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American Heart Association

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Final ID: Sa1065

Neutrophil-lymphocyte ratio as a marker of cardiovascular outcomes in patients with chronic coronary syndrome

Abstract Body (Do not enter title and authors here): Background: Inflammation is one of the pathophysiological processes involved in the genesis and progression of atherosclerosis and has been increasingly used as a therapeutic target in recent years. The neutrophil-lymphocyte ratio (NLR) is a promptly accessible inflammatory biomarker strongly associated with prognosis in the acute coronary setting. However, there are few data in patients with chronic coronary syndrome (CCS).
Objective: Analyze the association between NLR and cardiovascular outcomes in patients with CCS.
Methods: Patients with CCS, defined as a previous revascularization procedure (surgical or percutaneous), previous myocardial infarction (MI) or stenosis > 50% in at least one epicardial coronary artery, were included and followed up on an outpatient basis. The NLR was calculated using the baseline blood count. The main outcome was the composite of death, non-fatal myocardial infarction and non-fatal stroke.
Results: The study population consisted of 975 patients, with a median age of 65 years and 30% were women. Previous MI was present in 61%, 30% had undergone previous revascularization surgery and 46% had percutaneous coronary intervention. Diabetes was prevalent in 59% and hypertension in 95%. The median NLR was 2.15 (IQR 1.25 - 2.87). Patients with NLR ≥ 2.15, when compared to those with NLR < 2.15, presented more left ventricular (LV) dysfunction (58% vs. 55%; p=0.003) and lower LDL-C serum levels (81 vs. 88 mg/dL; p=0.004). There was no association between NLR and coronary anatomical severity. NLR correlated with age, LDL-C and LV function (p < 0.05 for all). During follow-up, 152 events of the composite primary outcome were registered, with an estimated 3-year incidence of 15.6% in the overall population – higher within patients with NLR ≥ 2.15 when compared to NLR < 2.15 (20% x 14%, p = 0.002), as shown in the figure. In the multivariate analysis, the 3rd quartile of NLR had a 31% higher risk than the 1st quartile (p < 0.05).
Conclusion: In this study, the NLR, an easily available inflammatory biomarker, independently correlates with cardiovascular outcomes in a population with CCS.
  • Trombini Pinesi, Henrique  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Moreira, Eduardo  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Barbosa, Marcelo  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Martins, Eduardo  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Pitta, Fabio Grunspun  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Lima, Eduardo  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Rached, Fabiana Hanna  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Serrano, Carlos  ( Instituto do Coracao, Hospital das Clinicas, Faculdade de Medicina, Universidade de Sao Paulo , Sao Paulo , Brazil )
  • Author Disclosures:
    Henrique Trombini Pinesi: DO NOT have relevant financial relationships | Eduardo Moreira: No Answer | Marcelo Barbosa: No Answer | Eduardo Martins: No Answer | FABIO GRUNSPUN PITTA: DO NOT have relevant financial relationships | Eduardo Lima: No Answer | FABIANA HANNA RACHED: DO NOT have relevant financial relationships | Carlos Serrano: DO NOT have relevant financial relationships
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Inflammation in Cardiovascular and Metabolic Disease

Saturday, 11/16/2024 , 02:00PM - 03:00PM

Abstract Poster Session

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