首页> 美国卫生研究院文献>Indian Heart Journal >Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors in aortic stenosis - Is this the light at the end of the tunnel for patients with aortic stenosis?
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Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors in aortic stenosis - Is this the light at the end of the tunnel for patients with aortic stenosis?

机译:Proprotein转化酶枯草杆菌蛋白酶/ kexin型9(PCSK9)主动脉狭窄中的抑制剂 - 这是主动脉狭窄患者隧道末端的光吗?

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摘要

The exploratory analysis of FOURIER trial has offered a ray of hope for patients with nonrheumatic aortic stenosis (AS). At present, the only definitive treatment of severe AS is aortic valve replacement (AVR). Despite transaortic valvular replacement revolutionizing the treatment of AS, it still remains a progressive condition, with no disease-modifying pharmacotherapy. Angiotensin-converting-enzyme inhibitors, angiotensin receptor blockers, eplerenone, nitrates and statins all have been tried previously but failed to slow down the progression of aortic stenosis. Recently, there has been an emerging role of lipoprotein A [Lp(a)] in the pathogenesis of AS. This raises the possibility that long-term therapy with specific emphasis on Lp(a) reduction may reduce or slow the progression of AS.
机译:对傅立叶试验的探索性分析为非空心主动脉狭窄(AS)的患者提供了一种希望。目前,唯一的定期治疗严重的是主动脉瓣置换(AVR)。尽管纵向瓣膜置换革命性地彻底改变了治疗,但它仍然仍然是进步的病情,没有疾病改性药物疗法。血管紧张素转化酶抑制剂,血管紧张素受体阻滞剂,ePLER烯酮,硝酸盐和毒素都已尝试以前但未能减缓主动脉狭窄的进展。最近,脂蛋白A [LP(a)]在载体的发病机制中存在新兴作用。这提出了具有对LP(a)减少的特异性强调的长期治疗可能会降低或减缓as的进展。

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