Department of Cardiology, The Key Lab of Cardiovascular Disease of Wenzhou, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province 325035, China.
Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province 310000, China.
Oxid Med Cell Longev. 2020 Jan 9;2020:1520747. doi: 10.1155/2020/1520747. eCollection 2020.
Since the first report in 2005, accumulating interests have been focused on the effect of curcumin in atherosclerosis with discrepancies. Therefore, we conducted a systematic review and meta-analysis to comprehensively estimate its effect against atherosclerosis. Literature search was performed on the database of PubMed, EMBASE, and Cochrane Library to identify relevant studies which estimated the effect of curcumin in atherosclerosis. Reporting effects on aortic lesion area was the primary outcome while effects on serum lipid profiles and circulating inflammatory markers were the secondary outcome. A total of 10 studies including 14 independent pairwise experiments were included in our analysis. We clarified that curcumin could significantly reduce aortic atherosclerotic lesion area (SMD = -0.89, 95% CI: -1.36 to -0.41, = 0.0003), decrease serum lipid profiles (Tc, MD = -1.005, 95% CI: -1.885 to -0.124, = 0.025; TG, MD = -0.045, 95% CI: -0.088 to -0.002, = 0.042; LDL-c, MD = -0.523, 95% CI: -0.896 to -0.149, = 0.006) as well as plasma inflammatory indicators (TNF-, MD = -56.641, 95% CI: -86.848 to -26.433, < 0.001; IL-1, MD = -5.089, 95% CI: -8.559 to -1.619, = 0.004). Dose-response meta-analysis predicted effective dosage of curcumin between 0 and 347 mg/kg BW per day, which was safe and nontoxic according to the existing publications. The underlying mechanisms were also discussed and might be associated with the modulation of lipid transport and inflammation in cells within artery walls as well as indirect modulations in other tissues. Clinical evidence from nonatherosclerosis populations revealed that curcumin would lower the lipid profiles and inflammatory responses as it has in a mouse model. However, standard preclinical animal trial designs are still needed; further studies focusing on the optimal dose of curcumin against atherosclerosis and RCTs directly in atherosclerosis patients are also warranted.
自 2005 年首次报道以来,人们对姜黄素在动脉粥样硬化中的作用产生了越来越多的兴趣,但研究结果存在差异。因此,我们进行了系统评价和荟萃分析,以全面评估其对动脉粥样硬化的作用。我们在 PubMed、EMBASE 和 Cochrane Library 数据库中进行了文献检索,以确定评估姜黄素对动脉粥样硬化作用的相关研究。报告主动脉病变面积的影响是主要结局,而报告血清脂质谱和循环炎症标志物的影响是次要结局。我们的分析共纳入了 10 项研究,包括 14 项独立的两两实验。我们明确指出,姜黄素可以显著降低主动脉粥样硬化病变面积(SMD=-0.89,95%CI:-1.36 至-0.41, = 0.0003),降低血清脂质谱(TC,MD=-1.005,95%CI:-1.885 至-0.124, = 0.025;TG,MD=-0.045,95%CI:-0.088 至-0.002, = 0.042;LDL-c,MD=-0.523,95%CI:-0.896 至-0.149, = 0.006)以及血浆炎症指标(TNF-,MD=-56.641,95%CI:-86.848 至-26.433, <0.001;IL-1,MD=-5.089,95%CI:-8.559 至-1.619, = 0.004)。剂量反应荟萃分析预测姜黄素的有效剂量在 0 至 347mg/kgBW/天之间,根据现有文献,该剂量是安全且无毒的。我们还讨论了其潜在机制,其可能与调节动脉壁细胞内的脂质转运和炎症以及对其他组织的间接调节有关。来自非动脉粥样硬化人群的临床证据表明,姜黄素可以降低血脂谱和炎症反应,就像在小鼠模型中一样。然而,仍需要标准的临床前动物试验设计;还需要进一步研究姜黄素对动脉粥样硬化的最佳剂量以及直接在动脉粥样硬化患者中进行的 RCT。