Moreira Daniel Medeiros, Lueneberg Maria Emilia, da Silva Roberto Leo, Fattah Tammuz, Mascia Gottschall Carlos Antonio
Instituto de Cardiologia de Santa Catarina, São José, and Instituto de Cardiologia do Rio Grande do Sul, Porto Alegre, Brazil.
Cardiology. 2013;126(3):167-70. doi: 10.1159/000351972. Epub 2013 Aug 30.
Methotrexate is a drug that has shown anti-ischemic effects in animal studies and positive results in heart failure clinical trials.
We will randomly assign 80 patients with acute myocardial infarction to receive methotrexate (0.05 mg/kg bolus followed by 0.05 mg/kg/h for 6 h) or matching placebo. The primary outcome will be the area under the curve (AUC) for creatine kinase (CK) release for 72 h. Secondary outcomes will be the peak levels of CK, CK-MB fraction and troponin I, AUC for CK-MB and troponin I, levels of B-type natriuretic peptide (BNP), high-sensitivity C-reactive protein (hsCRP) and erythrocyte sedimentation rate (ESR) at admission and at 30 days, left ventricular ejection fraction (LVEF) at baseline and at 30 days, death, TIMI (thrombolysis in myocardial infarction) frame count in the culprit artery, Killip score after 72 h and rate of reinfarction at 30 days.
We expect a reduction in the AUC for CK, CK-MB and troponin release in the methotrexate group compared to the placebo group. We also expect a reduction in the levels of BNP, hsCRP and ESR and an improvement of LVEF and TIMI frame count in the methotrexate group.
This trial may be the first to demonstrate the anti-inflammatory and anti-ischemic effects of methotrexate in patients with acute myocardial infarction.
甲氨蝶呤是一种在动物研究中显示出抗缺血作用且在心力衰竭临床试验中取得阳性结果的药物。
我们将随机分配80例急性心肌梗死患者接受甲氨蝶呤(0.05mg/kg静脉推注,随后以0.05mg/kg/h持续6小时)或匹配的安慰剂。主要结局将是72小时肌酸激酶(CK)释放的曲线下面积(AUC)。次要结局将是CK、CK-MB同工酶和肌钙蛋白I的峰值水平,CK-MB和肌钙蛋白I的AUC,入院时及30天时B型利钠肽(BNP)、高敏C反应蛋白(hsCRP)和红细胞沉降率(ESR)水平,基线及30天时左心室射血分数(LVEF),死亡情况,罪犯血管的心肌梗死溶栓(TIMI)帧数,72小时后的Killip分级以及30天时的再梗死率。
我们预计与安慰剂组相比,甲氨蝶呤组的CK、CK-MB和肌钙蛋白释放的AUC会降低。我们还预计甲氨蝶呤组的BNP、hsCRP和ESR水平会降低,LVEF和TIMI帧数会改善。
本试验可能是首个证明甲氨蝶呤对急性心肌梗死患者具有抗炎和抗缺血作用的试验。