| Literature DB >> 34974612 |
Lale Tokgozoglu1, Carl Orringer2, Henry N Ginsberg3, Alberico L Catapano4.
Abstract
The past year was an exciting time for clinical lipidology when we learnt more about existing therapies as well as therapies targeting novel pathways discovered through genetic studies. LDL cholesterol remained the main target and a variety of drugs to lower LDL cholesterol through different mechanisms were explored. Emerging evidence on the atherogenity of triglyceride-rich lipoproteins led to renewed interest in lowering them with new treatments. Lp(a) was back in focus with evidence on causality and new targeted therapeutics which dramatically lower Lp(a) levels. We will be able to personalise lipid lowering therapy further with this enriched armamentarium once we have the results of the cardiovascular outcome studies with some of these new agents.Entities:
Keywords: Antisense; CRISPR; Cardiovascular diseases; LDL-C. Triglycerides; Lipids; Lp(a); Nucleic acid therapeutics; PCSK9 inhibitors; RNA interference; Statins
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Year: 2022 PMID: 34974612 DOI: 10.1093/eurheartj/ehab875
Source DB: PubMed Journal: Eur Heart J ISSN: 0195-668X Impact factor: 29.983