C-X-C配体16是急性冠状动脉综合征心血管死亡和发病率的独立预测因子

T. Andersen, T. Ueland, T. Ghukasyan Lakic, A. Åkerblom, M. Bertilsson, P. Aukrust, A. Michelsen, S. James, R. Becker, R. Storey, L. Wallentin, A. Siegbahn, F. Kontny
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引用次数: 23

摘要

目的CXCL16(趋化因子C-X-C基模配体16)是氧化低密度脂蛋白(OxLDL)的清除率受体,参与动脉粥样硬化部位的炎症。本研究旨在探讨CXCL16与急性冠脉综合征患者临床预后的关系。方法和结果:在PLATO试验(血小板抑制和患者结局)中随机分配的5142例患者亚组中进行了CXCL16的一系列测量。通过多变量Cox回归分析评估CXCL16与心血管死亡、自发性心肌梗死或卒中的组合以及单个成分之间的相关性。作为连续变量分析的CXCL16入院水平每增加50%的风险比为1.64 (95% CI, 1.44-1.88), P<0.0001。在调整随机治疗、临床变量、CRP (C反应蛋白)、白细胞、胱抑素C、NT-proBNP (n端前脑利钠肽)、肌钙蛋白T、GDF-15(生长分化因子15)和其他生物标志物后,这种关联仍具有统计学意义;风险比1.23 (1.05 ~ 1.45),P=0.0126。在完全校正分析中,CXCL16的入院水平与心血管死亡独立相关(1.50 [1.17-1.92],P=0.0014),但与单独的缺血性事件无关。在1个月时测量的CXCL16或入院至1个月时CXCL16的变化与临床结果之间没有统计学上独立的关联。结论在急性冠脉综合征患者中,CXCL16的入院水平与不良临床结局独立相关,主要与心血管死亡相关。因此,测量CXCL16可能会增强这种疾病患者的风险分层。临床试验注册网址:http://www.clinicaltrials.gov。唯一标识符:NCT00391872。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C-X-C Ligand 16 Is an Independent Predictor of Cardiovascular Death and Morbidity in Acute Coronary Syndromes.
OBJECTIVE The CXCL16 (chemokine C-X-C motif ligand 16) is a scavenger receptor for OxLDL (oxidized low-density lipoproteins) and involved in inflammation at sites of atherosclerosis. This study aimed to investigate the association of CXCL16 with clinical outcome in patients with acute coronary syndrome. Approach and Results: Serial measurements of CXCL16 were performed in a subgroup of 5142 patients randomized in the PLATO trial (Platelet Inhibition and Patient Outcome). Associations between CXCL16 and a composite of cardiovascular death, spontaneous myocardial infarction or stroke, and the individual components were assessed by multivariable Cox regression analyses. The hazard ratio per 50% increase in admission levels of CXCL16 analyzed as continuous variable was 1.64 (95% CI, 1.44-1.88), P<0.0001. This association remained statistically significant after adjustment for randomized treatment, clinical variables, CRP (C-reactive protein), leukocytes, cystatin C, NT-proBNP (N-terminal pro-brain natriuretic peptide), troponin T, GDF-15 (growth differentiation factor 15), and other biomarkers; hazard ratio 1.23 (1.05-1.45), P=0.0126. The admission level of CXCL16 was independently associated with cardiovascular death (1.50 [1.17-1.92], P=0.0014) but not with ischemic events alone, in fully adjusted analyses. No statistically independent association was found between CXCL16 measured at 1 month, or change in CXCL16 from admission to 1 month, and clinical outcomes. CONCLUSIONS In patients with acute coronary syndrome, admission level of CXCL16 is independently related to adverse clinical outcomes, mainly driven by an association to cardiovascular death. Thus, CXCL16 measurement may enhance risk stratification in patients with this condition. CLINICAL TRIAL REGISTRATION URL: http://www.clinicaltrials.gov. Unique identifier: NCT00391872.
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