Therapeutic Targets of Triglyceride Metabolism as Informed by Human Genetics

Trends Mol Med. 2016 Apr;22(4):328-340. doi: 10.1016/j.molmed.2016.02.005. Epub 2016 Mar 14.

Abstract

Human genetics has contributed to the development of multiple drugs to treat hyperlipidemia and coronary artery disease (CAD), most recently including antibodies targeting PCSK9 to reduce LDL cholesterol. Despite these successes, a large burden of CAD remains. Genetic and epidemiological studies have suggested that circulating triglyceride (TG)-rich lipoproteins (TRLs) are a causal risk factor for CAD, presenting an opportunity for novel therapeutic strategies. We discuss recent unbiased human genetics testing, including genome-wide association studies (GWAS) and whole-genome or -exome sequencing, that have identified the lipoprotein lipase (LPL) and hepatic lipogenesis pathways as important mechanisms in the regulation of circulating TRLs. Further strengthening the causal relationship between TRLs and CAD, findings such as these may provide novel targets for much-needed potential therapeutic interventions.

Keywords: GWAS; genetics; lipogenesis; triglycerides.

Publication types

  • Review

MeSH terms

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Coronary Artery Disease / drug therapy
  • Coronary Artery Disease / etiology
  • Coronary Artery Disease / metabolism
  • Coronary Artery Disease / prevention & control
  • Gene Expression Regulation
  • Genome-Wide Association Study
  • Humans
  • Hydrolysis
  • Lipid Metabolism / drug effects*
  • Lipogenesis
  • Lipoproteins / blood
  • Lipoproteins / metabolism
  • Liver / metabolism
  • Molecular Targeted Therapy
  • Risk Factors
  • Signal Transduction
  • Toll-Like Receptors / metabolism
  • Triglycerides / blood
  • Triglycerides / metabolism*

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Lipoproteins
  • Toll-Like Receptors
  • Triglycerides