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Published on: June 5, 2014
Jaundice, phototherapy and DNA damage in full-term neonates
N Ramy1, E A Ghany1, W Alsharany1
1Pediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Insights
Phototherapy for neonatal jaundice increases DNA damage in infants, with longer treatment durations correlating to greater harm. Neonatal jaundice itself does not appear to affect DNA damage levels.
Area of Science:
- Neonatal Medicine
- Genetics
- Biochemistry
Background:
- Phototherapy is a standard treatment for neonatal hyperbilirubinemia.
- Concerns exist regarding potential oxidative DNA damage from phototherapy.
- Unconjugated bilirubin (UCB) may possess protective antigenotoxic properties.
Purpose of the Study:
- To evaluate the effects of neonatal hyperbilirubinemia on DNA damage.
- To compare DNA damage in infants receiving conventional versus intensive phototherapy.
- To assess DNA damage in peripheral blood mononuclear cells (PBMCs).
Main Methods:
- Study included term neonates with non-hemolytic hyperbilirubinemia and healthy controls.
- Genotoxicity assessed using the single-cell gel electrophoresis (Comet assay).
- Blood samples collected pre- and post-phototherapy.
Main Results:
- No significant difference in DNA damage between jaundiced and non-jaundiced neonates.
- Phototherapy significantly increased DNA damage compared to pre-treatment levels (P<0.001).
- Phototherapy duration positively correlated with DNA damage (r=0.86, P<0.001); intensity did not significantly impact genotoxicity.
Conclusions:
- Neonatal hyperbilirubinemia does not influence DNA damage.
- Both conventional and intensive phototherapy are associated with increased DNA damage in term infants.
- Findings highlight the genotoxic potential of phototherapy in neonates.
Objective:
Phototherapy is the standard therapeutic approach for neonatal hyperbilirubinemia. Oxidative effects of phototherapy may have potential harms, including DNA damage. Unconjugated bilirubin (UCB) might also possess antigenotoxic potential. Intensive phototherapy is more efficacious than conventional phototherapy in treating hyperbilirubinemia. This study aimed to assess the impact of hyperbilirubinemia and the two different types of phototherapy on DNA damage in peripheral blood mononuclear cells of neonates.
Study Design:
The study was conducted on term neonates with non-hemolytic hyperbilirubinemia and control healthy neonates. Genotoxicity was assessed using single-cell gel electrophoresis (Comet assay) in peripheral mononuclear cells. Blood samples were obtained at enrollment in all infants and after intensive or conventional phototherapy in jaundiced infants.
Result:
DNA damage did not significantly differ between jaundiced and non-jaundiced neonates (11.4±8.7 and 10.9±8.3 arbitrary units (AU), respectively, P=0.58). It increased significantly after exposure to phototherapy compared with prephototherapy values (45.6±14.7 vs 11.4±8.7 AU, respectively, P<0.001). The duration of phototherapy correlated positively with markers of DNA damage (r=0.86, P<0.001); however, the intensity of used light did not significantly impact genotoxicity.
Conclusion:
Hyperbilirubinemia does not influence DNA damage, whereas both conventional and intensive phototherapy are associated with DNA damage in term infants with hyperbilirubinemia.
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