Texas Tech University Health Sciences Center, El Paso, Texas, USA.
Independent Researcher.
Curr Opin Cardiol. 2024 Jul 1;39(4):292-299. doi: 10.1097/HCO.0000000000001144. Epub 2024 Mar 26.
RNA interference (RNAi)-based therapies that target specific gene products have impacted clinical medicine with 16 FDA approved drugs. RNAi therapy focused on reducing plasma lipoprotein(a) [Lp(a)] levels are under evaluation.
RNAi-based therapies have made significant progress over the past 2 decades and currently consist of antisense oligonucleotides (ASO) and small interfering RNA (siRNA). Chemical modification of the RNA backbone and conjugation of siRNA enables efficient gene silencing in hepatocytes allowing development of effective cholesterol lowering therapies. Multiple lines of evidence suggest a causative role for Lp(a) in atherosclerotic cardiovascular disease, and recent analyses indicate that Lp(a) is more atherogenic than low density lipoprotein- cholesterol (LDL-C). These findings have led to the 'Lp(a) hypothesis' that lowering Lp(a) may significantly improve cardiovascular outcomes. Four RNAi-based drugs have completed early phase clinical trials demonstrating >80% reduction in plasma Lp(a) levels. Phase 3 clinical trials examining clinical outcomes with these agents are currently underway.
Currently, four RNAi-based drugs have been shown to be effective in significantly lowering plasma Lp(a) levels. Clinical outcome data from phase 3 trials will evaluate the Lp(a) hypothesis.
基于 RNA 干扰(RNAi)的靶向特定基因产物的疗法已经对临床医学产生了影响,有 16 种 FDA 批准的药物。目前正在评估针对降低血浆脂蛋白(a)[Lp(a)]水平的 RNAi 疗法。
在过去的 20 年中,基于 RNA 的疗法取得了重大进展,目前包括反义寡核苷酸(ASO)和小干扰 RNA(siRNA)。RNA 骨架的化学修饰和 siRNA 的缀合使肝细 胞中的基因沉默效率提高,从而开发出有效的降胆固醇疗法。多条证据表明 Lp(a)在动脉粥样硬化性心血管疾病中起因果作用,最近的分析表明,Lp(a)比低密度脂蛋白胆固醇(LDL-C)更具致动脉粥样硬化性。这些发现导致了“Lp(a)假说”,即降低 Lp(a)可能显著改善心血管结局。四种基于 RNA 的药物已完成早期临床试验,证明血浆 Lp(a)水平降低了>80%。目前正在进行这些药物的 3 期临床试验,以评估临床结局数据。
目前,已有四种基于 RNA 的药物被证明能有效显著降低血浆 Lp(a)水平。3 期临床试验的临床结局数据将评估 Lp(a)假说。