Oxidative stress and DNA damage in critically ill patients with sepsis

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Olgica Mihaljevic , Snezana Zivancevic-Simonovic , Danijela Jovanovic , Svetlana Miletic Drakulic , Jovana Tubic Vukajlovic , Aleksandra Markovic , Marijana Stanojevic Pirkovic , Ivan Srejovic , Vladimir Jakovljevic , Olivera Milosevic-Djordjevic
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Abstract

The aim of our study was to assess the oxidative stress and inflammatory status in critically ill patients with sepsis as well as their relationship with the level of DNA damage. The study also evaluated the influence of all analyzed parameters on the outcome of the patients. The study included 27 critically ill patients with sepsis and 20 healthy subjects. Comet Assay was used for the measurement of the level of DNA damage, expressed as genetic damage index (GDI). Both oxidative stress parameters and the antioxidant parameters were obtained spectrophotometrically. The standard laboratory methods and the appropriate autoanalyzers were performed for determination the parameters of inflammation. A higher level of oxidative stress and more pronounced inflammation were found in the patients with sepsis compared to healthy subjects. The activity of the antioxidant enzymes was statistically declined in patients with sepsis, so that the most notable differences between two groups of participants were found for the activity of superoxide dismutase (SOD) (p = 0.004). Comet assay indicated that patients with sepsis had significantly higher GDI compared to healthy subjects (p < 0.001), which positively correlated with the concentration of superoxide anion radical (О2-) (r = 0.497, p = 0.010), and nitrites (NО2-) (r = 0.473, p = 0.015), as well with the concentration of C reactive protein (CRP) (r = 0.460, p = 0.041). Regression analysis confirmed that patients' age (p = 0.033), the level of О2- (p = 0.007), CRP concentration (p = 0.029) and GDI (p = 0.001) increased the risk of lethal outcome in critically ill patients with sepsis. In conclusion, critically ill patients with sepsis have a higher degree of oxidative stress and inflammation which contribute to a higher level of DNA damage. Consequently, above mentioned parameters, including patients' age, adversely affect the outcome of critically ill patients with sepsis.

危重症脓毒症患者的氧化应激和DNA损伤
我们研究的目的是评估败血症危重患者的氧化应激和炎症状态,以及它们与DNA损伤水平的关系。该研究还评估了所有分析参数对患者结果的影响。该研究包括27名败血症危重患者和20名健康受试者。彗星试验用于测量DNA损伤水平,用遗传损伤指数(GDI)表示。用分光光度法测定了氧化应激参数和抗氧化参数。采用标准实验室方法和适当的自动分析仪测定炎症参数。与健康受试者相比,败血症患者的氧化应激水平更高,炎症更明显。败血症患者的抗氧化酶活性在统计学上下降,因此两组参与者之间的超氧化物歧化酶(SOD)活性存在最显著的差异(p=0.004)。彗星试验表明,败血症患者的GDI明显高于健康受试者(p<;0.001),与超氧阴离子自由基(О2-)浓度(r=0.497,p=0.010)、亚硝酸盐(NО2-,r=0.473,p=0.015)及C反应蛋白(CRP)浓度(r=0.460,p=0.041)呈正相关,CRP浓度(p=0.029)和GDI(p=0.001)增加了败血症危重患者的致死风险。总之,败血症的危重患者具有更高程度的氧化应激和炎症,这会导致更高水平的DNA损伤。因此,上述参数,包括患者的年龄,会对败血症危重患者的预后产生不利影响。
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来源期刊
CiteScore
3.80
自引率
5.30%
发文量
84
审稿时长
105 days
期刊介绍: Mutation Research - Genetic Toxicology and Environmental Mutagenesis (MRGTEM) publishes papers advancing knowledge in the field of genetic toxicology. Papers are welcomed in the following areas: New developments in genotoxicity testing of chemical agents (e.g. improvements in methodology of assay systems and interpretation of results). Alternatives to and refinement of the use of animals in genotoxicity testing. Nano-genotoxicology, the study of genotoxicity hazards and risks related to novel man-made nanomaterials. Studies of epigenetic changes in relation to genotoxic effects. The use of structure-activity relationships in predicting genotoxic effects. The isolation and chemical characterization of novel environmental mutagens. The measurement of genotoxic effects in human populations, when accompanied by quantitative measurements of environmental or occupational exposures. The application of novel technologies for assessing the hazard and risks associated with genotoxic substances (e.g. OMICS or other high-throughput approaches to genotoxicity testing). MRGTEM is now accepting submissions for a new section of the journal: Current Topics in Genotoxicity Testing, that will be dedicated to the discussion of current issues relating to design, interpretation and strategic use of genotoxicity tests. This section is envisaged to include discussions relating to the development of new international testing guidelines, but also to wider topics in the field. The evaluation of contrasting or opposing viewpoints is welcomed as long as the presentation is in accordance with the journal''s aims, scope, and policies.
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