» Articles » PMID: 39565562

Inhibition of the ANGPTL3/8 Complex for the Prevention and Treatment of Atherosclerotic Cardiovascular Disease

Overview
Publisher Springer
Date 2024 Nov 20
PMID 39565562
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: Dyslipidemia is a casual risk factor for atherosclerotic cardiovascular disease (ASCVD). There is an unmet need for more effective treatments for patients with dyslipidemias. Angiopoietin-like protein 3 (ANGPTL3) and ANGPTL8 play key roles in triglyceride trafficking and energy balance in humans. We review the functional role of these ANGPTL proteins in the regulation of lipoprotein metabolism, and recent clinical trials targeting ANGPTL3 and ANGPTL3/8 with monoclonal antibody and/or nucleic acid therapies, including antisense oligonucleotides and small interfering RNA.

Recent Findings: Cumulative evidence supports the roles of ANGPTL3 and ANGPTL8 in lipid metabolism through inhibition of lipoprotein lipase and endothelial lipase activity. ANGPTL3 and ANGPTL3/8 inhibitors are effective in lowering plasma triglycerides and low-density lipoprotein (LDL)-cholesterol, with the possible advantage of raising high-density lipoprotein (HDL)-cholesterol with the inhibition of ANGPTL3/8. Therapeutic inhibition of ANGPTL3 and ANGPTL3/8 can lower plasma triglyceride and LDL-cholesterol levels possibly by lowering production and upregulating catabolism of triglyceride-rich lipoprotein and LDL particles. However, the effect of these novel agents on HDL metabolism remains unclear. The cardiovascular benefits of ANGPTL3 and ABGPTL3/8 inhibitors may also include improvement in vascular inflammation, but this requires further investigation.

Citing Articles

Current and Emerging Treatment Options for Hypertriglyceridemia: State-of-the-Art Review.

Zimodro J, Rizzo M, Gouni-Berthold I Pharmaceuticals (Basel). 2025; 18(2).

PMID: 40005962 PMC: 11858358. DOI: 10.3390/ph18020147.


Novel lipid profiles and atherosclerotic cardiovascular disease risk: insights from a latent profile analysis.

Wan H, Wu H, Wei Y, Wang S, Ji Y Lipids Health Dis. 2025; 24(1):71.

PMID: 40001219 PMC: 11854406. DOI: 10.1186/s12944-025-02471-3.


Prioritization of Lipid Metabolism Targets for the Diagnosis and Treatment of Cardiovascular Diseases.

Wang Z, Chen S, Zhang F, Akhmedov S, Weng J, Xu S Research (Wash D C). 2025; 8:0618.

PMID: 39975574 PMC: 11836198. DOI: 10.34133/research.0618.


An overview of persistent chylomicronemia: much more than meets the eye.

Larouche M, Watts G, Ballantyne C, Gaudet D Curr Opin Endocrinol Diabetes Obes. 2025; 32(2):75-88.

PMID: 39927417 PMC: 11872273. DOI: 10.1097/MED.0000000000000903.


The relationship between non-HDL-C/HDL-C ratio and bone mineral density: an NHANES study.

Qi S, Peng B, Xu Z, Qiu D, Tan G Front Nutr. 2025; 11():1486370.

PMID: 39839298 PMC: 11747152. DOI: 10.3389/fnut.2024.1486370.


References
1.
Mach F, Baigent C, Catapano A, Koskinas K, Casula M, Badimon L . 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. Eur Heart J. 2019; 41(1):111-188. DOI: 10.1093/eurheartj/ehz455. View

2.
Libby P, Hansson G . From Focal Lipid Storage to Systemic Inflammation: JACC Review Topic of the Week. J Am Coll Cardiol. 2019; 74(12):1594-1607. PMC: 6910128. DOI: 10.1016/j.jacc.2019.07.061. View

3.
Arnold N, Lechner K, Waldeyer C, Shapiro M, Koenig W . Inflammation and Cardiovascular Disease: The Future. Eur Cardiol. 2021; 16:e20. PMC: 8157394. DOI: 10.15420/ecr.2020.50. View

4.
Peng X, Wu H . Inflammatory Links Between Hypertriglyceridemia and Atherogenesis. Curr Atheroscler Rep. 2022; 24(5):297-306. PMC: 9575332. DOI: 10.1007/s11883-022-01006-w. View

5.
Watts G, Gidding S, Hegele R, Raal F, Sturm A, Jones L . International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia. Nat Rev Cardiol. 2023; 20(12):845-869. DOI: 10.1038/s41569-023-00892-0. View