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Author
- Bell, Thomas A III1
- Boot, Manon1
- Christodoulides, Constantinos1
- Crooke, Rosanne M1
- Dollé, Martijn ET1
- Donner, Aaron J1
- Ibi, Dorina1
- Jukema, J Wouter1
- Karpe, Fredrik1
- Koivula, Robert1
- Lee, Richard G1
- Liu, Mingxia1
- Mullick, Adam E1
- Neville, Matt J1
- Noordam, Raymond1
- Rensen, Patrick CN1
- Rosendaal, Frits R1
- Willems van Dijk, Ko1
Regular Research Articles
2 Results
- Research ArticleOpen Access
Apolipoprotein A-V is a potential target for treating coronary artery disease: evidence from genetic and metabolomic analyses
Journal of Lipid ResearchVol. 63Issue 5100193Published online: March 9, 2022- Dorina Ibi
- Manon Boot
- Martijn E.T. Dollé
- J. Wouter Jukema
- Frits R. Rosendaal
- Constantinos Christodoulides
- and others
Cited in Scopus: 1Triglyceride (TG)-lowering LPL variants in combination with genetic LDL-C-lowering variants are associated with reduced risk of coronary artery disease (CAD). Genetic variation in the APOA5 gene encoding apolipoprotein A-V also strongly affects TG levels, but the potential clinical impact and underlying mechanisms are yet to be resolved. Here, we aimed to study the effects of APOA5 genetic variation on CAD risk and plasma lipoproteins through factorial genetic association analyses. Using data from 309,780 European-ancestry participants from the UK Biobank, we evaluated the effects of lower TG levels as a result of genetic variation in APOA5 and/or LPL on CAD risk with or without a background of reduced LDL-C. - Research ArticleOpen Access
Antisense oligonucleotide–mediated inhibition of angiopoietin-like protein 3 increases reverse cholesterol transport in mice
Journal of Lipid ResearchVol. 62100101Published online: August 5, 2021- Thomas A. Bell III
- Mingxia Liu
- Aaron J. Donner
- Richard G. Lee
- Adam E. Mullick
- Rosanne M. Crooke
Cited in Scopus: 0Supported by an abundance of experimental and genetic evidence, angiopoietin-like protein 3 (ANGPTL3) has emerged as a promising therapeutic target for cardiovascular disease. ANGPTL3 is primarily produced by the liver and is a potent modulator of plasma lipids and lipoproteins. Experimental models and subjects with loss-of-function Angptl3 mutations typically present with lower levels of HDL-C than noncarriers. The effect of ANGPTL3 on HDL-C is typically attributed to its function as an inhibitor of the enzyme endothelial lipase.