5-Aminosalicylic acid intolerance is associated with a risk of adverse clinical outcomes and dysbiosis in patients with ulcerative colitis

被引:23
作者
Mizuno, Shinta [1 ]
Ono, Keiko [1 ]
Mikami, Yohei [1 ]
Naganuma, Makoto [1 ]
Fukuda, Tomohiro [1 ]
Minami, Kazuhiro [1 ]
Masaoka, Tatsuhiro [1 ]
Terada, Soichiro [2 ]
Yoshida, Takeshi [3 ]
Saigusa, Keiichiro [4 ]
Hirahara, Norimichi [5 ]
Miyata, Hiroaki [5 ]
Suda, Wataru [6 ]
Hattori, Masahira [6 ]
Kanai, Takanori [1 ]
机构
[1] Keio Univ, Div Gastroenterol & Hepatol, Dept Internal Med, Sch Med, Tokyo, Japan
[2] Edogawa Hosp, Endoscopy Ctr, Tokyo, Japan
[3] Saitama Med Ctr, Dept Gastroenterol & Hepatol, Saitama, Japan
[4] Tokyo Saiseikai Cent Hosp, Dept Gastroenterol & Hepatol, Tokyo, Japan
[5] Keio Univ, Dept Hlth Policy & Management, Sch Med, Tokyo, Japan
[6] RIKEN, Ctr Integrat Med Sci, Lab Microbiome Sci, Yokohama, Kanagawa, Japan
关键词
5-Aminosalicylic acid; Colitis; ulcerative; Prognosis; Dysbiosis; FECAL MICROBIOTA TRANSPLANTATION; INFLAMMATORY-BOWEL-DISEASE; GUT MICROBIOME; METAANALYSIS; DESENSITIZATION; SULFASALAZINE; OBESITY; MESALAZINE; REMISSION; EFFICACY;
D O I
10.5217/ir.2019.00084
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: 5-Aminosalicylic acid (ASA) causes intolerance reactions in some patients. This study was performed to examine the prognosis of patients with ulcerative colitis (UC) and 5-ASA intolerance, and to evaluate the potential interaction between 5-ASA intolerance and the intestinal microbiota. Methods: We performed a retrospective cohort study of patients with UC who visited participating hospitals. The primary endpoint was to compare the incidence of hospitalization within 12 months between the 5-ASA intolerance group and the 5-ASA tolerance group. The secondary endpoint was to compare the risk of adverse clinical outcomes after the start of biologics between the 2 groups. We also assessed the correlation between 5-ASA intolerance and microbial change in an independently recruited cohort of patients with UC. Results: Of 793 patients, 59 (7.4%) were assigned to the 5-ASA intolerance group and 734 (92.5%) were assigned to the 5-ASA tolerance group. The admission rate and incidence of corticosteroid use were significantly higher in the intolerance than tolerance group (P < 0.001). In 108 patients undergoing treatment with anti-tumor necrosis factor biologics, 5-ASA intolerance increased the incidence of additional induction therapy after starting biologics (P < 0.001). The 5-ASA intolerance group had a greater abundance of bacteria in the genera Faecalibacterium, Streptococcus, and Clostridium than the 5-ASA tolerance group (P < 0.05). Conclusions: In patients with UC, 5-ASA intolerance is associated with a risk of adverse clinical outcomes and dysbiosis. Bacterial therapeutic optimization of 5-ASA administration may be important for improving the prognosis of patients with UC.
引用
收藏
页码:69 / +
页数:13
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