Relationship between low lymphocyte count and major cardiac events in patients with acute chest pain, a non-diagnostic electrocardiogram and normal troponin levels

医学 心肌梗塞 内科学 心脏病学 肌钙蛋白 急性冠脉综合征 人口 临床终点 四分位数 胸痛 淋巴细胞 置信区间 环境卫生 临床试验
作者
Julio Núñez,Juan Sanchís,Vicent Bodı́,Eduardo Núñez,Luis Mainar,Anne M. Heatta,Oliver Hüsser,Gema Miñana,Pilar Merlos,Helene Darmofal,Mauricio Pellicer,Ángel Llácer
出处
期刊:Atherosclerosis [Elsevier BV]
卷期号:206 (1): 251-257 被引量:94
标识
DOI:10.1016/j.atherosclerosis.2009.01.029
摘要

Abstract Objective Risk stratification of patients with acute chest pain, non-diagnostic electrocardiogram and normal troponin (ACPneg) remains a challenge, partly because no standardized set of biomarkers with prognostic ability has been identified in this population. Lymphopenia has been associated with atherosclerosis progression and adverse outcomes in cardiovascular diseases; although its prognostic value in ACPneg is unknown. We sought to determine the relationship between the lymphocyte count obtained in the Emergency Department (ED) and the risk of the long-term all-cause mortality or myocardial infarction (MI) in patients with ACPneg. Methods We analyzed 1030 consecutive patients admitted with ACPneg in our institution. Lymphocyte count was determined in the ED as a part of a routine diagnostic workup to rule out an acute coronary syndrome. Patients with inflammatory, infectious diseases, or active malignancy were excluded (final sample=975). The independent association between lymphocyte count and the composite endpoint (death/MI) was assessed by survival analysis for competing risk events (revascularization procedures). Results During a median follow-up of 36 months, 139 (14.3%) patients achieved the combined endpoint, with rates increasing monotonically across lymphocyte quartiles (6.2%, 10%, 20.6% and 24.1% for Q4, Q3, Q2 and Q1 ( p p =0.008) and HR=2.56 (CI 95% 1.30–5.07, p =0.007), respectively. Conclusion In patients with ACPneg, low lymphocytes count was associated with an increased risk for developing the combined endpoint of death or MI.
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