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Clinical Investigation of Leukocyte DNA Damage in COVID-19 Patients
Hasan Doğan1, Aslı Kara2, Erdem Çankaya3
1Department of Medical Biology, Faculty of Medicine, Ataturk University, Erzurum 25240, Turkey.
Insights
COVID-19 infection significantly increases leukocyte DNA damage, indicated by higher tail and olive moments in patients. The neutrophil/lymphocyte ratio also correlates with disease presence and progression.
Area of Science:
- Biochemistry
- Genetics
- Immunology
Background:
- Coronavirus disease (COVID-19) is a global health crisis with complex pathophysiological mechanisms.
- Understanding cellular and molecular changes associated with COVID-19 is crucial for diagnosis and treatment.
- Leukocyte DNA integrity may be affected during viral infections.
Purpose of the Study:
- To evaluate leukocyte DNA damage in patients with COVID-19.
- To compare DNA damage markers between COVID-19 patients and a control group.
- To investigate the correlation between hematological parameters, DNA damage, and COVID-19.
Main Methods:
- Prospective cross-sectional study involving 50 COVID-19 patients and 42 controls.
- Leukocyte DNA damage assessed using the comet assay, measuring tail and olive moments.
- Analysis of various hematological parameters including white blood cells, red blood cells, hemoglobin, and neutrophil/lymphocyte ratio (NLR).
Main Results:
- COVID-19 patients exhibited significantly higher tail and olive moments, indicating increased DNA damage.
- Significant negative correlations were observed between COVID-19 and red blood cells, lymphocytes, eosinophils, and monocytes.
- Positive correlations were found between COVID-19 and hemoglobin, neutrophils, tail moment, and olive moment. The NLR was associated with disease presence and progression.
Conclusions:
- COVID-19 infection causes statistically significant DNA damage in leukocytes.
- Hematological parameters like hemoglobin and neutrophil counts are elevated in COVID-19 patients.
- The neutrophil/lymphocyte ratio is a relevant marker for COVID-19 presence and progression, alongside observed DNA damage.
Abstract:
This prospective cross-sectional study aimed to evaluate leukocyte DNA damage in coronavirus disease (COVID-19) patients. In this study, 50 COVID-19-positive patients attending the Erzurum City Hospital Internal Medicine Outpatient Clinic and 42 control group patients were included. DNA damage was detected in living cells through leukocyte isolation in 50 COVID-19-positive patients using the comet assay method. DNA tail/head (olive) moments were evaluated and compared. White blood cells (WBC), red blood cells (RBC), hemoglobin (HGB), neutrophils (NEU), lymphocytes (LYM), eosinophils (EO), monocytes (MONO), basophils (BASO), platelets (PLT), and the neutrophil/lymphocyte ratio (NLR) were analyzed. The RBC, lymphocyte, eosinophil, and monocyte means were significantly higher in the control group (p < 0.05), whereas the HGB and neutrophile means were significantly higher in the study group (p < 0.05). There were significant negative correlations between COVID-19 and RBC (r = -0.863), LYM (r = -0.542), EO (r = -0.686), and MONO (r = -0.385). Meanwhile, there were significant positive correlations between COVID-19 and HGB (r = 0.863), NEU (r = 0.307), tail moment (r = 0.598), and olive moment (r = 0.582). Both the tail and olive moment mean differences were significantly higher in the study group, with higher ranges (p < 0.05). COVID-19 infection caused statistically significant increases in both the tail and olive damage percentage in patients, causing DNA damage. Lastly, the NLR rate was associated with the presence and progression of COVID-19.
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