Bandyopadhyay Dhrubajyoti, Qureshi Arshna, Ghosh Sudeshna, Ashish Kumar, Heise Lyndsey R, Hajra Adrija, Ghosh Raktim K
Department of Internal Medicine, Mount Sinai St Luke's Roosevelt, New York, NY, USA.
Department of Medicine, Lady Hardinge Medical College, New Delhi, India.
J Lipids. 2018 Apr 23;2018:8598054. doi: 10.1155/2018/8598054. eCollection 2018.
The risk of cardiovascular disease has been reported to have a linear relationship with LDL levels. Additionally, the currently recommended LDL target goal of 70 mg/dl does not diminish the CV risk entirely leaving behind some residual risk. Previous attempts to maximally lower the LDL levels with statin monotherapy have met dejection due to the increased side effects associated with the treatment. Nevertheless, with the new advancements in clinical medicine, it has now become possible to bring down the LDL levels to as low as 15 mg/dl using PCSK9 monoclonal antibodies alone or in combination with statins. The development of inclisiran, siRNA silencer targeting PCSK9 gene, is a one step forward in these endeavors. Moreover, various studies aiming to lower the CV risk and mortality by lowering LDL levels have demonstrated encouraging results. The current challenge is to explore this arena to redefine the target LDL levels, if required, to avoid any suboptimal treatment. After thorough literature search in the PubMed, Embase, Scopus, and Google Scholar, we present this article to provide a brief overview of the safety and efficacy of lowering LDL below the current goal.
据报道,心血管疾病风险与低密度脂蛋白(LDL)水平呈线性关系。此外,目前推荐的LDL目标值70mg/dl并不能完全消除心血管风险,仍存在一些残余风险。以往试图通过他汀类单药治疗最大限度降低LDL水平的尝试因治疗相关副作用增加而受挫。然而,随着临床医学的新进展,现在仅使用前蛋白转化酶枯草溶菌素9(PCSK9)单克隆抗体或与他汀类药物联合使用,就有可能将LDL水平降至低至15mg/dl。靶向PCSK9基因的小干扰RNA(siRNA)沉默剂inclisiran的研发是这些努力中的一大进步。此外,旨在通过降低LDL水平降低心血管风险和死亡率的各项研究已取得令人鼓舞的结果。当前的挑战是探索这一领域,必要时重新定义目标LDL水平,以避免任何治疗不充分的情况。在对PubMed、Embase、Scopus和谷歌学术进行全面文献检索后,我们撰写本文以简要概述将LDL降至当前目标值以下的安全性和有效性。