Importance of rectal over colon status in ulcerative colitis remission: the role of microinflammation and mucosal barrier dysfunction in relapse

被引:0
作者
Nishioka, Kei [1 ,2 ]
Ogino, Haruei [2 ,3 ]
Ihara, Eikichi [2 ]
Chinen, Takatoshi [2 ]
Kimura, Yusuke [2 ]
Esaki, Mitsuru [2 ,4 ]
Bai, Xiaopeng [2 ]
Minoda, Yosuke [2 ]
Tanaka, Yoshimasa [2 ]
Wada, Masafumi [2 ]
Hata, Yoshitaka [2 ]
Ambrosini, Yoko M. [5 ]
Ogawa, Yoshihiro [2 ]
机构
[1] Saiseikai Futsukaichi Hosp, Dept Gastroenterol, Chikushino, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Med & Bioregulatory Sci, Fukuoka, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Dept Gastroenterol & Metab, Fukuoka, Japan
[4] Mayo Clin, Div Gastroenterol & Hepatol, Scottsdale, AZ USA
[5] Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA USA
关键词
Ulcerative colitis; Remission; Relapse; Microinflammation; Impaired mucosal barrier function; INFLAMMATORY-BOWEL-DISEASE; TIGHT JUNCTIONS; PERMEABILITY; EXPRESSION;
D O I
10.1007/s00535-024-02199-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundUlcerative colitis (UC) is a refractory inflammatory disease that affects the rectum and colon, with pivotal involvement of the rectal environment in relapse initiation. This study was conducted in two phases to examine the differences in gene expression between the rectum and colon and to identify relapse factors.MethodsIn ***Study 1, RNA sequencing was performed on biopsies from the colon and rectum of patients with active UC, those with remission UC, and controls. In Study 2, the mucosal impedance (MI) values reflecting mucosal barrier function and the mRNA expression of tight junction proteins and inflammatory cytokines were examined in 32 patients with remission UC and 22 controls. Relapse was monitored prospectively.ResultsIn Study 1, comprehensive genetic analysis using RNA sequencing revealed distinct gene profiles in the rectum and sigmoid colon of patients with remission UC. The rectum of these patients exhibited an enriched immune response and apical junction phenotype with persistent upregulation of CLDN2 gene expression. In Study 2, even in patients with remission UC, the MI values in the rectum, but not in the sigmoid colon, were significantly decreased, whereas they were negatively correlated with CLDN2, IL-1 beta, and IL-6 expressions.ConclusionThe status of the rectum in patients with remission UC differs from that of the colon, with microinflammation and impaired mucosal barrier function, which are associated with the upregulation of CLDN2, playing a role in relapse.
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页码:416 / 429
页数:14
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