姜黄素改善第4步哮喘治疗:安慰剂对照,单盲研究

E. Jusufovic, M. Košnik, N. Arifhodzic, J. Nurkić, M. Al‐Ahmad, Azra Jusufovic, Dženan Halilović, R. Sejdinović
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引用次数: 3

摘要

背景:尽管采取了多步骤的努力,许多哮喘患者仍然有症状。显示姜黄素的抗炎活性。本研究的目的是分析姜黄素辅助治疗对哮喘患者炎症参数、肺功能、疾病控制和生活质量的影响。研究对象和方法:对150例不吸烟的哮喘患者进行了为期3个月的研究,这些患者接受稳定、中等剂量的吸入糖皮质激素(IGK)治疗,分为三组(n=50):姜黄素组(每天两次接受姜黄素500毫克)、安慰剂组(接受安慰剂片)和对照组(不干预)。比较研究前后及组间痰嗜酸性粒细胞(sEo)、血嗜酸性粒细胞(bEo)、高敏c反应蛋白(hsCRP)、预测第一秒用力呼气量(FEV1%)、哮喘控制试验(ACT)、哮喘生活质量问卷(mAQLQ)。结果:研究前,各组间随访参数基本一致。研究结束后,各组FEV1%、ACT和AQLQ均有改善,但姜黄素组改善效果较安慰剂组和对照组更为显著。姜黄素组仅改善了sEo、bEo和hsCRP。此外,与安慰剂和对照组相比,姜黄素组在ACT评分(变化bb0.3)和mAQLQ评分(变化≥0.5)方面表现出更频繁的临床显著改善。另一方面,研究结束后,FEV1%、ACT、maqql、hsCRP、sEo、bEo在安慰剂组和对照组的分布相似。结论:这是第一个安慰剂对照和单盲研究,表明姜黄素附加治疗可以改善中度部分控制哮喘患者的肺功能、疾病控制和生活质量。未来的研究可能受益于更大的样本量、更长的研究时间、双盲设计、不同剂量的姜黄素和/或口服生物利用度的改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Curcumin improves step 4 asthma treatment: placebo-controlled, single blind study
Background: Despite multistep efforts, many asthma patients remain symptomatic. Anti-inflammatory activities of curcumin are shown. Aim of the study was to analyse the impact of curcumin add-on therapy on inflammatory parameters, lung function, disease control and quality of life in asthma patients. Subjects and methods: Three-months lasting study was done on 150 non-smokers with asthma, that were treated with stable, moderate dose of inhaled glucocorticoids (IGK) and divided into three groups (n=50 each): curcumin group (receiving curcumin 500 mg per os twice daily), placebo group (receiving placebo tablets) and control (non-intervention) group. Sputum eosinophils (sEo), blood eosinophils (bEo), high sensitive C-reactive protein (hsCRP), predicted forced expiratory volume in first second (FEV1%), Asthma Control Test (ACT) and mini Asthma Quality of Life Questionnaire (mAQLQ) were compared before and after study, as well as between groups. Results: Before study, all followed parameters were similar between groups. After study, FEV1%, ACT and AQLQ were improved in all groups, but these improvements were more prominent in curcumin group than in placebo and control. Additionally curcumin group only showed improvement in sEo, bEo and hsCRP. Furthermore, curcumin group showed more frequent clinically significant improvement in ACT score (change>3) and in mAQLQ score (change≥0.5) when compared to placebo and control. On the other side, after study FEV1%, ACT, mAQLQ, hsCRP, sEo and bEo were similarly distributed among placebo and control group. Conclusion: This is the first placebo controlled and single-blind study to suggest that add-on therapy with curcumin could improve lung function, disease control and quality of life in moderate partially controlled asthma. Future studies may benefit from a larger sample size, longer study duration, double blind design, different dose of curcumin and/or improvements in oral bioavailability.
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