Mizuno Shinta, Ono Keiko, Mikami Yohei, Naganuma Makoto, Fukuda Tomohiro, Minami Kazuhiro, Masaoka Tatsuhiro, Terada Soichiro, Yoshida Takeshi, Saigusa Keiichiro, Hirahara Norimichi, Miyata Hiroaki, Suda Wataru, Hattori Masahira, Kanai Takanori
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Endoscopy Center, Edogawa Hospital, Tokyo, Japan.
Intest Res. 2020 Jan;18(1):69-78. doi: 10.5217/ir.2019.00084. Epub 2020 Jan 30.
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.
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.
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).
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.
背景/目的:5-氨基水杨酸(ASA)在一些患者中会引起不耐受反应。本研究旨在探讨溃疡性结肠炎(UC)合并5-ASA不耐受患者的预后,并评估5-ASA不耐受与肠道微生物群之间的潜在相互作用。
我们对就诊于参与研究医院的UC患者进行了一项回顾性队列研究。主要终点是比较5-ASA不耐受组和5-ASA耐受组在12个月内的住院发生率。次要终点是比较两组开始使用生物制剂后不良临床结局的风险。我们还在一个独立招募的UC患者队列中评估了5-ASA不耐受与微生物变化之间的相关性。
793例患者中,59例(7.4%)被分配到5-ASA不耐受组,734例(92.5%)被分配到5-ASA耐受组。不耐受组的入院率和使用皮质类固醇的发生率显著高于耐受组(P<0.001)。在108例接受抗肿瘤坏死因子生物制剂治疗的患者中,5-ASA不耐受增加了开始使用生物制剂后额外诱导治疗的发生率(P<0.001)。5-ASA不耐受组粪便杆菌属、链球菌属和梭菌属中的细菌丰度高于5-ASA耐受组(P<0.05)。
在UC患者中,5-ASA不耐受与不良临床结局风险和生态失调相关。对5-ASA给药进行细菌治疗优化可能对改善UC患者的预后很重要。