Ray Kausik K, Morrow David A, Sabatine Marc S, Shui Amy, Rifai Nader, Cannon Christopher P, Braunwald Eugene
Department of Public Health and Primary Care, University of Cambridge, Worts Causeway, Cambridge, CB1 8RN, United Kingdom.
Circulation. 2007 Jun 19;115(24):3071-8. doi: 10.1161/CIRCULATIONAHA.106.666511. Epub 2007 Jun 4.
Monocyte activation is believed to play an important role in the pathogenesis of acute coronary syndromes (ACS). Neopterin is a soluble marker of monocyte activation, and elevated levels are of prognostic value in patients with stable coronary artery disease.
Neopterin levels were measured on average at 7 days (in 3946 patients) and at 4 months (in 3369 patients) after ACS in the PRavastatin Or atorVastatin Evaluation Infection Therapy-Thrombolysis In Myocardial Infarction (PROVE IT-TIMI 22) trial. We assessed the relationship between plasma neopterin levels and the risk of death and death or acute coronary events (nonfatal myocardial infarction or unstable angina) over 2 years. Seven days after an ACS event, neopterin levels > or = 12.11 nmol/L (upper quartile, derived from a post hoc analysis) were associated with an increased risk of death and an increased risk of death or acute coronary events after adjustment for age, gender, history of diabetes mellitus, history of hypertension, history of smoking, type of ACS presentation, use of percutaneous coronary intervention for the index event, statin regimen, low-density lipoprotein cholesterol, and high-sensitivity C-reactive protein (hazard ratio, 1.86 [95% CI, 1.24 to 2.77], P=0.003; and hazard ratio, 1.33 [95% CI, 1.09 to 1.63] P=0.006, respectively). Neopterin levels > or = 12.11 nmol/L at 4 months remained a predictor of death alone and of death or acute coronary events after multivariable adjustment that included adjustment for month 4 low-density lipoprotein cholesterol, high-sensitivity C-reactive protein, and statin regimen (hazard ratio, 2.39 [95% CI, 1.43 to 3.99], P=0.001; and hazard ratio, 1.60 [95% CI, 1.21 to 2.11], P=0.001). High-dose atorvastatin significantly attenuated the risk among subjects with neopterin levels > or = 12.11 nmol/L at baseline (interaction P for death or acute coronary event, 0.018).
Increased monocyte activation detected by an elevated plasma neopterin level identifies patients at long-term risk of death or recurrent acute coronary events after ACS. Intensive statin therapy significantly attenuates the risk of recurrent events among patients with an elevated neopterin level.
单核细胞激活被认为在急性冠状动脉综合征(ACS)的发病机制中起重要作用。蝶呤是单核细胞激活的一种可溶性标志物,其水平升高对稳定型冠状动脉疾病患者具有预后价值。
在普伐他汀或阿托伐他汀评估感染治疗-心肌梗死溶栓(PROVE IT-TIMI 22)试验中,对ACS后平均7天(3946例患者)和4个月(3369例患者)的蝶呤水平进行了测量。我们评估了血浆蝶呤水平与2年内死亡风险以及死亡或急性冠状动脉事件(非致命性心肌梗死或不稳定型心绞痛)风险之间的关系。ACS事件发生7天后,蝶呤水平≥12.11 nmol/L(事后分析得出的上四分位数)与死亡风险增加以及在调整年龄、性别、糖尿病史、高血压史、吸烟史、ACS表现类型、针对索引事件的经皮冠状动脉介入治疗使用情况、他汀类药物治疗方案、低密度脂蛋白胆固醇和高敏C反应蛋白后死亡或急性冠状动脉事件风险增加相关(风险比分别为1.86 [95% CI,1.24至2.77],P = 0.003;以及风险比1.33 [95% CI,1.09至1.63],P = 0.006)。4个月时蝶呤水平≥12.11 nmol/L在多变量调整后(包括调整4个月时的低密度脂蛋白胆固醇、高敏C反应蛋白和他汀类药物治疗方案)仍然是单独死亡以及死亡或急性冠状动脉事件的预测指标(风险比分别为2.39 [95% CI,1.43至3.99],P = 0.001;以及风险比1.60 [95% CI,1.21至2.11],P = 0.001)。高剂量阿托伐他汀显著降低了基线时蝶呤水平≥12.11 nmol/L的受试者中的风险(死亡或急性冠状动脉事件的交互作用P值为0.018)。
血浆蝶呤水平升高检测到的单核细胞激活增加可识别ACS后有长期死亡或复发性急性冠状动脉事件风险的患者。强化他汀类药物治疗显著降低了蝶呤水平升高患者的复发事件风险。