The class
Review names CETP among four validated targets for novel lipid-lowering therapies to prevent cardiovascular disease (Nat Rev Cardiol 2023)
Original title: Novel and future lipid-modulating therapies for the prevention of cardiovascular disease
This review discusses novel and upcoming therapeutic strategies targeting lipid metabolism pathways beyond LDL-cholesterol lowering to reduce atherosclerotic cardiovascular disease risk, given evidence implicating triglyceride-rich lipoproteins, HDL, and lipoprotein(a) in atherosclerosis. It identifies PCSK9, angiopoietin-related protein 3, CETP, and apolipoprotein(a) as key proteins validated as therapeutic targets through observational and genetic studies, targetable via protein inhibition, mRNA-level interference with antisense oligonucleotides or small interfering RNA, or loss-of-function mutations introduced by base editing. The review argues these approaches are complementary to, and may eventually replace, existing daily small-molecule regimens, offering a path to durable reductions in causal cardiovascular exposures.
Original abstract
Lowering the levels of LDL cholesterol in the plasma has been shown to reduce the risk of atherosclerotic cardiovascular disease (ASCVD). Several other lipoproteins, such as triglyceride-rich lipoproteins, HDL and lipoprotein(a) are associated with atherosclerosis and ASCVD, with strong evidence supporting causality for some. In this Review, we discuss novel and upcoming therapeutic strategies targeting different pathways in lipid metabolism to potentially attenuate the risk of cardiovascular events. Key proteins involved in lipoprotein metabolism, such as PCSK9, angiopoietin-related protein 3, cholesteryl ester transfer protein and apolipoprotein(a), have been identified as viable targets for therapeutic intervention through observational and genetic studies. These proteins can be targeted using a variety of approaches, such as protein inhibition or interference, inhibition of translation at the mRNA level (with the use of antisense oligonucleotides or small interfering RNA), and the introduction of loss-of-function mutations through base editing. These novel and upcoming strategies are complementary to and could work synergistically with existing therapies, or in some cases could potentially replace therapies, offering unprecedented opportunities to prevent ASCVD. Moreover, a major challenge in the prevention and treatment of non-communicable diseases is how to achieve safe, long-lasting reductions in causal exposures. This challenge might be overcome with approaches such as small interfering RNAs or genome editing, which shows how far the field has advanced from when the burden of achieving this goal was placed upon patients through rigorous adherence to daily small-molecule drug regimens.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.