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Does Fluoroscopy Induce DNA Oxidative Damage in Patients Undergoing Catheter Ablation?
Linda Turnu1,2, Benedetta Porro1, Valentina Alfieri1,2
11 Centro Cardiologico Monzino, IRCCS , Milan, Italy .
Antioxidants & Redox Signaling
|September 24, 2017
Summary
This study investigated oxidative and DNA damage from low-dose radiation during catheter ablation (CA). N-acetylcysteine (NAC) reduced glutathione ratio, and 8-hydroxy-2'-deoxyguanosine (8-OHdG) correlated with fluoroscopy time.
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiology
Background:
- Catheter ablation (CA) procedures utilize low-dose ionizing radiation.
- The risks of oxidative and DNA damage from this radiation exposure are not well-understood.
- Investigating these risks is crucial for patient safety during CA.
Purpose of the Study:
- To evaluate oxidative and DNA damage in patients undergoing CA.
- To assess the impact of N-acetylcysteine (NAC) on radiation-induced damage.
- To explore the potential of 8-hydroxy-2 -deoxyguanosine (8-OHdG) as a biomarker.
Main Methods:
- Studied 59 CA patients, with 10 receiving NAC.
- Measured oxidized/reduced glutathione ratio and 8-hydroxy-2 -deoxyguanosine (8-OHdG) levels.
- Assessed DNA tail percentages and correlated with procedure parameters like fluoroscopy time.
Main Results:
- A transient increase in oxidized/reduced glutathione ratio was observed post-CA, mitigated by NAC.
- 8-hydroxy-2 -deoxyguanosine (8-OHdG) peaked 24 hours after CA.
- 8-OHdG levels positively correlated with fluoroscopy time and DNA strand breaks.
Conclusions:
- CA induces oxidative and DNA damage, influenced by radiation exposure.
- N-acetylcysteine (NAC) may offer protective effects against this damage.
- 8-hydroxy-2 -deoxyguanosine (8-OHdG) shows potential as a biomarker for radiation-induced DNA damage.
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