Kim Jin Won, Suh Soon Yong, Choi Cheol Ung, Na Jin Oh, Kim Eung Ju, Rha Seung-Woon, Park Chang Gyu, Seo Hong Seog, Oh Dong Joo
Cardiovascular Center, Korea University, Guro Hospital, 97 Gurodong-Gil, Guro-gu, Seoul, Republic of Korea.
JACC Cardiovasc Interv. 2008 Feb;1(1):65-71. doi: 10.1016/j.jcin.2007.11.002.
This study was designed to investigate whether endothelial dysfunction is related to drug-eluting stent (DES) implantation at 6 months after stenting.
Current available DES could delay vessel healing and subsequently impair endothelial function.
Endothelial function was estimated at 6-month follow-up in 75 patients (31 men, mean age 62.1 years) with a DES (39 sirolimus-eluting stents [SES], 36 paclitaxel-eluting stents [PES]), and 10 patients with a bare-metal stent (BMS) to the left anterior descending artery, by incremental acetylcholine (Ach) infusion (20 microg/min, 50 microg/min, 100 microg/min) and nitrate (200 microg/min) into the left coronary ostium. Vascular responses were quantitatively measured in arterial segments 5 mm proximal and distal to DES and compared with corresponding segments in the BMS group and midsegments in the left circumflex artery as a reference nonstented artery. All antianginal agents were withheld for at least 72 h before coronary angiography.
Greater vasoconstriction to Ach was observed in both the SES and PES groups than in the BMS group or control segments of left circumflex artery. Vasoconstriction to Ach was more prominent in arterial segments distal to stents in both SES and PES groups compared with those in the BMS group (p < 0.001). The degree of vasoconstriction to Ach was similar between the SES and PES groups. Endothelium-independent vasodilatation to nitrate did not differ significantly between the study groups.
Abnormal vasoconstriction to Ach was found in the SES and PES groups, especially in arterial segments distal to DES at 6 months after stenting, which suggests that DES has a potential long-term adverse effect on local coronary endothelial dysfunction.
本研究旨在调查支架植入术后6个月时内皮功能障碍是否与药物洗脱支架(DES)植入有关。
现有的DES可能会延迟血管愈合并随后损害内皮功能。
对75例(31例男性,平均年龄62.1岁)植入DES(39枚西罗莫司洗脱支架[SES],36枚紫杉醇洗脱支架[PES])的患者以及10例植入裸金属支架(BMS)至左前降支的患者,在6个月随访时通过向左冠状动脉口递增注入乙酰胆碱(Ach)(20μg/min、50μg/min、100μg/min)和硝酸盐(200μg/min)来评估内皮功能。在DES近端和远端5mm的动脉节段定量测量血管反应,并与BMS组的相应节段以及作为未植入支架的参考动脉的左旋支动脉中段进行比较。在冠状动脉造影前至少72小时停用所有抗心绞痛药物。
SES组和PES组对Ach的血管收缩均比BMS组或左旋支动脉的对照节段更明显。与BMS组相比,SES组和PES组中支架远端动脉节段对Ach的血管收缩更显著(p<0.001)。SES组和PES组对Ach的血管收缩程度相似。各研究组之间对硝酸盐的非内皮依赖性血管舒张无显著差异。
SES组和PES组中发现对Ach的血管收缩异常,尤其是在支架植入后6个月时DES远端的动脉节段,这表明DES对局部冠状动脉内皮功能障碍有潜在的长期不良影响。