Romano Alfredo, Jensen Michael Rugaard, McAlpine Jim
Celgene International Sàrl, Route de Perreux 1, 2017 Boudry, Switzerland.
Curr Opin Drug Discov Devel. 2010 Mar;13(2):157-8.
Coronary artery disease consists of obstruction (stenosis) of the coronary arteries by the deposition of atherosclerotic plaques, resulting in an insufficient supply of oxygen to the heart muscle. Treatment options include the insertion of a stent - a metal mesh tube - into the obstructed vessel to keep the artery open, thus preventing acute occlusion and restenosis. The occlusion of vessels resulting from subacute stent thrombosis and late in-stent restenosis are potential complications after successful revascularization. However, the rate of stent thrombosis has been reduced dramatically by means of adequate antiplatelet therapy, and in-stent restenosis has been addressed successfully with drug-eluting stents. These drug-eluting stents are engineered to release bioactive agents into the affected blood vessels, plaques or tissues adjacent to the stent. Various antimitotic, anti-inflammatory, and anticoagulant immunosuppressive agents have been attached to stents, including sirolimus and tacrolimus. Future opportunities include the use of gene therapies released from gene-eluting stents. These advances highlight some of the opportunities for optimizing stent-based treatment for coronary artery disease.
冠状动脉疾病是指冠状动脉因动脉粥样硬化斑块沉积而发生阻塞(狭窄),导致心肌供氧不足。治疗选择包括在阻塞血管中植入支架(一种金属网管)以保持动脉通畅,从而预防急性闭塞和再狭窄。亚急性支架血栓形成和晚期支架内再狭窄导致的血管闭塞是成功血管重建术后的潜在并发症。然而,通过充分的抗血小板治疗,支架血栓形成的发生率已大幅降低,药物洗脱支架也已成功解决了支架内再狭窄问题。这些药物洗脱支架被设计成可将生物活性剂释放到受影响的血管、斑块或支架附近的组织中。各种抗有丝分裂、抗炎和抗凝免疫抑制剂已被附着在支架上,包括西罗莫司和他克莫司。未来的机遇包括使用从基因洗脱支架释放的基因疗法。这些进展凸显了一些优化基于支架的冠状动脉疾病治疗的机遇。