A Pilot Study to Evaluate the Safety and Efficacy of an Oral Dose of (-)-Epigallocatechin-3-Gallate-Rich Polyphenon E in Patients With Mild to Moderate Ulcerative Colitis

被引:106
作者
Dryden, Gerald W. [1 ]
Lam, Allan [1 ]
Beatty, Karen [2 ]
Qazzaz, Hassan H. [1 ]
McClain, Craig J. [1 ]
机构
[1] Univ Louisville, Div Gastroenterol Hepatol & Nutr, Louisville, KY 40292 USA
[2] Univ Louisville, Clin Res Ctr, Louisville, KY 40292 USA
基金
美国国家卫生研究院;
关键词
ulcerative colitis; green tea polyphenols; (-)-epigallocatechin-3-gallate; EGCG; complementary and alternative medicine; CAM; INFLAMMATORY-BOWEL-DISEASE; NECROSIS-FACTOR-ALPHA; FACTOR-KAPPA-B; GREEN TEA; EPIGALLOCATECHIN-GALLATE; SIGNALING PATHWAYS; MEDICINE USE; CANCER; CELLS; ACTIVATION;
D O I
10.1097/MIB.0b013e31828f5198
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background:Green tea and its main polyphenolic component, (-)-epigallocatechin-3-gallate (EGCG), exert powerful anti-inflammatory effects that are protective against both inflammatory diseases and cancer. Research with animal and human cell lines provide plausible support for these claims. Poor absorption results in low systemic bioavailability of EGCG after oral administration but high colonic mucosal exposure.Methods:Patients with mild to moderate ulcerative colitis (UC) were randomized to daily doses of oral Polyphenon E (400 mg or 800 mg of total EGCG daily, administered in split doses) or placebo in a double-blinded, placebo-controlled pilot study. Response was measured by the UC disease activity index and the inflammatory bowel disease questionnaire on day 56.Results:Twenty patients were randomized to active therapy or placebo in a 4:1 ratio. Nineteen subjects received >1 dose of study medication (15 Polyphenon E, 4 placebo). The mean UC disease activity index score at study entry was 6.5 1.9 in the treatment group and 7.3 +/- 1.7 in the placebo group. After 56 days of therapy, the response rate was 66.7% (10 of 15) in the Polyphenon E group and 0% (0 of 4) in the placebo group (P = 0.03). The active treatment remission rate was 53.3% (8 of 15) compared with 0% (0 of 4) for placebo (P = 0.10). Polyphenon E treatment resulted in only minor side effects.Conclusions:Administration of Polyphenon E resulted in a therapeutic benefit for patients who were refractory to 5-aminosalicylic and/or azathioprine. This agent holds promise as a novel option for the treatment of patients with UC with mild to moderately active disease.
引用
收藏
页码:1904 / 1912
页数:9
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