Efficacy and safety of curcumin in patients with metabolic phenotype of osteoarthritis: A pilot study

I. Shirinsky, V. Shirinsky, K. Filatova
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Abstract

The aim of this study was to assess efficacy and safety of curcumin in metabolic syndrome- associated osteoarthritis (MetS-OA). All patients provided written informed consent. Knee OA was diagnosed according to American College of Rheumatology criteria; MetS was diagnosed according to Russian Scientific Society of Cardiology Guidelines. The study had before-and-after design. The main inclusion criteria were presence of knee OA and MetS, levels of global health assessment and pain assessment more than 50 mm using 0-100 visual analogue scale (VAS). The main outcome was VAS global. The other outcomes were VAS pain, Knee injury and Osteoarthritis Outcome Score (KOOS) consisting of five subscales: pain (KOOS pain), other symptoms (KOOS symptoms), activities in daily living (KOOS ADL), function in sport and recreation (KOOS Sport/Rec) and knee related Quality of life (KOOS QoL). The level of depression was measured using PHQ- 9. For pain, proportion of patients achieving minimal clinically important improvement (MCII) was assessed using the cut-offs of (a) 15 of 100 for absolute improvement and 20% for relative improvement.The treatment consisted of C. longa extract 1000 mg/day for 4 weeks. The assessments were performed on baseline and 4 weeks thereafter. Eighteen women with MetS-OA of the knee were included in the study.At the end of treatment, there were significant improvements in the VAS global scale by an average 33.9 mm (p = 0.001), VAS pain by 25 mm (p = 0.001). There was a trend towards improvement in PHQ-9 by 2.9 (p = 0.05). The mean improvement in KOOS pain was 11 (p = 0.001). KOOS symptoms improved by 9 (p = 0.025), KOOS ADL - by 12.4 (p = 0.001), KOOS Sport/Rec by 10.3 (p = 0.044), and KOOS QOL by 14.4 (p = 0.009). The proportion of patients achieving clinically significant improvement (MCII) were nine (56%) for both global health and pain. There were no adverse events during the study. The findings of this study suggest clinical efficacy and safety of C. Longa in MetS-associated knee OA. There is a need for large controlled studies to confirm these results.
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姜黄素在代谢性骨关节炎患者中的疗效和安全性:一项初步研究
本研究的目的是评估姜黄素治疗代谢综合征相关性骨关节炎(MetS-OA)的疗效和安全性。所有患者均提供书面知情同意书。膝关节OA诊断依据美国风湿病学会标准;MetS是根据俄罗斯科学学会心脏病学指南诊断的。该研究采用了前后对比设计。主要纳入标准是膝关节OA和MetS的存在,整体健康评估水平和疼痛评估超过50 mm(使用0-100视觉模拟量表(VAS))。主要结果是VAS全球评分。其他结果包括VAS疼痛、膝关节损伤和骨关节炎结局评分(oos),该评分由五个亚量表组成:疼痛(oos疼痛)、其他症状(oos症状)、日常生活活动(oos ADL)、运动和娱乐功能(oos sport /Rec)和膝关节相关生活质量(oos QoL)。采用PHQ- 9测定抑郁水平。对于疼痛,达到最小临床重要改善(MCII)的患者比例使用绝对改善(a)的截断值为15 / 100,相对改善为20%。治疗方法为龙骨提取物1000 mg/d,连续4周。评估分别在基线和4周后进行。18名患有膝关节炎的女性被纳入研究。治疗结束时,VAS总体评分平均改善33.9 mm (p = 0.001), VAS疼痛平均改善25 mm (p = 0.001)。PHQ-9有提高2.9分的趋势(p = 0.05)。kos疼痛的平均改善为11 (p = 0.001)。KOOS症状改善9例(p = 0.025), KOOS ADL -改善12.4例(p = 0.001), KOOS Sport/Rec改善10.3例(p = 0.044), KOOS QOL改善14.4例(p = 0.009)。在总体健康和疼痛方面实现临床显著改善(MCII)的患者比例为9(56%)。研究期间无不良事件发生。本研究结果提示C. Longa治疗mets相关性膝关节炎的临床疗效和安全性。有必要进行大规模的对照研究来证实这些结果。
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来源期刊
Medical Immunology (Russia)
Medical Immunology (Russia) Medicine-Immunology and Allergy
CiteScore
0.70
自引率
0.00%
发文量
88
审稿时长
12 weeks
期刊介绍: The journal mission is to promote scientific achievements in fundamental and applied immunology to various medical fields, the publication of reviews, lectures, essays by leading domestic and foreign experts in the field of fundamental and experimental immunology, clinical immunology, allergology, immunodiagnostics and immunotherapy of infectious, allergy, autoimmune diseases and cancer.
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