PAS三联疗法对急性脑梗死患者血脂、血清sCD40L及MMP-9水平及颈动脉易损斑块稳定性的影响

被引:9
作者
李强
凌芳
肖家平
唐智敏
黄天志
机构
[1] 武汉市第五医院神经内科
关键词
脑梗死; 阿托伐他汀; 普罗布考; 可溶性CD40配体; 基质金属蛋白酶-9; 动脉粥样硬化;
D O I
10.19845/j.cnki.zfysjjbzz.2011.12.009
中图分类号
R743.3 [急性脑血管疾病(中风)];
学科分类号
1002 ;
摘要
目的探讨普罗布考、阿司匹林、他汀类药物(PAS)三联疗法对急性脑梗死患者血脂、血清超敏C-反应蛋白(hs-CRP)、可溶性CD40配体(sCD40L)及基质金属蛋白酶-9(MMP-9)水平的影响,观察其对颈动脉易损斑块稳定性的影响。方法根据颈动脉超声检查结果分为颈动脉稳定斑块组(n=45)和颈动脉易损斑块组(n=90)。将稳定斑块组作为对照组,按随机数字法将易损斑块组分为AS组(n=45,阿司匹林100mg/d,阿托伐他汀20mg/d,口服)和PAS组(n=45,AS基础上加用普罗布考片,0.25/次,2次/日,口服)。比较治疗前后血脂、血清hs-CRP、sCD40L和MMP-9水平;观察治疗前后颈动脉内-中膜厚度(IMT值)、斑块Crous积分及斑块回声变化。结果治疗后4w,两组中TG、TC、LDL-C、血清hs-CRP、sCD40L和MMP-9水平均下降,PAS组中各项指标下降幅度均大于AS组,差异具有显著性(P均<0.01);治疗后12个月,两组IMT值和斑块Crous积分较治疗前减少,且PAS组两项指标低于AS组,PAS组低回声斑块回声增强例数高于AS组(P均<0.01)。结论 PAS三联疗法是一种安全有效的治疗方法,具有更强的降脂抗炎作用,可逆转和稳定斑块。
引用
收藏
页码:1090 / 1093
页数:4
相关论文
共 6 条
[1]   Oxidized LDL in human carotid plaques is related to symptomatic carotid disease and lesion instability [J].
Sigala, Fragiska ;
Kotsinas, Athanassios ;
Savari, Paraskevi ;
Filis, Konstantinos ;
Markantonis, Sophia ;
Iliodromitis, Efstathios K. ;
Gorgoulis, Vassilis G. ;
Andreadou, Ioanna .
JOURNAL OF VASCULAR SURGERY, 2010, 52 (03) :704-713
[2]  
Pre-ischemic exercise reduces matrix metalloproteinase-9 expression and ameliorates blood–brain barrier dysfunction in stroke[J] . M. Guo,B. Cox,S. Mahale,W. Davis,A. Carranza,K. Hayes,S. Sprague,D. Jimenez,Y. Ding.Neuroscience . 2008 (2)
[3]   CD40/CD40 ligand signaling in mouse cerebral microvasculature after focal ischemia/reperfusion [J].
Ishikawa, M ;
Vowinkel, T ;
Stokes, KY ;
Arumugam, TV ;
Yilmaz, G ;
Nanda, A ;
Granger, DN .
CIRCULATION, 2005, 111 (13) :1690-1696
[4]  
Different expression of MMPs/TIMP-1 in human atherosclerotic lesions. Relation to plaque features and vascular bed[J] . Atherosclerosis . 2003 (2)
[5]   Increased levels of markers of vascular inflammation in patients with coronary heart disease [J].
Schumacher, A ;
Seljeflot, I ;
Sommervoll, L ;
Christensen, B ;
Otterstad, JE ;
Arnesen, H .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 2002, 62 (01) :59-68
[6]  
Anti-inflammatory and im-mune modulation therapy against atherosclerosis. Yamashita T,Hirata K. Japanese Journal of Clinical Medicine . 2011