The silent legacy of COVID-19: exploring genomic instability in long-term COVID-19 survivors by Elaheh Abiri1 , Ali Abiri2, Salman Daneshi3 and Rasoul Raesi instant download

The silent legacy of COVID-19: exploring genomic instability in long-term COVID-19 survivors by Elaheh Abiri1 , Ali Abiri2, Salman Daneshi3 and Rasoul Raesi instant download

Background 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.

Methods 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.

Results 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.

Conclusion 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 syndro