新冠肺炎后代谢综合征患者IL-6家族细胞因子、脂联素和瘦素水平的变化

O. Radaeva, A. Simbirtsev, Y. Kostina, E. Negodnova, D. D. Besheynov, S. V. Mashnina, V. Eremeev
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引用次数: 0

摘要

COVID-19是一种多系统疾病,但目前对其后果的程度知之甚少,特别是对代谢紊乱患者。本研究旨在评价代谢综合征(MetS)患者感染SARS-CoV-2后360天内IL-6家族细胞因子(IL-6和sIL-6、LIF和sLIFr)、脂联素和瘦素的特殊变化,以了解与既往接种COVID-19相关的免疫发病特征。我们将患者分为两组:(1)在全程接种载体疫苗后6-12个月感染COVID-19的MetS患者(n = 32);(2)接受COVID-19治疗但未接种疫苗的MetS患者(n = 29)。对照组包括没有MetS的条件健康个体:(3)接种疫苗,(4)未接种疫苗,同时患有COVID-19。ELISA法检测各组血清IL-6、sIL-6、LIF、sLIFr、瘦素、脂联素、NO、ADMA、SDMA水平。在MetS患者中,细胞因子对促炎反应的调节发生了变化(血液IL-6和瘦素水平升高),这在MetS患者中在covid后的前30天内最为明显,但在12个月内仍有一些变化(例如血液中瘦素浓度升高)。针对COVID-19的疫苗接种降低了sIL- 6r/ IL-6和瘦素/脂联素系统对保护性脂联素的促炎变化的严重程度。然而,瘦素的持续增加并没有被取消。在解释这些结果时,在接种过MetS的人群中,关于上述细胞因子在COVID-19后1年内对MetS的调节,没有发现负性差异。血清sIL-6r/IL-6、LIF/ sLIFr、脂联素和瘦素含量与血管活性物质(NO、ADMA和SDMA)、糖化血红蛋白、LDL水平的单因素及多因素相关分析表明,sIL-6r/IL-6比值升高是NO降低的独立因素(r = 0.74, p 0.01);sLIFr的增加与糖化血红蛋白的增加呈正相关(r = 0.69, p 0.01),与ADMA的增加相关(r = 0.82, p 0.001),瘦素(在该模型中)被证明是LDL增加的独立因素(r = 0.69, p 0.05)。COVID-19前可改变因素的影响,特别是疫苗接种,在降低COVID-19后MetS患者原有慢性疾病(高血压、动脉粥样硬化、糖尿病)进展的可能性方面具有相关性,并且具有应用于临床实践的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytokines of the IL-6 family, adiponectin and leptin levels in patients with metabolic syndrome during the post-COVID period
COVID-19 is a multisystem disease, but the extent of its consequences is currently poorly understood, especially in the persons with metabolic disorders. The aim of the present study was to evaluate the special changes in the cytokines of IL-6 family (IL-6 and sIL-6, LIF and sLIFr), adiponectin and leptin within 360 days after SARS-CoV-2 infection in the patients with metabolic syndrome (MetS), to discern features of immunopathogenesis depending on previous vaccination against COVID-19. We have classified the patients in two groups: (1) patients with MetS who underwent COVID-19 6-12 months after full-course vaccination with a vector vaccine (n = 32); (2) patients with MetS who underwent COVID-19 without story of vaccination (n = 29). Control group included conditionally healthy individuals without MetS: (3) vaccinated, and (4) non-vaccinated, who also had COVID-19. The levels of IL-6 and sIL-6, LIF and sLIFr, leptin and adiponectin, NO, ADMA, SDMA were determined by ELISA technique. In patients with MetS, changes in cytokine regulation towards proinflammatory reactions were revealed (an increase in blood IL-6 and leptin levels), which was most pronounced in MetS within first 30 days post-COVID, but with a number of changes which remained for 12 months (e.g., increased leptin concentration in blood). Vaccination against COVID-19 reduced the severity of pro-inflammatory changes in the sIL- 6r/ IL-6 and leptin/adiponectin systems towards protective adiponectin. However, the persistent increase in leptin was not canceled. When interpreting these results, no negative differences were revealed in the group of once vaccinated individuals with MetS, concerning the mentioned cytokine regulations of MetS over 1 year after COVID-19. The univariate, and then multifactorial correlation analysis between serum contents of sIL- 6r/ IL- 6, LIF/ sLIFr, adiponectin and leptin and the levels of vasoactive substances (NO, ADMA and SDMA), glycated hemoglobin, LDL has shown that the increased ratio of sIL-6r/IL-6 is an independent factor for the NO reduction of (r = 0.74, p 0.01); an increase in sLIFr positively correlates with increase in glycated hemoglobin (r = 0.69, p 0.01), and an association with increase of ADMA (r = 0.82, p 0.001), leptin (in this model) are shown to be an independent factor of LDL increase (r = 0.69, p 0.05). Influence of pre-COVID modifiable factors, in particular, vaccination, is relevant in terms of reducing the likelihood of progression of pre-existing chronic diseases (hypertension, atherosclerosis, diabetes mellitus) in the persons with MetS after COVID-19 and has prospects for implementation into clinical practice.
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