The Monocyte-to-Lymphocyte Ratio Exhibits A Superior Prognostic Value in Patients with Newly Diagnosed Acute Coronary Syndrome
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Updated: Jan 11, 2026

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Published on: January 28, 2020
Mi Lao1,2, Huiling Liu3, Xiaoping Cai3
1Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, The Second Hospital of Tianjin Medical University, 300211 Tianjin, China.
Insights
The monocyte-to-lymphocyte ratio (MLR) effectively predicts major adverse cardiovascular events (MACEs) in acute coronary syndrome (ACS) patients. Elevated MLR indicates a significantly higher risk, suggesting its use in cardiovascular risk assessment.
Area of Science:
- Cardiology
- Inflammation Research
- Biomarker Discovery
Background:
- Chronic inflammation is a key driver of atherosclerosis and plaque instability.
- Lymphocyte-derived inflammatory indices are investigated for their prognostic value in cardiovascular diseases.
Purpose of the Study:
- To compare six lymphocyte-derived inflammatory indices for predicting major adverse cardiovascular events (MACEs) in treatment-naïve acute coronary syndrome (ACS) patients.
- To evaluate the monocyte-to-lymphocyte ratio (MLR) as a predictive biomarker for MACEs in ACS.
Main Methods:
- 1120 newly diagnosed ACS patients were enrolled, with MACEs monitored over a median follow-up of 64.20 months.
- Predictive capacities of inflammatory indices were assessed using receiver operator characteristic (ROC) curve analysis and Cox proportional hazards modeling.
Main Results:
- An elevated monocyte-to-lymphocyte ratio (MLR) was independently associated with a higher risk of MACEs (HR = 2.880).
- MLR demonstrated superior discriminative capacity compared to clinical factors, with an optimal cutoff of 0.304.
- Patients with high MLR (≥0.304) had a 3.5-fold increased risk of MACEs, with consistent prognostic value across high-risk subgroups.
Conclusions:
- The monocyte-to-lymphocyte ratio (MLR) is a robust and superior biomarker for predicting MACEs in ACS patients.
- MLR can be integrated into routine cardiovascular risk assessment protocols for improved patient stratification.
Background:
Chronic inflammation critically influences atherosclerotic progression and plaque destabilization. This investigation assessed and compared six lymphocyte-derived inflammatory indices (neutrophil-to-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), platelet-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), systemic inflammatory response index (SIRI), systemic immune-inflammation response index (SIIRI)) for predicting major adverse cardiovascular events (MACEs) in treatment-naïve acute coronary syndrome (ACS) patients undergoing coronary angiography.
Methods:
This study enrolled 1120 patients with newly diagnosed ACS, in which the occurrence of MACEs was monitored. The predictive capacities of the included lymphocyte-derived inflammatory indices were evaluated through receiver operator characteristic (ROC) curve analysis with optimal cutoffs, supplemented by Cox proportional hazards modeling.
Results:
A total of 265 MACEs (23.66%) were recorded during the 64.20 ± 23.05-month follow-up. Multivariate Cox analyses identified an elevated MLR (hazard ratio (HR) = 2.880, 95% confidence interval (CI) 1.280-6.470; p < 0.001) that was independently associated with the occurrence of MACEs in patients with newly diagnosed ACS. The ROC comparisons revealed a superior discriminative capacity of the MLR versus clinical factors, with an optimal MLR cutoff at 0.304 (sensitivity 61.1%; specificity 78.8%). Patients with a high MLR (≥0.304) exhibited a 3.5-fold increased risk of MACEs compared to those with a low MLR (46.96% vs. 13.29%; risk ratio = 1.635, 95% CI 1.475-1.812; p < 0.001); these data were corroborated by divergent Kaplan-Meier curves (log-rank p < 0.001). Meanwhile, subgroup analyses confirmed the prognostic consistency of the MLR across high-risk populations (age >60 years, diabetes, hypertension), with elevated MLR subgroups demonstrating uniformly higher rates of MACEs (all p < 0.001).
Conclusions:
MLR outperformed conventional parameters and five novel lymphocyte-based inflammatory indices in predicting MACEs in ACS patients; thus, the MLR can be established as a robust predictive biomarker. The clinical utility of the MLR extends to risk stratification across key patient subgroups, suggesting potential integration into routine cardiovascular risk assessment protocols.
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