Celiac Disease - diagnostic imaging; Cross-Sectional Studies; Enthesopathy - diagnostic imaging; Enthesopathy - etiology; Female; Humans; Inflammation; Inflammatory bowel diseases; Inflammatory Bowel Diseases - complications; Inflammatory Bowel Diseases - diagnostic imaging; Inflammatory diseases; Intestine; Male; Middle Aged; Permeability; Rheumatic diseases; Risk Factors; Severity of Illness Index; Spondyloarthropathy; Ultrasonography; Ultrasound
• ISSN: 1462-0324; 1462-0332
• DOI: 10.1093/rheumatology/key102

Abstract Objective Higher subclinical enthesitis on US has been reported in IBD and celiac disease, separately. The objective of this study was to compare IBD and celiac disease for enthesitis on US. Higher enthesitis scores in IBD compared with celiac disease would support a shared pathogenic mechanism between IBD and spondyloarthritis, whereas similar scores may suggest a general impact of gut inflammation on the enthesis. Methods Patients with IBD, celiac disease and healthy controls (HCs) were recruited and 12 entheses were scanned by US, blind to the diagnosis and clinical assessment. Elementary lesions for enthesitis were scored on a scale between 0 and 3, for inflammation, damage and total US scores. Results A total of 1260 entheses were scanned in 44 patients with celiac disease, 43 patients with IBD and 18 HCs. The three groups were matched for age and BMI. Patients with celiac disease and IBD had higher inflammation scores than HCs [10.4 (6.5), 9.6 (5.4) and 5.6 (5.2), respectively, P = 0.007) whereas damage scores were similar. Both age and BMI had significant effects on the entheseal scores, mostly for inflammation scores but when controlling for these the US enthesopathy scores were still higher in celiac disease and IBD. Conclusion The magnitude of subclinical enthesopathy scores is similar between celiac disease and IBD in comparison with HCs. These findings suggest that the common factor between both diseases and enthesopathy is abnormal gut permeability, which may be modified by the genetic architecture of IBD leading to clinical arthropathy.