Kelly Dominic, Squire Iain B, Khan Sohail Q, Quinn Paulene, Struck Joachim, Morgenthaler Nils G, Davies Joan E, Ng Leong L
Department of Cardiovascular Sciences, University of Leicester, UK.
J Card Fail. 2008 Nov;14(9):739-45. doi: 10.1016/j.cardfail.2008.07.231. Epub 2008 Aug 30.
Acute myocardial infarction (AMI) is associated with left ventricular (LV) dysfunction and clinical heart failure. Arginine vasopressin is elevated in heart failure and the C-terminal of provasopressin (Copeptin) is associated with adverse outcome post-AMI. The aim of this study was to describe the association between Copeptin with LV dysfunction, volumes, and remodeling and clinical heart failure post-AMI.
We studied 274 subjects with AMI. Copeptin was measured from plasma at discharge and subjects underwent echocardiography at discharge and follow-up (median 155 days). Subjects were followed for clinical heart failure for a median of 381 days. Remodeling was assessed as the change (Delta) in LV volumes between echo examinations. Copeptin correlated directly with wall motion index score (WMIS) and inversely with LV ejection fraction (LVEF) at discharge (WMIS, r=0.276, P < .001; LVEF, r=-0.188, P=.03) and follow-up (WMIS, r=0.244, P < .001; LVEF, r=-0.270, P < .001) and with ventricular volumes at follow-up (LVEDV, r=0.215, P=.002; LVESV, r=0.299, P < .001). Copeptin was associated with ventricular remodeling; DeltaEDV; r=0.171, P=0.015, DeltaESV; r=0.186, P=.008. Subjects with increasing LVESV had higher levels of Copeptin (median 6.30 vs. 5.75 pmol/L, P=.012). Subjects with clinical heart failure (n=30) during follow-up had higher Copeptin before discharge (median 13.55 vs. 5.80, P < .001). In a Cox proportional hazards model, Copeptin retained association with clinical heart failure. Kaplan-Meier assessment revealed increased risk in subjects with Copeptin >6.31 pmol/L.
Copeptin is associated with LV dysfunction, volumes, and remodeling and clinical heart failure post-AMI. Measurement of Copeptin may provide prognostic information and the AVP system may be a therapeutic target in post-MI LV dysfunction.
急性心肌梗死(AMI)与左心室(LV)功能障碍及临床心力衰竭相关。心力衰竭时精氨酸加压素水平升高,而前加压素的C末端( copeptin )与AMI后的不良预后相关。本研究旨在描述copeptin与AMI后左心室功能障碍、容积、重构及临床心力衰竭之间的关联。
我们研究了274例AMI患者。出院时测定血浆copeptin水平,并在出院时及随访(中位时间155天)时对患者进行超声心动图检查。对患者随访临床心力衰竭情况,中位随访时间为381天。重构通过两次超声心动图检查之间左心室容积的变化(Delta)来评估。出院时及随访时,copeptin与室壁运动指数评分(WMIS)呈正相关,与左心室射血分数(LVEF)呈负相关(出院时WMIS,r = 0.276,P <.001;LVEF,r = -0.188,P =.03;随访时WMIS,r = 0.244,P <.001;LVEF,r = -0.270,P <.001),且与随访时的心室容积相关(左心室舒张末期容积,r = 0.215,P =.002;左心室收缩末期容积,r = 0.299,P <.001)。Copeptin与心室重构相关;DeltaEDV,r = 0.171,P = 0.015,DeltaESV,r = 0.186,P =.008。左心室收缩末期容积增加的患者copeptin水平较高(中位值6.30对5.75 pmol/L,P =.012)。随访期间发生临床心力衰竭的患者(n = 30)出院前copeptin水平较高(中位值13.55对5.80,P <.001)。在Cox比例风险模型中,copeptin与临床心力衰竭仍有关联。Kaplan-Meier评估显示,copeptin>6.31 pmol/L的患者风险增加。
Copeptin与AMI后左心室功能障碍、容积、重构及临床心力衰竭相关。测定copeptin可能提供预后信息,且血管加压素系统可能是心肌梗死后左心室功能障碍的治疗靶点。