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2019冠状病毒病合并糖尿病患者的细胞外氧化应激标志物

Extracellular Oxidative Stress Markers in COVID-19 Patients with Diabetes as Co-Morbidity.

作者信息

Kumar Devika Sanil, Hanumanram Gowtham, Suthakaran Prasanna Karthik, Mohanan Jagadeesan, Nair Lal Devayani Vasudevan, Rajendran Kannan

机构信息

Department of Research and Development, Saveetha Medical College and Hospital, Kancheepuram 602 105, Tamilnadu, India.

Department of General Medicine, Saveetha Medical College and Hospital, Kancheepuram 602 105, Tamilnadu, India.

出版信息

Clin Pract. 2022 Feb 28;12(2):168-176. doi: 10.3390/clinpract12020021.

Abstract

COVID-19 patients have a higher risk of developing inflammatory responses associated with serious and even fatal respiratory diseases. The role of oxidative stress in exacerbating manifestations in COVID-19 pathogenesis is under-reported.This study aimed touseserum levels of superoxide dismutase (SOD3) and glutathione-S-transferase (GSTp1) by ELISA, zinc (ErbaChem5), ferritin and free iron (VitrosChemistry, Ortho Clinical Diagnosis, Raritan, NJ, USA) at the first encounter of randomly selected RT-PCR-positive COVID-19 patients, for assessing disease severity. The parameters which helped in identifying the severity, leading to poor prognosis, were neutrophil:lymphocyte higher than 4, high CRP, low SOD3 values and high GSTp1 values, and diabetes mellitus as a co-morbidity. Higher zinc levels correlated with high GSTp1 and low SOD3, indicating the protective effect of zinc on ROS. The increased high GSTp1 shows an anticipated protective biochemical response, to mitigate the low SOD3 values due to ROS consumption. Decreased SOD3 levels indicate a state of high oxidative stress at cellular levels, and an anticipated increase in GSTp1 levels points to the pathophysiological bases of increasing severity with age, sex, and co-morbidities, such asdiabetes. High levels of initial GSTp1 and zinc levels possibly offer protection to redox reactions at the cellular level in severe COVID-19 infection, preventing deterioration.

摘要

新冠肺炎患者发生与严重甚至致命性呼吸道疾病相关的炎症反应的风险更高。氧化应激在新冠肺炎发病机制中加剧症状方面的作用报道较少。本研究旨在通过酶联免疫吸附测定法检测随机选取的逆转录聚合酶链反应(RT-PCR)阳性新冠肺炎患者初次就诊时血清中超氧化物歧化酶(SOD3)和谷胱甘肽-S-转移酶(GSTp1)的水平,以及锌(ErbaChem5)、铁蛋白和游离铁(Vitros化学检测,美国新泽西州拉里坦市奥瑟临床诊断公司)的水平,以评估疾病严重程度。有助于确定严重程度并导致预后不良的参数包括中性粒细胞与淋巴细胞比值高于4、高C反应蛋白(CRP)、低SOD3值和高GSTp1值,以及合并糖尿病。较高的锌水平与高GSTp1和低SOD3相关,表明锌对活性氧(ROS)有保护作用。高GSTp1水平升高显示出一种预期的保护性生化反应,以减轻因ROS消耗导致的低SOD3值。SOD3水平降低表明细胞水平处于高氧化应激状态,而GSTp1水平预期升高则指出了随着年龄、性别和合并症(如糖尿病)严重程度增加的病理生理基础。在严重的新冠肺炎感染中,初始高GSTp1水平和锌水平可能在细胞水平上为氧化还原反应提供保护,防止病情恶化。

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