KMID : 0988920220200040475
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Intestinal Research 2022 Volume.20 No. 4 p.475 ~ p.481
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Clinical features of very early-onset inflammatory bowel disease in Japan: a retrospective single-center study
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Usami Masaaki
Takeuchi Ichiro Kyodo Reiko Hirano Yuri Kashiwagi Kosuke Fujikawa Hiroki Shimizu Hirotaka Kawa Toshinao Arai Katsuhiro
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Abstract
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Background/Aims: Very early-onset inflammatory bowel disease (VEO-IBD), defined as IBD diagnosed in patients younger than 6 years, is a challenge for pediatric gastroenterologists. Although there have been reports regarding VEO-IBD in Western countries, those in Asia are still lacking. This study aimed to investigate the clinical features of Japanese VEO-IBD patients.
Methods: Patients with VEO-IBD diagnosed between 2006 and 2019 were evaluated retrospectively. The disease phenotypes were classified into ulcerative colitis type (UC-type) and Crohn¡¯s disease type (CD-type), and the clinical features and courses were compared between the phenotypes.
Results: Overall, 54 VEO-IBD patients (19 patients with UC-type and 35 patients with CD-type) were evaluated. The median age at onset was 18 months. One patient had severe combined immunodeficiency (SCID), and 9 patients had monogenic IBD. Monogenic IBD was more prevalent in the CD-type patients with perianal disease (CD-type (PD)). The age at onset was significantly lower in the CD-type group (P<0.05). The most common initial symptom was bloody stools (70%), followed by diarrhea (63%), weight loss (24%), fever (20%), and perianal disease (20%). Excluding patients with SCID and monogenic IBD, 23 out of 44 patients (52%) required biologics. The biologics were switched in 11 out of 44 patients (25%), and the majority of these patients (82%) were in the CD-type group. Overall, 9 patients (20%) required intestinal resection or ostomy placement.
Conclusions: CD-type tends to occur at an earlier age, and monogenic IBD occurs significantly more frequently in CD-type (PD). Disease severity and treatment should be individualized, owing to the disease heterogeneity.
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KEYWORD
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Monogenic inflammatory bowel disease, Japan, Phenotype, Disease severity, Therapeutics
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