Departments of Gastroenterology.
Microbiology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
J Clin Gastroenterol. 2022 Sep 1;56(8):705-711. doi: 10.1097/MCG.0000000000001609. Epub 2021 Sep 9.
There is an emerging role of fungal dysbiosis in the pathogenesis of inflammatory bowel disease. Prevalence of Candida in patients with active ulcerative colitis (UC) and the effect of fluconazole therapy in reducing disease activity of UC are not known.
All consecutive consenting patients with active UC defined as Mayo score ≥3 were evaluated for presence of Candida by stool culture and predictors for presence of Candida were identified. Those who had evidence of Candida in the stool were randomized to receive oral fluconazole 200 mg daily or placebo for 3 weeks along with standard medical therapy. Patients were assessed by clinical, sigmoidoscopy, and laboratory parameters at baseline and at 4 weeks. The primary outcome was clinical and endoscopic response at 4 weeks defined by a 3-point reduction in Mayo score. Secondary outcomes were reduction in fecal calprotectin, histologic response, and adverse events.
Of the 242 patients with active UC, 68 (28%) patients had Candida in stool culture. Independent predictors for presence of Candida in patients with active UC were partial Mayo score of ≥3 and steroid exposure. Among those with Candida on stool culture (n=68), 61 patients fulfilled eligibility criteria and were randomized to receive fluconazole (n=31) or placebo (n=30). Three-point reduction in Mayo score though was numerically higher in the fluconazole group than the placebo group but was not statistically significant [5 (16.1%) vs. 1 (3.33%); P =0.19]. Postintervention median Mayo score was lower in fluconazole than placebo group [4 (3, 5) vs. 5 (4, 6); P =0.034]. Patients in fluconazole group had more often reduction in fecal calprotectin [26 (83.9%) vs. 11 (36.7%); P =0.001] and histologic scores [23 (74.1%) vs. 10 (33.3%); P =0.001] compared with placebo. All patients were compliant and did not report any serious adverse event.
Candida colonization is found in 28% of patients with UC. Steroid exposure and active disease were independent predictors for the presence of Candida . There was no statistically significant difference in the number of patients who achieved 3-point reduction in Mayo score between 2 groups. However, clinical, histologic, and calprotectin levels showed significant improvement in fluconazole group.
真菌失调在炎症性肠病的发病机制中起着重要作用。目前尚不清楚活动期溃疡性结肠炎(UC)患者中念珠菌的患病率,以及氟康唑治疗对降低 UC 疾病活动度的效果。
所有符合条件的活动期 UC 患者(Mayo 评分≥3 分)均通过粪便培养评估念珠菌的存在情况,并确定念珠菌存在的预测因素。对粪便中存在念珠菌的患者随机分为氟康唑 200mg 每日 1 次口服或安慰剂治疗 3 周,同时给予标准的医学治疗。患者在基线和 4 周时通过临床、乙状结肠镜和实验室参数进行评估。主要终点为 4 周时的临床和内镜应答,定义为 Mayo 评分降低 3 分。次要终点为粪便钙卫蛋白减少、组织学应答和不良事件。
在 242 例活动期 UC 患者中,68 例(28%)患者粪便培养出念珠菌。活动期 UC 患者中念珠菌存在的独立预测因素为部分 Mayo 评分≥3 分和激素暴露。在粪便培养出念珠菌的 68 例患者中(n=68),61 例符合入组标准并随机分为氟康唑(n=31)或安慰剂(n=30)组。氟康唑组较安慰剂组 Mayo 评分降低 3 分的患者比例虽有升高但无统计学意义[5(16.1%)vs. 1(3.33%);P=0.19]。氟康唑组较安慰剂组治疗后中位数 Mayo 评分更低[4(3,5)vs. 5(4,6);P=0.034]。氟康唑组患者粪便钙卫蛋白降低更常见[26(83.9%)vs. 11(36.7%);P=0.001],组织学评分降低更常见[23(74.1%)vs. 10(33.3%);P=0.001]。所有患者均能耐受药物,且未报告任何严重不良事件。
UC 患者中有 28%存在念珠菌定植。激素暴露和疾病活动是念珠菌存在的独立预测因素。两组间 Mayo 评分降低 3 分的患者数量无统计学差异。然而,氟康唑组患者的临床、组织学和钙卫蛋白水平有显著改善。