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血清 CCL2 水平低与急性冠状动脉综合征患者预后不良相关:2 年生存分析。

Low serum levels of CCL2 are associated with worse prognosis in patients with Acute Coronary Syndrome: 2-year survival analysis.

机构信息

Departamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Brazil.

Departamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Brazil.

出版信息

Biomed Pharmacother. 2019 Jan;109:1411-1416. doi: 10.1016/j.biopha.2018.10.087. Epub 2018 Nov 12.

Abstract

Inflammation is very important in Acute Coronary Syndrome (ACS) as well as in cardiac remodeling after an acute myocardial infarction (MI). Our study examined the prognostic value of Chemokine (C-C motif) ligand 2 (CCL2) in patients with ACS in the ERICO (Strategy of Registry of Acute Coronary Syndrome) study. We evaluated serum samples from 803 patients. The prognostic value of CCL2 was evaluated at the 2-year follow-up, according to cutoff points established by the median. Kaplan-Meier curves and Cox regression were used for analysis of all-cause mortality, cardiovascular mortality, and a combined outcome of fatal myocardial infarction or new non-fatal MI. There were 115 deaths from all causes, 78 deaths due to cardiovascular causes and 67 events in combined outcomes. CCL2 levels below the median (≤100.9 pg/mL) were associated with increased risk of MI death or new non-fatal MI, even after model adjustment. Low serum levels of CCL2 shows a significant association with fatal or new non-fatal MI.

摘要

炎症在急性冠状动脉综合征(ACS)以及急性心肌梗死(MI)后的心脏重构中非常重要。我们的研究在 ERICO(急性冠状动脉综合征注册策略)研究中检查了趋化因子(C-C 基序)配体 2(CCL2)在 ACS 患者中的预后价值。我们评估了 803 名患者的血清样本。根据中位数确定的截止值,在 2 年随访时评估 CCL2 的预后价值。使用 Kaplan-Meier 曲线和 Cox 回归分析全因死亡率、心血管死亡率和致命性心肌梗死或新发非致命性 MI 的联合结局。有 115 例死于各种原因,78 例死于心血管原因,67 例发生联合结局。CCL2 水平低于中位数(≤100.9pg/mL)与 MI 死亡或新发非致命性 MI 的风险增加相关,即使在模型调整后也是如此。CCL2 血清水平低与致命性或新发非致命性 MI 显著相关。

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