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De Ritis ratio and long-term major cardiovascular adverse events in patients undergoing elective percutaneous
Gjin Ndrepepa1, Stefan Holdenrieder2, Adnan Kastrati1,3
1Deutsches Herzzentrum München, Technical University of Munich, Munich, Germany.
Insights
The De Ritis ratio, an indicator of liver enzyme levels, is linked to increased risks of death and major adverse cardiovascular events in patients with chronic coronary syndromes undergoing PCI. Higher ratios correlate with worse outcomes.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Outcomes
Background:
- The prognostic value of the aspartate aminotransferase to alanine aminotransferase ratio (De Ritis ratio) in chronic coronary syndromes (CCS) is not well-established.
- This study investigates the association between the De Ritis ratio and adverse cardiovascular events in CCS patients.
Purpose of the Study:
- To evaluate the relationship between the De Ritis ratio and long-term adverse cardiovascular events.
- To determine if the De Ritis ratio can predict mortality and other major adverse cardiovascular events in patients with CCS.
Main Methods:
- A cohort of 5020 patients with CCS undergoing percutaneous coronary intervention (PCI) was analyzed.
- Patients were stratified into three groups based on De Ritis ratio tertiles (<.75, .75-1.08, >1.08).
- The primary endpoint was 3-year mortality, with secondary endpoints including myocardial infarction, stroke, and bleeding events.
Main Results:
- Elevated De Ritis ratios were significantly associated with increased 3-year mortality (5.0% vs. 7.5% vs. 14.5%), myocardial infarctions (2.6% vs. 3.5% vs. 5.1%), and strokes (1.0% vs. 1.2% vs. 1.9%).
- Bleeding events at 30 days also showed a significant increase with higher De Ritis ratios (1.4% vs. 1.6% vs. 3.7%).
- Inclusion of the De Ritis ratio improved the predictive accuracy of a Cox proportional hazards model for all-cause mortality (delta C-statistic = .003, p = .005).
Conclusions:
- An elevated De Ritis ratio is a significant predictor of long-term major adverse cardiovascular events in patients with CCS undergoing PCI.
- The De Ritis ratio provides incremental prognostic information beyond traditional risk factors for adverse outcomes in this patient population.
Background:
The association of aspartate aminotransferase to alanine aminotransferase ratio (De Ritis ratio) with clinical outcomes in patients with chronic coronary syndromes (CCS) remains unclear. This study aims to assess the association of De Ritis ratio with adverse cardiovascular events in patients with CCS.
Materials And Methods:
The study included 5020 patients with CCS undergoing percutaneous coronary intervention. Patients were categorized into groups according to tertiles of the De Ritis ratio: tertile 1 (De Ritis ratio: <.75; n = 1688 patients), tertile 2 (De Ritis ratio: .75-1.08; n = 1666 patients) and tertile 3 (De Ritis ratio: >1.08; n = 1666 patients). The primary endpoint was 3-year mortality.
Results:
At 3 years, there were 384 deaths, 176 myocardial infarctions and 61 strokes. In groups with De Ritis in the 1st, 2nd and 3rd tertiles, deaths occurred in 5.0%, 7.5% and 14.5% of the patients, respectively (adjusted hazard ratio = 1.09, 95% confidence interval [1.06-1.12], p < .001); myocardial infarctions occurred in 2.6%, 3.5% and 5.1% of the patients, respectively (p < .001); strokes occurred in 1.0%, 1.2% and 1.9% of the patients, respectively (p = .030); bleeding at 30 days (n = 112) occurred in 1.4%, 1.6% and 3.7% of the patients, respectively (p < .001). The C-statistic of the Cox proportional hazards model for all-cause mortality with baseline data without the De Ritis ratio was .815 [.794-.836] and .818 [.797-.838] after the inclusion of the De Ritis ratio (delta C-statistic = .003; p = .005).
Conclusions:
In patients with CCS undergoing percutaneous coronary intervention, an elevated De Ritis ratio was associated with long-term major adverse cardiovascular events.
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