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Published on: February 7, 2018
Oxidative stress as a predictor of cardiovascular events in coronary artery disease patients
Cristina Vassalle1, Sara Bianchi, Fabrizio Bianchi
1Fondazione G.Monasterio CNR-Regione Toscana and Institute of Clinical Physiology-CNR, Pisa, Italy. cristina.vassalle@ftgm.it
Insights
Elevated levels of reactive oxygen metabolites (ROMs) predict worse outcomes in patients with coronary artery disease (CAD). This oxidative stress biomarker can help assess cardiovascular event risk in CAD patients.
Area of Science:
- Cardiology
- Biomarkers
- Oxidative Stress
Background:
- Enhanced oxidative stress is linked to atherosclerosis and coronary artery disease (CAD).
- The predictive value of oxidative stress biomarkers for cardiovascular events (CE) in CAD patients is not well understood.
Purpose of the Study:
- To determine the prognostic significance of serum reactive oxygen metabolites (ROMs) for mortality and major adverse cardiovascular events (MACE) in patients with CAD.
Main Methods:
- A cohort of 93 patients with documented CAD underwent a mean follow-up of 66 months.
- Data on cardiac death, all-cause death, non-fatal myocardial infarction, and revascularization were collected retrospectively.
- Serum ROM levels were measured using a commercial kit.
Main Results:
- Patients with elevated ROM levels (>75th percentile) had significantly worse outcomes.
- Elevated ROMs were a significant predictor of cardiac death (HR 3.9), all-cause death (HR 2.6), and MACE (HR 1.8) in multivariate analysis.
Conclusions:
- Serum ROM estimation can serve as an additional prognostic tool for assessing cardiovascular event risk in CAD patients.
Background:
Enhanced oxidative stress has been associated with atherosclerosis and coronary artery disease (CAD). However, the predictive value of circulating oxidative stress biomarkers for cardiovascular events (CE) in patients with CAD has remained poorly understood.
Aim:
To assess the prognostic significance of reactive oxygen metabolites, estimated as index of oxidative stress in serum samples by means of a commercial kit (ROMs, Diacron, Italy) on the rate of mortality and major adverse CE (MACE) in CAD.
Methods:
A study of 93 consecutive patients with angiographically documented CAD (75 males, age: 68±10 years, mean±SD) was made during a mean follow-up of 66 months until the occurrence of one of the following CE: cardiac and all cause death, non-fatal myocardial infarction and coronary revascularization [percutaneous transluminal coronary angioplasty (PTCA) and coronary artery bypass grafting (CABG)]. Patient data were retrospectively collected from the Institute's electronic databank that saves demographic, clinical, instrumental and follow-up data of all patients admitted to our department.
Results:
The Kaplan-Meier survival estimates showed a significantly worst outcome in patients presenting elevated ROM level (>75th percentile, corresponding to 481 AU) (log rank=11, 7.5, 5.1; p<0.001, p<0.01, p<0.05 for cardiac and all cause death and MACEs, respectively). In a multivariate Cox regression model, elevated oxidative stress remained a significant predictor of cardiac and all cause death [hazard ratio (HR) 3.9, 95% confidence interval, 95% (CI) 1.4-11.1, p=0.01; HR=2.6, 95% CI 1.1-6.2, p=0.02) and MACE (HR=1.8, 95% CI 1.1-3.1, p=0.03)].
Conclusions:
The estimation of ROMs may represent an additional prognostic tool in the assessment of CE in CAD patients.
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