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Published on: May 28, 2013
Phototherapy causes DNA damage in peripheral mononuclear leukocytes in term infants
Ali Aycicek1, Abdurrahim Kocyigit, Ozcan Erel
1Pediatrics Department, Medical Faculty, Harran University, Sanliurfa, Turkey. ayciceka@hotmail.com
Insights
Phototherapy for neonatal jaundice increases DNA damage in infant leukocytes. Both conventional and intensive phototherapy elevate oxidative stress markers, indicating potential cellular harm.
Area of Science:
- Neonatal Medicine
- Molecular Biology
- Biochemistry
Background:
- Neonatal jaundice is common, often treated with phototherapy.
- Phototherapy's potential to induce cellular damage requires investigation.
Purpose of the Study:
- To investigate if phototherapy induces DNA damage in mononuclear leukocytes.
- To assess the correlation between phototherapy, DNA damage, and oxidative stress in jaundiced infants.
Main Methods:
- A comet assay measured DNA damage in 65 term infants (3-10 days old) undergoing intensive or conventional phototherapy.
- Plasma antioxidant capacity, oxidant status, and bilirubin levels were analyzed.
- A control group of 19 infants was included for comparison.
Main Results:
- Infants receiving phototherapy showed significantly higher DNA damage scores compared to controls (p < 0.001).
- Oxidative stress markers (total oxidant status, oxidative stress index) were elevated in phototherapy groups (p = 0.005 and p = 0.041, respectively).
- No significant correlation was found between DNA damage and bilirubin or oxidative stress levels.
Conclusions:
- Both conventional and intensive phototherapy lead to endogenous mononuclear leukocyte DNA damage in jaundiced term infants.
- Phototherapy appears to induce oxidative stress, contributing to DNA damage.
Objective:
Our aim was to determine whether endogenous mononuclear leukocyte DNA strand is a target of phototherapy.
Methods:
The study included 65 term infants aged between 3-10 days that had been exposed to intensive (n = 23) or conventional (n = 23) phototherapy for at least 48 hours due to neonatal jaundice, and a control group (n = 19). DNA damage was assayed by single-cell alkaline gel electrophoresis (comet assay). Plasma total antioxidant capacity and total oxidant status levels were also measured, and correlation between DNA damage and oxidative stress was investigated.
Results:
Mean values of DNA damage scores in both the intensive and conventional phototherapy groups were significantly higher than those in the control group (p < 0.001). Mean values and standard deviation were 32 (9), 28 (9), 21 (7) arbitrary unit, respectively. Total oxidant status levels in both the intensive and conventional phototherapy groups were significantly higher than those in the control group (p = 0.005). Mean (standard deviation) values were 18.1 (4.2), 16.9 (4.4), 13.5 (4.2) micromol H2O2 equivalent/L, respectively. Similarly, oxidative stress index levels in both the intensive and conventional phototherapy groups were significantly higher than those in the control group (p = 0.041). Plasma total antioxidant capacity and total bilirubin levels did not differ between the groups (p > 0.05). There were no significant correlations between DNA damage scores and bilirubin, total oxidant status and oxidative stress levels in either phototherapy group (p > 0.05).
Conclusions:
Both conventional phototherapy and intensive phototherapy cause endogenous mononuclear leukocyte DNA damage in jaundiced term infants.
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