Li Runjun, Tang Xiuying, Jing Quanmin, Wang Qingsheng, Yang Meihong, Han Xiaoyu, Zhao Jiayu, Yu Xiangyou
Department of Critical Care Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China; Department of Emergency Medicine, The First Hospital of QinHuangDao, QinHuangDao, HeBei, China.
Department of Cardiology, The First Hospital of QinHuangDao, QinHuangDao, HeBei, China.
Am J Emerg Med. 2017 Nov;35(11):1657-1661. doi: 10.1016/j.ajem.2017.05.024. Epub 2017 May 23.
Trimetazidine (TMZ) improves clinical outcomes in patients with chronic heart failure and stable coronary artery disease. No study has yet evaluated the efficacy of TMZ in type 2 diabetes patients with acute myocardial infarction (AMI) undergoing Percutaneous Coronary Intervention (PCI). We performed this study to evaluate the efficacy TMZ in DM patients with AMI undergoing PCI, such as the effect on reductions in myocardial enzyme, improvements in liver function, modulation of glucose levels, and improvement in cardiac function.
For this randomized study, we enrolled 173 AMI patients with type 2 diabetes undergoing PCI between January 1, 2014, and January 1, 2016. All patients received aspirin and ticagrelor upon admission and throughout their hospitalization. Patients in the experimental group were treated with a loading dose of 60mg TMZ at admission, and 20 mg TMZ three times a day thereafter. 89 patients were included in experimental group, and 84 patients were included in control group. All patients received PCI treatments. The endpoints evaluated were serum creatine kinase and its isoenzyme (CK and CK-MB), cardiac troponin I (cTNI), serum creatinine (Cr), serum urea, blood glucose, serum glutamic pyruvic transaminase (ALT), serum glutamic oxaloacetictransaminase (AST), left atrial dimension (LA), left ventricular ejection fraction (LVEF), left ventricular end-diastolic dimension (LVEDD), and cardiac output (CO).
Compared with the control group, TMZ treatment significantly reduced CK and CK-MB on the second day in hospital ([797±582] vs. [1092±1114]; [80±60] vs. [105±100]; p=0.029, p=0.041, respectively), and cTNI after one and six days in hospital ([13.5±12.7] vs. [19.8±19.2]; [3.3±3.2] vs. [4.8±4.7]; two-tailed p=0.012). In addition, TMZ significantly lowered liver enzymes (ALT, AST) at 6days ([29.0±11.6] vs. [42.4±24.5]; [39.8±17.3] vs. [69.2±70.0]; two-tailed p=0.000), lowered glucose after 6days ([6.80±2.12] vs. [7.59±2.24]; p=0.019), and increased LVEF after ten to fourteen days ([58.4±8.6] vs. [54.9±8.4]; p=0.008). There were no significant effect on Cr and serum urea (p=0.988, p=0.569, respectively), nor on LA, LVEDD, and CO ([36.3±4.5] vs. [37.0±4.1], p=0.264; [52.0±4.9] vs. [53.1±4.6], p=0.128; [5.4±0.9] vs. [5.4±0.9], p=0.929, respectively).
Among type 2 diabetic patients with AMI undergoing PCI, TMZ significantly reduces serum myocardial enzyme, improves liver function, adjusts blood glucose and improves cardiac function.
曲美他嗪(TMZ)可改善慢性心力衰竭和稳定型冠状动脉疾病患者的临床预后。尚无研究评估TMZ对接受经皮冠状动脉介入治疗(PCI)的2型糖尿病急性心肌梗死(AMI)患者的疗效。我们开展本研究以评估TMZ对接受PCI的AMI糖尿病患者的疗效,如对心肌酶降低、肝功能改善、血糖调节及心功能改善的影响。
在本随机研究中,我们纳入了2014年1月1日至2016年1月1日期间173例接受PCI的2型糖尿病AMI患者。所有患者入院时及住院期间均接受阿司匹林和替格瑞洛治疗。实验组患者入院时给予60mg TMZ负荷剂量,此后每日3次,每次20mg TMZ。实验组纳入89例患者,对照组纳入84例患者。所有患者均接受PCI治疗。评估的终点指标包括血清肌酸激酶及其同工酶(CK和CK-MB)、心肌肌钙蛋白I(cTNI)、血清肌酐(Cr)、血清尿素、血糖、血清谷丙转氨酶(ALT)、血清谷草转氨酶(AST)、左房内径(LA)、左室射血分数(LVEF)、左室舒张末期内径(LVEDD)和心输出量(CO)。
与对照组相比,TMZ治疗显著降低了住院第2天的CK和CK-MB(分别为[797±582] vs. [1092±1114];[80±60] vs. [105±100];p=0.029,p=0.041),以及住院1天和6天后的cTNI(分别为[13.5±12.7] vs. [19.8±19.2];[3.3±3.2] vs. [4.8±4.7];双侧p=0.012)。此外,TMZ在第6天时显著降低了肝酶(ALT、AST)(分别为[29.0±11.6] vs. [42.4±24.5];[39.8±17.3] vs. [69.2±70.0];双侧p=0.000),在第6天后降低了血糖([6.80±2.12] vs. [7.59±2.24];p=0.019),并在10至14天后提高了LVEF([58.4±8.6] vs. [54.9±8.4];p=0.008)。对Cr和血清尿素无显著影响(分别为p=0.988,p=0.569),对LA、LVEDD和CO也无显著影响(分别为[36.3±4.5] vs. [37.0±4.1],p=0.264;[52.0±4.9] vs. [53.1±4.6],p=0.128;[5.4±0.9] vs. [5.4±0.9],p=0.929)。
在接受PCI的2型糖尿病AMI患者中,TMZ可显著降低血清心肌酶,改善肝功能,调节血糖并改善心功能。