天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2014年
11期
1135-1137
,共3页
马萍%马巧红%刘志军%仇玉民%徐清斌
馬萍%馬巧紅%劉誌軍%仇玉民%徐清斌
마평%마교홍%류지군%구옥민%서청빈
冠心病%氯吡格雷%血管扩张刺激磷蛋白%血小板活化
冠心病%氯吡格雷%血管擴張刺激燐蛋白%血小闆活化
관심병%록필격뢰%혈관확장자격린단백%혈소판활화
coronary disease%clopidogrel%vasodilator-stimulated phosphoprotein%platelet activation
目的:通过检测血管扩张刺激磷蛋白(VASP)磷酸化水平,评价冠心病患者抗血小板聚集治疗前后血小板活性的变化和对氯吡格雷的反应性。方法选取正常对照组28例,不予药物干预;慢性稳定型心绞痛(CSA)95例,将其随机分为A(48例)、B(47例)组,分别给予氯吡格雷75 mg/d、150 mg/d;非ST段抬高型急性冠脉综合征(NST-ACS)67例,首次均给予300 mg负荷量氯吡格雷,此后随机分为C(33例)、D(34例)组,分别序贯给予氯吡格雷75 mg/d、150 mg/d。分别于服用氯吡格雷前、服用负荷剂量氯吡格雷24 h、服用氯吡格雷第5天,取肘静脉血用ELISA法测定血清VASP磷酸化水平。结果服药前,A、B、C、D组血清VASP磷酸化水平均低于正常对照组(P<0.05)。服药后5 d:(1)A、B组血清VASP磷酸化水平较服药前无明显变化(P>0.05);(2)C、D组服用负荷量氯吡格雷24 h及服用维持量第5天血清VASP磷酸化水平均较服药前明显升高(均P<0.05),C、D组服药后两组间血清VASP磷酸化水平变化差异无统计学意义。结论冠心病患者血清VASP磷酸化水平低于正常对照组,氯吡格雷可提高非ST段抬高型急性冠脉综合征患者血清VASP磷酸化水平。
目的:通過檢測血管擴張刺激燐蛋白(VASP)燐痠化水平,評價冠心病患者抗血小闆聚集治療前後血小闆活性的變化和對氯吡格雷的反應性。方法選取正常對照組28例,不予藥物榦預;慢性穩定型心絞痛(CSA)95例,將其隨機分為A(48例)、B(47例)組,分彆給予氯吡格雷75 mg/d、150 mg/d;非ST段抬高型急性冠脈綜閤徵(NST-ACS)67例,首次均給予300 mg負荷量氯吡格雷,此後隨機分為C(33例)、D(34例)組,分彆序貫給予氯吡格雷75 mg/d、150 mg/d。分彆于服用氯吡格雷前、服用負荷劑量氯吡格雷24 h、服用氯吡格雷第5天,取肘靜脈血用ELISA法測定血清VASP燐痠化水平。結果服藥前,A、B、C、D組血清VASP燐痠化水平均低于正常對照組(P<0.05)。服藥後5 d:(1)A、B組血清VASP燐痠化水平較服藥前無明顯變化(P>0.05);(2)C、D組服用負荷量氯吡格雷24 h及服用維持量第5天血清VASP燐痠化水平均較服藥前明顯升高(均P<0.05),C、D組服藥後兩組間血清VASP燐痠化水平變化差異無統計學意義。結論冠心病患者血清VASP燐痠化水平低于正常對照組,氯吡格雷可提高非ST段抬高型急性冠脈綜閤徵患者血清VASP燐痠化水平。
목적:통과검측혈관확장자격린단백(VASP)린산화수평,평개관심병환자항혈소판취집치료전후혈소판활성적변화화대록필격뢰적반응성。방법선취정상대조조28례,불여약물간예;만성은정형심교통(CSA)95례,장기수궤분위A(48례)、B(47례)조,분별급여록필격뢰75 mg/d、150 mg/d;비ST단태고형급성관맥종합정(NST-ACS)67례,수차균급여300 mg부하량록필격뢰,차후수궤분위C(33례)、D(34례)조,분별서관급여록필격뢰75 mg/d、150 mg/d。분별우복용록필격뢰전、복용부하제량록필격뢰24 h、복용록필격뢰제5천,취주정맥혈용ELISA법측정혈청VASP린산화수평。결과복약전,A、B、C、D조혈청VASP린산화수평균저우정상대조조(P<0.05)。복약후5 d:(1)A、B조혈청VASP린산화수평교복약전무명현변화(P>0.05);(2)C、D조복용부하량록필격뢰24 h급복용유지량제5천혈청VASP린산화수평균교복약전명현승고(균P<0.05),C、D조복약후량조간혈청VASP린산화수평변화차이무통계학의의。결론관심병환자혈청VASP린산화수평저우정상대조조,록필격뢰가제고비ST단태고형급성관맥종합정환자혈청VASP린산화수평。
Objective To evaluate the changes of platelet activity before and after anti-platelet treatment in pa?tients with coronary heart disease, and their responsiveness to clopidogrel through detecting the phosphorylation levels of va?sodilator stimulated phosphoprotein (VASP). Methods Twenty-eight cases of healthy people were selected as control group . Patients with chronic stable angina pectoris (CSA, n=95) were randomly divided into A (48 cases) group and B (47 cases) group,and were given clopidogrel 75 mg/d or 150 mg/d respectively;Patients with non ST segment elevation acute coronary syndrome (NST-ACS, n=67) were all given 300 mg loading dose of clopidogrel at the first time, then randomly divid?ed into C (33 cases) group and D (34 cases) group, and given clopidogrel 75 mg/d and 150 mg/d respectively. Blood were tak?en to examine the phosphorylation levels of serum VASP by ELISA before taking clopidogrel, at time point of loading dose and the fifth day of clopidogrel administration . Results Before treatment, phosphorylation levels of serum VASP were low?er in A, B, C, D groups than those in the normal control group(P<0.05). After treatment of clopidogrel for 5 days: ① In group A and group B ,phosphorylation levels of serum VASP did not change compared to that before treatment (P>0.05).②In group C and group D, phosphorylation levels of serum VASP were significantly increased at loading dose and the fifth day of clopidogrel administration than those before treatment (P<0.05), but there were no significant differences in phosphory?lation level of VASP was lower group between group C and group D after serum treatment (P > 0.05). Conclusion The phosphorylation level of serum VASP was lower in patients with coronary heart disease than that in normal control group. Clopidogrel can improve the phosphorylation level of serum VASP in NST-ACS patients .