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[非甾体抗炎药与心血管疾病风险]

[Nonsteroidal anti-inflammatory drugs and the risk of cardiovascular diseases].

作者信息

Jukić Anita, Kaliterna Dusanka Martinović, Radić Mislav

机构信息

Zavod za kardiovaskularne bolesti, Klinika za unutarnje bolesti Klinicki bolnicki centar Split, Soltanska 1, 21000 Split.

出版信息

Reumatizam. 2010;57(1):26-8.

Abstract

Non-steroidal anti-inflammatory drugs act as nonselective inhibitors of the enzyme cyclooxygenase (catalyzes the formation ofprostaglandins), inhibiting both the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) isoenzymes. Selective COX-2 inhibitors have reduced gastrointestinal related adverse events but increased the risk of cardiovascular diseases. Selective COX-2 inhibitors may tip the natural balance between prothrombotic thromboxane A2 and antithrombotic prostacyclin potentially increasing the possibility of a thrombotic cardiovascular event. Decreased prostacycline synthesis, a vasodilatator and modulator of platelet activation, contributing to platelet aggregation and vasoconstriction. Some studies have suggested that NSAID increase the risk of cardiovascular events and for patients at high cardiovascular risk we should use them with great caution.

摘要

非甾体抗炎药作为酶环氧化酶(催化前列腺素的形成)的非选择性抑制剂,抑制环氧化酶-1(COX-1)和环氧化酶-2(COX-2)两种同工酶。选择性COX-2抑制剂减少了胃肠道相关不良事件,但增加了心血管疾病的风险。选择性COX-2抑制剂可能会打破促血栓形成的血栓素A2和抗血栓形成的前列环素之间的自然平衡,从而潜在地增加血栓性心血管事件的可能性。前列环素合成减少,前列环素是一种血管舒张剂和血小板活化调节剂,会导致血小板聚集和血管收缩。一些研究表明,非甾体抗炎药会增加心血管事件的风险,对于心血管风险高的患者,我们应谨慎使用。

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