CURRENT ISSUES IN MOLECULAR BIOLOGY, cilt.45, sa.2, ss.963-974, 2023 (SCI-Expanded)
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.