目的 探讨ST段抬高型心肌梗死(ST-Segment elevation myocardial infarction, STEMI)患者急诊经皮冠状动脉介入术(percutaneous coronary intervention, PCI)前给予80 mg阿托伐他汀强化治疗对术后心肌血流灌注及血清sCD40L的影响。方法 对拟行急诊PCI的STEMI(<12 h)患者,随机分为A、B、C 3组。A组术前阿托伐他汀80 mg,术后40 mg/晚,1个月后改为 20 mg/晚;B组术前未给予阿托伐他汀,术后40 mg/晚,1个月后改为20 mg/晚;C组术前未给予阿托伐他汀,术后20 mg/晚。观察术后即刻TIMI血流分级、校正TIMI血流帧数(corrected TIMI frame count,cTFC)以及各组术前、术后24 h、术后7 d及术后30 d血清sCD40L的水平变化;同时记录用药期间的药物不良反应。结果 术后cTFC比较,A组(25.44±12.07)显著小于B组(30.98±12.09)、C组(33.49±14.56),差异有统计学意义(P<0.05);而3组间TIMI3级血流比例依次为91.7%(44/48)、88.4%(38/43)、86.7%(39/45),组间比较,差异无统计学意义。急诊PCI术后24 h及7 d,A组血清sCD40L水平[(16.18±4.52)ng/ml,(3.92±1.44)ng/ml]低于B组[(18.25±5.02)ng/ml,(4.63±1.68)ng/ml]及C组[(18.66±4.17)ng/ml,(4.68±1.51)ng/ml],差异有统计学意义(P<0.05);术后30 d 3组间比较无统计学差异。3组用药期间无严重药物不良反应发生。结论 STEMI患者急诊PCI术前给予负荷剂量阿托伐他汀治疗可显著改善术后心肌血流灌注及炎性反应程度,且安全性好。
Abstract
Objective To study the effects of a loading-dose atorvastatin on the coronary blood pefusion and serum sCD40L after primary PCI in STEMI patients. Methods STEMI patients who were prepared for primary PCI were randomly divided into three groups: group A (received atorvastatin 80 mg loading dose before PCI then followed by 40 mg daily for one month and a maintenance dose of 20 mg daily thereafter), group B (received atorvastatin 40 mg daily after PCI for one month and a maintenance dose of 20 mg daily thereafter) and group C (received atorvastatin 20 mg daily after PCI). TIMI flow grade and corrected TIMI frame count (cTFC) after PCI were recorded and compared between the three groups. In addition, the serum sCD40L was measured at admission and 24 h, 7 d, 30 d after PCI. Adverse reactions were monitored during 30 d follow-up. Results The cTFC in group A (25.44±12.07) was significamtly lower than that in group B (30.98±12.09) or that in group C (33.49±14.56) (P<0.05); The percentages of TIMI grade 3 were 91.7% (44/48),88.4% (38/43),86.7% (39/45) in group A, group B and group C respectively, and no significant difference was found among the three groups. The levels of serum sCD40L at 24 h and 7 d after PCI in group A [(16.18±4.52) ng/ml, (3.92±1.44) ng/ml]were significantly lower than those in group B [(18.25±5.02) ng/ml, (4.63±1.68) ng/ml] and group C [(18.66±4.17) ng/ml,(4.68±1.51) ng/ml]. But the levels of sCD40L in the three groups did not reach statistical differences at 30 d after PCI. No severe adverse reactions were observed during study period. Conclusions For STEMI patients who undergo primary PCI, a loading-dose of atorvastatin before PCI can reduce serum sCD40L level, improve immediate coronary blood perfusion and does not increase the incidences of adverse events.
