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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Determinants and prognostic significance of collaterals in patients undergoing coronary revascularization
Hendrik M Nathoe1, Jeroen Koerselman, Erik Buskens
1Department of Cardiology, Heart Lung Center Utrecht, Utrecht.
Insights
Coronary collaterals significantly reduce the risk of cardiac death and myocardial infarction (MI) by 1 year after revascularization in patients with stable coronary artery disease. Their presence is determined by factors reflecting the severity of atherosclerosis and ischemia.
Area of Science:
- Cardiology
- Vascular Biology
- Interventional Cardiology
Background:
- Coronary collaterals are known to improve prognosis in acute myocardial infarction (MI).
- Limited clinical data exists on the protective role of collaterals in stable coronary artery disease (CAD).
- Understanding collateral function aids risk stratification and development of therapies like arteriogenesis and angiogenesis.
Purpose of the Study:
- To investigate the relationship between coronary collateral status and the risk of cardiac death or MI at 1 year post-coronary revascularization.
- To identify independent determinants of coronary collateral presence in patients with stable CAD.
Main Methods:
- A randomized study comparing stent implantation with bypass grafting in 561 patients.
- Coronary collaterals assessed via Rentrop's classification on angiograms (grade >1 considered present).
- Univariate and multivariate regression analyses used to calculate odds ratios for outcomes and determinants.
Main Results:
- Collateral blood flow was present in 31% of patients (176/561).
- Presence of collaterals was associated with a significantly reduced adjusted odds ratio of 0.18 for cardiac death or MI at 1 year.
- Independent determinants included age, multivessel disease, impaired ventricular function, type C lesion, and stenosis severity >90%.
Conclusions:
- Coronary collaterals offer significant protection against cardiac death and MI within one year following coronary revascularization in patients with a low-risk profile.
- The development of coronary collaterals is influenced by the duration and severity of atherosclerotic and ischemic burden.
Abstract:
There is evidence that coronary collaterals improve the prognosis in patients with acute myocardial infarction (MI). However, there is limited clinical information on the protective role of collaterals in patients with stable coronary artery disease. This information may help risk stratification and the development of novel therapies, such as arteriogenesis and angiogenesis. The relation between collaterals and cardiac death or MI at 1 year after coronary revascularization was studied in 561 patients who were enrolled in a randomized study that compared stent implantation with bypass grafting. Collaterals were assessed on an angiogram using Rentrop's classification and considered present with a Rentrop grade >1. Unadjusted and adjusted odds ratios for cardiac death or MI at 1 year were calculated using univariate and multivariate regression analyses. In addition, determinants of collaterals were assessed using univariate and multivariate analyses. Collaterals were present in 176 patients (31%). The adjusted odds ratio of cardiac death or infarction was 0.18 (95% confidence interval 0.04 to 0.78) in the presence of collaterals. Independent determinants of collaterals were age (odds ratio 0.97, 95% confidence interval 0.95 to 0.99), multivessel disease (odds ratio 1.60, 95% confidence interval 1.02 to 2.51), impaired ventricular function (odds ratio 1.85, 95% confidence interval 1.04 to 3.29), type C lesion (odds ratio 3.72, 95% confidence interval 2.33 to 5.95), and stenosis severity >90% (odds ratio 9.08, 95% confidence interval 4.65 to 17.73). In conclusion, in patients with a low risk profile, the presence of collaterals protects against cardiac death and MI at 1 year after coronary revascularization. Variables that reflect the duration and severity of the atherosclerotic and ischemic burden determine their presence.
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