4.5 Review

Novel emerging therapies in atherosclerosis targeting lipid metabolism

Journal

EXPERT OPINION ON INVESTIGATIONAL DRUGS
Volume 29, Issue 6, Pages 611-622

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/13543784.2020.1764937

Keywords

Atherosclerosis; bempedoic acid; inclisiran; pemafibrate; PCSK9 inhibitors; IMPROVE-IT; FOURIER; ODYSSEY; ORION-10; CLEAR harmony; lomitapide; evinacumab; pemfibrate; REDUCE-IT; EVAPORATE

Funding

  1. NIHR Imperial Biomedical Research Centre
  2. NIHR Applied Research Collaboration for North West London, UK

Ask authors/readers for more resources

Introduction Recent years have brought significant developments in lipid and atherosclerosis research. Although statins are a cornerstone in hyperlipidemia management, new non-statin therapies have had an impact. The reduction of low-density lipoprotein cholesterol (LDL-C) further translates into the lowering of cardiovascular mortality. Additionally, lipid research has progressed beyond LDL-C reduction and this has brought triglyceride (TG) and other apoprotein-B containing lipids into focus. Areas covered Inclisiran and pemafibrate, with expected approval soon, come under the spotlight. We discuss other therapeutics such as lomitapide, mipomersen, volanesorsen, and evinacumab and newly approved non-statin-based therapies such as ezetimibe, icosapent ethyl (IPE), and bempedoic acid. Expert Opinion New options now exist for the prevention of atherosclerosis in patients that are not optimized on statin therapy. Multiple guidelines endorse ezetimibe, PCSK9 inhibitors, bempedoic, and IPE as add-on therapy. Recently approved bempedoic acid/ezetimibe combination might gain popularity among clinicians. Inclisiran and pemafibrate show promise in the reduction of LDL-C and TG, respectively, and results are pending in cardiovascular outcome trials. Combination strategies could improve outcomes, but the challenge will be balancing cost and selecting the correct patient population for each treatment modality to maximize benefit with the fewest medications.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available