摘要
【目的】氯吡格雷口服对ST段上抬型心肌梗死(STEMI)患者血液中细胞间黏附分子-1(sICAM-1)和P一选择素(P—selectin)水平的影响。【方法】确诊急性sTEMI患者61例,分为常规治疗组(ROU组)31例和氯吡格雷治疗组(CLO组)30例。ROU组接受溶栓(尿激酶)、抗凝(低分子肝素钙)、抗血小板(阿司匹林)、抗心肌重构(卡托普利)及保护心肌(倍他乐克)等药物常规治疗。CLO组除接受前述治疗外,入院时即开始接受氯吡格雷口服治疗(300mg负荷量,继以每日75mg)。比较两组间溶栓治疗后2h内ST段改变、入院后24h内肌酸激酶MB同工酶(CK—MB)浓度变化及入院后48h内血液循环中siCAM-1和P-选择素浓度。【结果】溶栓后2h内ST段降低50%,ROU组为15例(48.4%),CLO组为18例(60.0%),两组间无显著性差异(P〉0.05)。两组CK—MB浓度,在入院后即刻、入院后4h差异无显著性(P〉0.05),而在入院后8h、入院后12h、入院后24hCLO组显著低于ROU组(P〈0.05,P〈0.01)。入院后48hICAM-1浓度及P-选择素浓度CLO组显著低于ROU组(P〈0.05,P〈0.01)。【结论】对于STEMI患者,在常规治疗外早期联用氯吡格雷治疗,可限制心肌梗死范围,并可降低血液中siCAM-1和P-选择素浓度。
[Objective] To evaluate the effect of clopidogrel therapy on intercellular adhesion molecule-1 (ICAM-1) and P-selectin in patients with ST-segment elevated myocardial infarction(STEMI). [Methods] Sixty-one STEMI patients were enrolled and divided randomly into two groups. One was the routine pharmacological reperfusion therapy group (ROU group, n = 31), who received 300mg aspirin, 10000IU low-weight molecular heparin and urokinase therapy. Clopidogrel with 300mg loading and 75mg/d thereafter was added to standard reperfusion therapy in the other group (CLO group, n = 30). The ST-segment resolution and CK-MB were measured. The plasma levels of soluble ICAM-1 and P-selectin 48h at admission were assayed by ELISA method. [Results]At 2h after thrombolysis, ST-segment reduced at 50% in 15 patients (48.4%) in ROU group and 18 patients (60.0%) in CLO group, and there was no significant difference between two groups( P 〉0.05). At once at admission and after 4h, there was no significant difference in CK-MB level between two groups. At 8h, 12h and 24h after administration, CK-MB level in ROU group was significantly higher than that in CLO group( P 〈0.05, P 〈0.01). At 48h at admission, ICAM-1 and P-selectin levels in CLO group were significantly lower than those in ROU group( P 〈0.05, P 〈0.01). [Conclusion]Routine treatment com bined with clopidogrel for treating STEMI patients can limit myocardial infarction area and decrease ICAM-1 and P-selectin concentration.
出处
《医学临床研究》
CAS
2010年第3期472-474,共3页
Journal of Clinical Research