Predictive value of neutrophil-to-lymphocyte ratio in coronary chronic total occlusion patients.
J Geriatr Cardiol
; 21(5): 542-549, 2024 May 28.
Article
en En
| MEDLINE
| ID: mdl-38948892
ABSTRACT
BACKGROUND:
The neutrophil to lymphocyte ratio (NLR) has been reported as a novel predictor for atherosclerosis and cardiovascular outcomes. This study aimed to determine the effects of NLR on long-term clinical outcomes of chronic total occlusion (CTO) patients.METHODS:
A total of 670 patients with CTO who met the inclusion criteria were included at the end of the follow-up period. Patients were divided into tertiles according to their baseline NLR levels at admission low (n = 223), intermediate (n = 223), and high (n = 224). The incidence of major adverse cardiac events (MACEs) during the follow-up period, including all-cause death, nonfatal myocardial infarction (MI), or ischemia-driven revascularization, were compared among the three groups.RESULTS:
Major adverse cardiac events were observed in 27 patients (12.1%) in the low tertile, 40 (17.9%) in the intermediate tertile, and 61 (27.2%) in the high NLR tertile (P < 0.001). Kaplan-Meier analysis demonstrated a significantly higher incidence of MACE, ischemia-driven coronary revascularization, non-fatal MI, and mortality in patients within the high tertile than those in the low and intermediate groups (all P < 0.001). Multivariable COX regression analysis showed that the high tertile of baseline NLR level showed a strong association with the risk of MACE (hazard ratio [HR] = 2.21; 95% confidence interval [CI] 1.21-4.03; P = 0.009), ischemia-driven coronary revascularization (HR = 3.19; 95% CI 1.56-6.52; P = 0.001), MI (HR = 2.61; 95% CI 1.35-5.03; P = 0.043) and mortality (HR = 3.78; 95% CI 1.65-8.77; P = 0.001).CONCLUSION:
Our findings suggest that NLR is an inexpensive and readily available biomarker that can independently predict cardiovascular risk in patients with CTO.
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Colección:
01-internacional
Base de datos:
MEDLINE
Idioma:
En
Revista:
J Geriatr Cardiol
Año:
2024
Tipo del documento:
Article
País de afiliación:
China
Pais de publicación:
China