用碱性彗星试验评估系统性红斑狼疮妇女的 DNA 损伤与临床结果无关

Camila De Melo Carvalho Nascimento, L. Alves, Rodrigo Cutrim Gaudio, Alice Ramos Silva, Matheus Daudt Lemos, M. Cabral-Castro, Katia Lino Batista, Ana Luísa Figueira Gouvêa, Jorge Reis Almeida, Andrea Alice da Silva, Thalia Medeiros, Fabiana Rabe Carvalho
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摘要

在系统性红斑狼疮(SLE)中,炎症状态导致氧化应激和活性氧的过度形成,增加细胞损伤、突变和DNA修复受损。因此,我们的研究旨在评估碱性彗星试验在SLE女性DNA损伤研究中的性能。方法:这是一项横断面研究,包括2015年至2018年在一家大学医院(巴西里约热内卢)就诊的SLE巴西女性。采用SLE疾病活动性指数2000 (SLEDAI-2K)评估疾病活动性。采用qPCR方法诊断cmv和EBV感染。DNA损伤是通过碱性彗星法测定的,这是一种用于评估白细胞DNA片段的电泳技术,以任意单位(AU)表达。结果:我们研究了34例SLE患者,中位年龄34.5岁。住院患者SLEDAI-2K较高(n=11, 32.3%),其中SLEDAI-2K≥5者9例(81.8%)(p=0.038)。我们没有发现健康和SLE之间的显著差异;住院患者中位AU较高,但差异无统计学意义(p=0.095)。此外,根据SLEDAI-2、狼疮肾炎、使用免疫抑制剂或CMV/EBV感染,DNA损伤也没有差异。DNA损伤与抗dsdna水平无关。最后,ROC曲线显示DNA损伤对不同组的预测能力较差(AUC < 0.7, p > 0.05)。结论:我们的研究结果表明,碱性彗星法测量的DNA损伤与SLE严重程度和病毒感染的存在无关
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE ASSESSMENT OF DNA DAMAGE BY ALKALINE COMET ASSAY IS NOT ASSOCIATED WITH CLINICAL OUTCOMES IN WOMEN WITH SYSTEMIC LUPUS ERYTHEMATOSUS
Introduction: In systemic lupus erythematosus (SLE), an inflammatory state leads to oxidative stress and excessive formation of reactive oxygen species, increasing cellular damage, mutations and compromised DNA repair. Therefore, our study aimed to evaluate the performance of the alkaline comet assay to investigate DNA damage in women with SLE.Methods: This is a cross-sectional study that included Brazilian women with SLE attended at an university hospital (Rio de Janeiro, Brazil) from 2015 to 2018. Disease activity was assessed using the SLE Disease Activity Index 2000 (SLEDAI-2K). Diagnosis of CMVand EBV infections were performed by qPCR. DNA damage was determined by alkaline comet assay, which is a electrophoresis techinique used to evaluate DNA fragmentation in leukocytes, which is expressed as arbitrary units (AU). Results: We studied 34 SLE patients with a median age of 34.5 years-old. Hospitalized patients (n=11, 32.3%) presented higher SLEDAI-2K, where 9 (81.8%) had SLEDAI-2K ≥ 5 (p=0.038). We did not identify significant differences between healthy and SLE; however, hospitalized patients showed higher median AU, but with no statistical significance (p=0.095). Also, no differences were in DNA damage according to SLEDAI-2, lupus nephritis, use of immunossupressants, or CMV/EBV infections. DNA damage was not associated with levels of anti-dsDNA. Lastlty, ROC curves demonstrated a poor predictive power of DNA damage to differentiate groups (AUC < 0.7, p > 0,05). Conclusion: Our results indicate that DNA damage measured by alkaline comet assay is not associated with SLE severity and the presence of viral infections
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