Association between Oxidative Burden and Restenosis: A Case-Control Study

Shiva Ganjali1, Atena Mansouri2,3, Mitra Abbasifard4,5

  • 1Department of Medical Biotechnology and Nanotechnology, Mashhad University of Medical Sciences, Mashhad, Iran.

Insights

In-stent restenosis (ISR) risk can be predicted by measuring oxidative stress markers. Elevated pro-oxidant-antioxidant balance (PAB) and superoxide dismutase (SOD) activity are associated with increased ISR risk.

Area of Science:

  • Biochemistry
  • Cardiovascular Medicine
  • Oxidative Stress Research

Background:

  • In-stent restenosis (ISR) is a significant complication following stent implantation, with current treatments like drug-eluting stents and medications offering incomplete protection.
  • Identifying patients at high risk for ISR and understanding its biochemical markers are crucial for effective management.
  • Oxidative stress (OS) is a key factor implicated in the development and progression of ISR.

Purpose of the Study:

  • To investigate the association between various oxidative and anti-oxidative markers and the risk of in-stent restenosis (ISR).
  • To identify potential biochemical predictors for ISR risk stratification.
  • To explore the role of oxidative burden in the pathophysiology of ISR.

Main Methods:

  • A case-control study was conducted with 21 ISR patients, 26 non-ISR patients, and 20 healthy controls.
  • Serum levels of malondialdehyde (MDA), thiol groups (GSH), total antioxidant capacity (TAC), glutathione peroxidase (GPx), and superoxide dismutase (SOD) were measured.
  • The pro-oxidant-antioxidant balance (PAB) assay was used to assess the overall oxidative burden.

Main Results:

  • Malondialdehyde (MDA) levels were significantly higher in the ISR group compared to healthy subjects (P=0.004).
  • The pro-oxidant-antioxidant balance (PAB) was significantly elevated in both ISR (P<0.001) and non-ISR (P<0.001) groups versus healthy controls.
  • After adjusting for confounders, elevated PAB (OR: 1.866) and SOD activity (OR: 0.0) were significantly associated with ISR risk, while increased TAC (OR: 0.990) was associated with decreased risk.

Conclusions:

  • Serum markers of oxidative stress, specifically the pro-oxidant-antioxidant balance (PAB) and superoxide dismutase (SOD) activity, show potential for predicting ISR risk.
  • These findings suggest that oxidative stress plays a significant role in the development of ISR.
  • Further research into these markers could lead to improved diagnostic and therapeutic strategies for ISR.
Abstract