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

被引:82
作者
Nunez, Julio [1 ]
Sanchis, Juan [1 ]
Bodi, Vicent [1 ]
Nunez, Eduardo [1 ]
Mainar, Luis [1 ]
Heatta, Anne M. [1 ]
Husser, Oliver [1 ]
Minana, Gema [1 ]
Merlos, Pilar [1 ]
Darmofal, Helene [1 ]
Pellicer, Mauricio [1 ]
Llacer, Angel [1 ]
机构
[1] Univ Valencia, Hosp Clin Univ, Serv Cardiol, Valencia 46010, Spain
关键词
Acute chest pain; Lymphocytes count; All-cause mortality; Myocardial infarction; ST-SEGMENT ELEVATION; BLOOD-CELL COUNT; MYOCARDIAL-INFARCTION; PROGNOSTIC VALUE; UNSTABLE ANGINA; COMPETING RISK; ATHEROSCLEROSIS; LYMPHOPENIA; NEUTROPHIL; PREDICTION;
D O I
10.1016/j.atherosclerosis.2009.01.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 < 0.001), respectively). In a multivariable analysis, patients in lymphocytes' Q1 and Q2 as compared with those in Q4 had an increased risk for the combined endpoint: HR = 2.45 (CI 95% 1.25-4.79, 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. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:251 / 257
页数:7
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