Abiri Elaheh, Abiri Ali, Daneshi Salman, Raesi Rasoul
Department of Cellular and Molecular Biology, School of Biology, Institute of Biological Sciences, Damghan University, Damghan, Iran.
Department of Computer, Da.C., Islamic Azad University, Damghan, Iran.
BMC Infect Dis. 2025 Aug 19;25(1):1041. doi: 10.1186/s12879-025-11419-y.
Persistent symptoms and complications reported by many patients for more than four weeks after contracting coronavirus disease 2019 (COVID-19) are referred to as post-COVID-19 syndrome. These persistent symptoms can occur in individuals with both mild and severe COVID-19, though the underlying pathophysiological mechanisms remain poorly understood. This study aims to explore post-COVID-19 syndrome from a biological perspective, focusing on genomic instability.
In this cross-sectional study, the comet assay method was employed in March 2024 to evaluate the level of DNA damage in 29 patients to examine the post-COVID-19 syndrome state at Kausar Semnan Hospital in Iran. Levels of DNA damage were assessed using the alkaline comet assay in patients hospitalized for COVID-19, four weeks after a positive RT-PCR test. Patients were categorized based on pneumonia severity: mild (11 patients in non-ICU), moderate (10 patients in ICU and non-intubated), and severe/critical (8 patients in ICU and intubated). Ten healthy individuals who tested negative for COVID-19 were considered as a control group. Data were analyzed using descriptive and inferential statistical tests at a significance level of p < 0.01 in GraphPad Prism 9 software.
Post-COVID-19 patients exhibited significantly higher levels of DNA damage compared to healthy controls. The highest DNA damage was observed in intubated-ICU patients (mean DNA damage: 29.5%), followed by non-intubated-ICU patients (mean: 24.3%), non-ICU patients (mean: 19.1%), and healthy controls (mean: 9.4%). These findings suggest a clear correlation between COVID-19 severity and increased genomic instability.
The results of this study highlight the prevalence of DNA damage in post-COVID-19 patients, which may explain long-term genomic instability and associated health complications. The findings underscore the importance of further research into the pathophysiological mechanisms of post-COVID-19 syndrome, particularly its impact on genomic stability. This study contributes to the growing evidence that post-COVID-19 syndrome is a complex condition with virus-specific abnormalities affecting multiple biological pathways. Future studies should focus on understanding these mechanisms to develop targeted interventions for long-term COVID-19 survivors.
许多患者在感染2019冠状病毒病(COVID-19)四周后报告的持续症状和并发症被称为COVID-19后综合征。这些持续症状在轻症和重症COVID-19患者中均可能出现,但其潜在的病理生理机制仍知之甚少。本研究旨在从生物学角度探索COVID-19后综合征,重点关注基因组不稳定性。
在这项横断面研究中,2024年3月采用彗星试验法评估了伊朗考萨尔塞姆南医院29例患者的DNA损伤水平,以检查COVID-19后综合征状态。在RT-PCR检测呈阳性四周后,对因COVID-19住院的患者使用碱性彗星试验评估DNA损伤水平。患者根据肺炎严重程度进行分类:轻症(11例非重症监护病房患者)、中症(10例重症监护病房且未插管患者)和重症/危重症(8例重症监护病房且插管患者)。10例COVID-19检测呈阴性的健康个体被视为对照组。在GraphPad Prism 9软件中使用描述性和推断性统计检验对数据进行分析,显著性水平为p < 0.01。
与健康对照组相比,COVID-19后患者的DNA损伤水平显著更高。插管的重症监护病房患者的DNA损伤最高(平均DNA损伤:29.5%),其次是非插管的重症监护病房患者(平均:24.3%)、非重症监护病房患者(平均:19.1%)和健康对照组(平均:9.4%)。这些发现表明COVID-19严重程度与基因组不稳定性增加之间存在明显关联。
本研究结果突出了COVID-19后患者中DNA损伤的普遍性,这可能解释了长期的基因组不稳定性及相关健康并发症。这些发现强调了进一步研究COVID-19后综合征病理生理机制的重要性,特别是其对基因组稳定性的影响。本研究为越来越多的证据做出了贡献,即COVID-19后综合征是一种复杂病症,具有影响多种生物学途径的病毒特异性异常。未来的研究应专注于理解这些机制,以便为长期COVID-19幸存者开发针对性干预措施。