低剂量口服姜黄素对轻度至中度溃疡性结肠炎的缓解诱导无效:来自随机双盲安慰剂对照试验的结果。

Saurabh Kedia, Vikram Bhatia, Sandeep Thareja, Sushil Garg, Venigalla Pratap Mouli, Sawan Bopanna, Veena Tiwari, Govind Makharia, Vineet Ahuja
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引用次数: 56

摘要

目的:评价口服姜黄素对轻中度溃疡性结肠炎(UC)患者临床缓解的作用。方法:2003年1月至2005年3月,采用前瞻性随机双盲安慰剂对照试验,比较口服姜黄素和2.4 g美沙拉胺与安慰剂和2.4 g美沙拉胺对轻至中度溃疡性结肠炎患者的缓解效果。纳入的患者接受1胶囊安慰剂或姜黄素(150毫克),每天三次,持续8周。在第0、4和8周对患者进行临床和内窥镜检查。8周时的主要终点是临床缓解,8周时的次要终点是临床反应、粘膜愈合和治疗失败。主要分析是治疗最坏情况(ITT-WCS)的意向。结果:在300例UC患者中,62例患者(姜黄素:29例,安慰剂:33例)符合纳入标准,并在基线时随机分组。其中,21名患者没有完成试验,41名患者(姜黄素:16名,安慰剂:25名)最终完成8周。8周时,姜黄素组和安慰剂组的临床缓解率(31.3% vs 27.3%, P = 0.75)、临床缓解率(20.7% vs 36.4%, P = 0.18)、粘膜愈合率(34.5% vs 30.3%, P = 0.72)和治疗失败率(25% vs 18.5%, P = 0.59)均无显著差异。结论:低剂量口服姜黄素450mg /d对轻、中度UC患者的缓解无效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Low dose oral curcumin is not effective in induction of remission in mild to moderate ulcerative colitis: Results from a randomized double blind placebo controlled trial.

Aim: To evaluate the role of oral curcumin in inducing clinical remission in patients with mild to moderate ulcerative colitis (UC).

Methods: A prospective randomized double-blind placebo-controlled trial comparing the remission inducing effect of oral curcumin and mesalamine 2.4 g with placebo and mesalamine 2.4 g in patients of ulcerative colitis with mild to moderate severity was conducted from January 2003 to March 2005. The included patients received 1 capsule thrice a day of placebo or curcumin (150 mg) for 8 wk. Patients were evaluated clinically and endoscopically at 0, 4 and 8 wk. The primary outcome was clinical remission at 8 wk and secondary outcomes were clinical response, mucosal healing and treatment failure at 8 wk. The primary analysis was intention to treat worst case scenario (ITT-WCS).

Results: Of 300 patients with UC, 62 patients (curcumin: 29, placebo: 33) fulfilled the inclusion criteria and were randomized at baseline. Of these, 21 patients did not complete the trial, 41 patients (curcumin: 16, placebo: 25) finally completed 8 wk. There was no significant difference in rates of clinical remission (31.3% vs 27.3%, P = 0.75), clinical response (20.7% vs 36.4%, P = 0.18), mucosal healing (34.5% vs 30.3%, P = 0.72), and treatment failure (25% vs 18.5%, P = 0.59) between curcumin and placebo at 8 wk.

Conclusion: Low dose oral curcumin at a dose of 450 mg/d was ineffective in inducing remission in mild to moderate cases of UC.

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