New approaches in the pharmacotherapy of dyslipidemia and atherosclerosis

M. Maksimov, K. O. Shnaider, A. A. Zvegintseva
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Abstract

Cardiovascular diseases are the leading cause of death worldwide. Dyslipidemia is one of the most significant modifiable risk factors for the CVD development and potentiation. The main drugs in the treatment of dyslipidemia in modern clinical practice are statins, although there are other effective hypolipidemic drugs that are gaining popularity, such as ezetimibe, proprotein convertase subtilisin/kexin type inhibitors - PCSK9 inhibitors, antisense oligonucleotide (pelacarsen), small interfering RNA - siRNA (inclisiran), and some others. In real clinical practice, the most effective approach to achieve LDL-C targets is adding ezetimibe to a statin (simvastatin, atorvastatin, rosuvastatin, etc.), rather than titrating the statin dose to the maximum possible. The addition of siRNA to statin therapy resulted in a stable, significant reduction in LDL levels by an average of 50% in all groups compared with statin monotherapy.
血脂异常和动脉粥样硬化药物治疗的新途径
心血管疾病是世界范围内导致死亡的主要原因。血脂异常是心血管疾病发生和加重最重要的可改变危险因素之一。现代临床治疗血脂异常的主要药物是他汀类药物,但也有其他有效的降血脂药物越来越受欢迎,如依折替米、蛋白转化酶subtilisin/ keexin型抑制剂- PCSK9抑制剂、反义寡核苷酸(pelacarsen)、小干扰RNA - siRNA (inclisiran)等。在实际临床实践中,达到LDL-C目标最有效的方法是在他汀类药物(辛伐他汀、阿托伐他汀、瑞舒伐他汀等)中加入依泽替米贝,而不是将他汀类药物的剂量调至最大。与他汀类药物单药治疗相比,在他汀类药物治疗中加入siRNA可使LDL水平稳定显著降低50%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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