关键词
急性ST段抬高型心肌梗死 /
阿托伐他汀 /
sCD40L /
校正TIMI血流帧数 /
他汀安全性
Key words
ST segment elevated myocardial infarction /
atorvastatin /
sCD40L /
corrected TIMI frame count /
statin safety
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] Kiernan T J, Ruggiero N N, Bernal J M, et al. The no-reflow phenomenon in the coronary circulation [J]. Cardiovasc Hematol Agents Med Chem, 2009, 7(3):181-192.
[2] Brosh D, Assali A R, Mager A, et al. Effect of no-reflow during primary percutaneous coronary intervention for acute myocardial infarction on six-month mortality [J]. Am J Cardiol, 2007, 99(4):442-445.
[3] O’Donoghue M L, Bhatt D L, Flather M D,et al. Atopaxar and its effects on markers of platelet activation and inflammation: results from the LANCELOT CAD program[J].J Thromb Thrombolysis,2012,34(1):36-43.
[4] Davi G, Tuttolomondo A, Santilli F, et al. CD40 ligand and MCP-1 as predictors of cardiovascular events in diabetic patients with stroke [J]. J Atheroscler Thromb,2009,16(6):707-713.
[5] Dominguez-Rodriguez A, Abreu-Gonzalez P, Garcia-Gonzalez M J, et al. Soluble CD40 ligand: interleukin-10 ratio predicts in-hospital adverse events in patients with ST-segment elevation myocardial infarction [J]. Thromb Res,2007,121(3):293-299.
[6] Liu H L, Yang Y, Yang S L, et al. Administration of a loading dose of atorvastatin before percutaneous coronary intervention prevents inflammation and reduces myocardial injury in STEMI patients: a randomized clinical study [J]. Clin Ther,2013,35(3): 261-272.
[7] Gibson C M, Cannn C P, Daley W L, et al. TIMI frame count: a quantitative method of assessing coronary artery flow [J]. Circulation,1996,93(5):879-888.
[8] Yan J, Wu Z, Huang Z, et al. Clinical implications of increased expression of CD40L in patients with acute coronary syndromes [J]. Chin Med J,2002,115(4):491-493.
[9] 苑雯雯,杨 勇,赵旭燕, 等. 急诊经皮冠状动脉介入治疗前强化阿托伐他汀对急性心肌梗死患者的中期疗效观察[J]. 中华老年心脑血管病杂志, 2012, 14(9): 903-906.
[10] Kim J S, Kim J, Choi D, et al. Efficacy of high-dose atorvastatin loading before primary percutaneous coronary intervention in ST-segment elevation myocardial infarction: the STATIN STEMI trial[J]. JACC Cardiovasc Interv,2010,3(3):332-339.
[11] 郑 博, 王新刚, 龚艳君,等. 直接经皮冠状动脉介入治疗术前负荷剂量阿托伐他汀治疗对急性心肌梗死患者近期预后的影响[J]. 中国介入心脏病学杂志,2013,21(1): 41-45.
[12] Hahn J Y, Kim H J, Choi Y J, et al. Effects of atorvastatin pretreatment on infarct size in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention [J]. Am Heart J, 2011, 162(6):1026-1033.
[13] Krotz F, Schiele T M, Zahler S, et al. Sustained platelet activation following intracoronary beta irradiation [J]. Am J Cardiol,2002,90(12):1381-1384.
[14] Hassan G S, Merhi Y, Mourad W. CD40 Ligand: a neo-inflammatory molecule in vascular diseases [J]. Immunobiology,2012,217(5): 521-532.
[15] Blanco-Colio L M, Martín-Ventura J L, De Teresa E, et al. Atorvastatin decreases elevated soluble CD40L in subjects at high cardiovascular risk. Atorvastatin on inflammatory markers study: a substudy of ACTFAST [J]. Kidney Int Suppl,2008,74(Suppl 111): S60-S63.
[16] Durakocgˇ lugi M E, Kocaman S A, Cetin M, et al. Increased circulating soluble CD40 levels in patients with slow coronary flow phenomenon: an observational study [J]. Anadolu Kardiyol Derg,2013,13(1): 39-44.