The Influence of Reactive Oxygen Species in the Development of Contrast-Induced Nephropathy After Coronary Angiography

<b>Background/Objectives</b>: Contrast agents can damage renal tissue through multiple mechanisms, particularly by increasing reactive oxygen species (ROS), which contribute to DNA oxidation, lipid peroxidation, and endothelial injury. This prospective, comparative study aimed to evaluate the changes in ROS-related gene expressions-<i>NFKB1</i>, <i>SIRT1</i>, <i>NFE2L2</i>, and <i>FOXO1</i>-in patients who developed contrast-induced nephropathy (CIN) following coronary angiography versus those who did not. <b>Methods</b>: A total of 48 patients undergoing primary percutaneous coronary intervention were enrolled. Twenty-three patients who developed CIN (Group 1) were compared to 25 matched controls without CIN (Group 2) based on age, gender, and comorbidities. Blood and serum samples were collected 72 h post-contrast exposure to assess biochemical markers and mRNA expression levels of the target genes. <b>Results</b>: The mean age was similar between the groups (63 ± 7 vs. 62 ± 6 years; <i>p</i> > 0.05), as was gender distribution. Group 1 showed significant increases in serum creatinine and reductions in e-GFR post-procedure. Importantly, <i>NFKB1</i>, <i>NFE2L2</i>, and <i>FOXO1</i> mRNA expression levels were significantly upregulated in CIN patients-by 5.7-, 5.8-, and 4.97-fold, respectively, while <i>SIRT1</i> expression was downregulated by 0.76-fold (<i>p</i> < 0.05). <b>Conclusions</b>: These findings indicate enhanced activation of inflammatory and oxidative stress pathways in CIN patients, particularly through the NF-κB signaling axis. Conversely, reduced <i>SIRT1</i> expression suggests diminished antioxidant protection. The study highlights that ROS-related gene expression changes may serve as potential biomarkers for CIN progression. Further studies at the protein level are needed to clarify cytokine roles in these pathways.