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铁螯合对 ST 段抬高型心肌梗死心肌梗死面积和氧化应激的影响。

Effect of iron chelation on myocardial infarct size and oxidative stress in ST-elevation-myocardial infarction.

机构信息

Department of Cardiovascular Medicine, Alfred Hospital, Melbourne, Australia.

出版信息

Circ Cardiovasc Interv. 2012 Apr;5(2):270-8. doi: 10.1161/CIRCINTERVENTIONS.111.966226. Epub 2012 Apr 10.

Abstract

BACKGROUND

Experimental studies suggest that deferoxamine (DFO) limits the generation of reactive oxygen species by chelating redox-active iron and thereby may reduce ischemia-reperfusion injury and myocardial infarct (MI) size. We investigated whether DFO administered before reperfusion by primary percutaneous coronary intervention (PPCI) would ameliorate oxidative stress and MI size.

METHODS AND RESULTS

We randomly assigned 60 patients with ST-elevation-MI to receive an intravenous bolus of DFO (500 mg) immediately before PPCI followed by a 12-hour infusion (50 mg/kg of body weight) (n=28) or normal saline bolus and infusion (placebo group, n=32). MI size was measured by contrast-enhanced cardiac MRI (CMRI; day 3±1), creatine kinase and troponin I area-under-the-curve, and severity of wall motion abnormality on echocardiography. Clinical follow-up including repeat CMRI and echocardiography were performed at 3 months (100±17 days). Oxidative stress was assessed by plasma F(2)-isoprostane levels. DFO and placebo groups were well balanced with respect to baseline characteristics, symptom- and door-to-balloon times, pre-PPCI coronary patency, and infarct-related artery location. Serum iron levels were decreased with DFO treatment after PPCI compared with placebo (3.0±2.5 versus 12.6±5.5 μmol/L, P<0.0001), which persisted until the end of the infusion. In DFO-treated patients, there was a significant reduction in plasma F(2)-isoprostane levels immediately after PPCI (2878±1461 versus 2213±579 pmol/L, P=0.04). However, there was no difference in CMRI-determined infarct size (DFO, 17.4±10.8%, versus placebo, 18.6±10.2%; P=0.73), myocardial salvage index at 3 days or at 3 months, or the area-under-the-curve for creatine kinase or troponin I.

CONCLUSIONS

Adjunctive DFO treatment after the onset of ischemia and continued periprocedurally ameliorates oxidative stress without limiting infarct size.

CLINICAL TRIAL REGISTRATION

URL: http://www.anzctr.org.au/. Unique identifier: ACTRN12608000308392.

摘要

背景

实验研究表明,去铁胺(DFO)通过螯合氧化还原活性铁来限制活性氧的产生,从而可能减轻缺血再灌注损伤和心肌梗死(MI)的面积。我们研究了通过经皮冠状动脉介入治疗(PPCI)再灌注前给予 DFO 是否会改善氧化应激和 MI 面积。

方法和结果

我们将 60 名 ST 段抬高型心肌梗死患者随机分为两组:立即在 PPCI 前给予 DFO(500mg)静脉推注,然后进行 12 小时输注(50mg/kg 体重)(n=28)或生理盐水推注和输注(安慰剂组,n=32)。通过对比增强心脏 MRI(CMRI;第 3 天±1 天)、肌酸激酶和肌钙蛋白 I 曲线下面积以及超声心动图上的壁运动异常严重程度来测量 MI 面积。在 3 个月(100±17 天)时进行临床随访,包括重复 CMRI 和超声心动图。氧化应激通过血浆 F(2)-异前列腺素水平来评估。DFO 和安慰剂组在基线特征、症状和门球时间、PPCI 前的冠状动脉通畅性和梗死相关动脉位置方面无差异。与安慰剂组相比,DFO 治疗后 PPCI 后血清铁水平降低(3.0±2.5 与 12.6±5.5 μmol/L,P<0.0001),并且持续到输注结束。在 DFO 治疗的患者中,PPCI 后血浆 F(2)-异前列腺素水平显著降低(2878±1461 与 2213±579 pmol/L,P=0.04)。然而,CMRI 确定的梗死面积(DFO,17.4±10.8%,与安慰剂,18.6±10.2%;P=0.73)、3 天时或 3 个月时的心肌挽救指数、肌酸激酶或肌钙蛋白 I 的曲线下面积均无差异。

结论

缺血发作后辅助 DFO 治疗并持续进行可改善氧化应激而不限制梗死面积。

临床试验注册

网址:http://www.anzctr.org.au/。独特标识符:ACTRN12608000308392。

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