首页> 外文期刊>Urology >Quercetin in men with category III chronic prostatitis: a preliminary prospective, double-blind, placebo-controlled trial.
【24h】

Quercetin in men with category III chronic prostatitis: a preliminary prospective, double-blind, placebo-controlled trial.

机译:患有III类慢性前列腺炎的男性中的槲皮素:一项初步的前瞻性,双盲,安慰剂对照试验。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVES: The National Institutes of Health (NIH) category III chronic prostatitis syndromes (nonbacterial chronic prostatitis and prostatodynia) are common disorders with few effective therapies. Bioflavonoids have recently been shown in an open-label study to improve the symptoms of these disorders in a significant proportion of men. The aim of this study was to confirm these findings in a prospective randomized, double-blind, placebo-controlled trial. METHODS: Thirty men with category IIIa and IIIb chronic pelvic pain syndrome were randomized in a double-blind fashion to receive either placebo or the bioflavonoid quercetin 500 mg twice daily for 1 month. The NIH chronic prostatitis symptom score was used to grade symptoms and the quality-of-life impact at the start and conclusion of the study. In a follow-up unblind, open-label study, 17 additional men received 1 month of a supplement containing quercetin, as well as bromelain and papain (Prosta-O), which enhance bioflavonoid absorption. RESULTS: Two patients in the placebo group refused to complete the study because of worsening symptoms, leaving 13 placebo and 15 bioflavonoid patients for evaluation in the blind study. Both the quercetin and placebo groups were similar in age, symptom duration, and initial symptom score. Patients taking placebo had a mean improvement in NIH symptom score from 20.2 to 18.8 (not significant), while those taking the bioflavonoid had a mean improvement from 21.0 to 13.1 (P = 0.003). Twenty percent of patients taking placebo and 67% of patients taking the bioflavonoid had an improvement of symptoms of at least 25%. In the 17 patients who received Prosta-Q in the open-label study, 82% had at least a 25% improvement in symptom score. CONCLUSIONS: Therapy with the bioflavonoid quercetin is well tolerated and provides significant symptomatic improvement in most men with chronic pelvic pain syndrome.
机译:目的:国立卫生研究院(NIH)的III类慢性前列腺炎综合征(非细菌性慢性前列腺炎和前列腺痛)是常见的疾病,几乎没有有效的治疗方法。最近,一项开放标签研究显示,生物类黄酮可在相当多的男性中改善这些疾病的症状。这项研究的目的是在一项前瞻性随机,双盲,安慰剂对照试验中证实这些发现。方法:以双盲方式将30名患有IIIa和IIIb类慢性盆腔疼痛综合征的男性随机分配,以接受安慰剂或生物类黄酮槲皮素500 mg的治疗,每天两次,共1个月。在研究开始和结束时,使用NIH慢性前列腺炎症状评分对症状和生活质量影响进行分级。在一项后续的无盲,开放标签研究中,另外有17名男性接受了1个月的补充品,其中含有槲皮素以及菠萝蛋白酶和木瓜蛋白酶(Prosta-O),它们可以增强生物类黄酮的吸收。结果:安慰剂组中有2名患者由于症状恶化而拒绝完成该研究,因此有13名安慰剂患者和15名生物类黄酮患者需要在盲法研究中进行评估。槲皮素和安慰剂组的年龄,症状持续时间和初始症状评分相似。服用安慰剂的患者NIH症状评分平均改善从20.2到18.8(不显着),而服用生物类黄酮的患者平均改善从21.0到13.1(P = 0.003)。服用安慰剂的患者占20%,服用生物类黄酮的患者占67%,症状改善至少25%。在开放标签研究中接受Prosta-Q的17例患者中,有82%的症状评分改善了至少25%。结论:生物类黄酮槲皮素的治疗耐受性良好,对大多数患有慢性盆腔疼痛综合症的男性可提供明显的症状改善。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号