阿托伐他汀联合curcetin对新冠肺炎(“长冠”)后不稳定型心绞痛患者炎症标志物的影响

R. Alieva, K. Fozilov, A. Shek, S. Khoshimov, M. M. Musabaev, L. Kan, A. Kim, Sh. A. Khodimetova
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摘要

目的:比较阿托伐他汀单药与阿托伐他汀联合姜黄素(姜黄素与槲皮素的混合物)对COVID-19(“长COVID”)后不稳定型心绞痛患者血脂和炎症生物标志物的影响。对186例不稳定型心绞痛患者进行了一项开放的简单比较随机研究,其中77例(I组)患者在纳入研究前4-8周内因COVID-19导致心绞痛不稳定,109例(II组)患者不稳定与感染无关。结果:ⅰ组hsc反应蛋白[5,4 (2,06-7,4)g/l]和il - 6,8,6 (5,4-10,3) pg/ml]水平分别高于ⅱ组[3,8 (1,2-4,0)g/l和6,9 (2,2-10,2)pg/ml] (P < 0.05)。在新冠肺炎患者的I亚组中,阿托伐他汀单药治疗(n = 43) 2个月后无显著疗效,而II亚组中阿托伐他汀联合curcetin治疗(n = 34) 2个月后hsCRP水平降低49.0% (P < 0.05), Il-6水平降低40.0% (P < 0.05)。在COVID-19后不稳定心绞痛患者中,与阿托伐他汀单药治疗相比,阿托伐他汀和curcetin联合治疗可降低炎症生物标志物的浓度。
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Effects of the combined use of atorvastatin and curcetin on inflammatory biomarkers in patients with unstable angina after COVID-19 (“Long COVID”)
Objective: To compare the effects of atorvastatin monotherapy and the combination of atorvastatin with curcetin (a mixture of the bioflavonoids curcumin and quercetin) on lipid profile and inflammatory biomarkers in patients with unstable angina after COVID-19 (“Long COVID”).Material. An open simple comparative randomized study was conducted in 186 patients with unstable angina, including 77 (Group I) in whom angina destabilization occurred as a result of COVID-19 during 4-8 weeks prior to inclusion in the study, and 109 patients (Group II) in whom destabilization was not associated with infection.Results: In group I, the level of hsC-reactive protein [5,4 (2,06-7,4) g/l and IL-6 8,6 (5,4-10,3) pg/ml] was higher (P < 0,05) than in group II patients [3,8 (1,2-4,0) g/l and 6,9 (2,2-10,2) pg/ml], respectively. In subgroup I of patients after COVID-19, atorvastatin monotherapy (n = 43) did not have a significant effect after two months of treatment, while in subgroup II the combined use of atorvastatin with curcetin (n = 34) for 2 months reduced the level of hsCRP by 49,0% (P < 0,05) and Il-6 by 40,0% (P < 0,05).Conclusion. In patients with unstable angina after COVID-19, combination treatment with atorvastatin and curcetin reduced concentrations of inflammatory biomarkers compared with atorvastatin monotherapy.
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