Curcumin in Combination With Mesalamine Induces Remission in Patients With Mild-to-Moderate Ulcerative Colitis in a Randomized Controlled Trial

被引:264
作者
Lang, Alon [1 ]
Salomon, Nir [1 ,2 ,3 ]
Wu, Justin C. Y. [4 ,5 ]
Kopylov, Uri [1 ]
Lahat, Adi [1 ]
Har-Noy, Ofir [1 ]
Ching, Jessica Y. L. [4 ,5 ]
Cheong, Pui Kuan [4 ,5 ]
Avidan, Benjamin [1 ]
Gamus, Dorit [2 ,3 ]
Kaimakliotis, Ioannis [6 ]
Eliakim, Rami [1 ]
Ng, Siew C. [4 ,5 ]
Ben-Horin, Shomron [1 ]
机构
[1] Tel Aviv Univ, Dept Gastroenterol, Tel Hashomer, Israel
[2] Tel Aviv Univ, Complementary Med Serv, Sheba Med Ctr, Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Sch Med, Tel Hashomer, Israel
[4] Chinese Univ Hong Kong, Inst Digest Dis, Hong Kong, Hong Kong, Peoples R China
[5] Chinese Univ Hong Kong, Hong Kong Inst Integrat Med, Hong Kong, Hong Kong, Peoples R China
[6] Cent IBD Clin, Nicosia, Cyprus
关键词
IBD; Clinical Trial; Inflammatory Bowel Disease; Phytochemical; NF-KAPPA-B; DOUBLE-BLIND; END-POINTS; PLACEBO; THERAPY; DISEASE; NCB-02; ENEMA; MICE;
D O I
10.1016/j.cgh.2015.02.019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: The phytochemical compound curcumin was reported to be effective in maintaining remission in patients with ulcerative colitis (UC). We investigated curcumin's efficacy in inducing remission in patients with active mild-to-moderate UC. METHODS: We performed a multicenter randomized, placebo-controlled, double-blind study of 50 mesalamine-treated patients with active mild-to-moderate UC (defined by the Simple Clinical Colitis Activity Index [SCCAI]) who did not respond to an additional 2 weeks of the maximum dose of mesalamine oral and topical therapy. Patients were randomly assigned to groups who were given curcumin capsules (3 g/day, n = 26) or an identical placebo (n = 24) for 1 month, with continued mesalamine. The primary outcome was the rate of clinical remission (SCCAI <= 2) at week 4. Clinical and endoscopic responses were also recorded. RESULTS: In the intention-to-treat analysis, 14 patients (53.8%) receiving curcumin achieved clinical remission at week 4, compared with none of the patients receiving placebo (P = .01; odds ratio [OR], 42; 95% confidence interval [CI], 2.3-760). Clinical response (reduction of >= 3 points in SCCAI) was achieved by 17 patients (65.3%) in the curcumin group vs 3 patients (12.5%) in the placebo group (P < .001; OR, 13.2; 95% CI, 3.1-56.6). Endoscopic remission (partial Mayo score <= 1) was observed in 8 of the 22 patients evaluated in the curcumin group (38%), compared with none of 16 patients evaluated in the placebo group (P = .043; OR, 20.7; 95% CI, 1.1-393). Adverse events were rare and comparable between the 2 groups. CONCLUSIONS: Addition of curcumin to mesalamine therapy was superior to the combination of placebo and mesalamine in inducing clinical and endoscopic remission in patients with mild-to-moderate active UC, producing no apparent adverse effects. Curcumin may be a safe and promising agent for treatment of UC. Clinicaltrials.gov number: NCT01320436.
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页码:1444 / +
页数:7
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