Protease Variants, LDL, and Coronary Heart Disease
- 23 March 2006
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 354 (12) , 1310-1312
- https://doi.org/10.1056/nejme068026
Abstract
Just when we thought we understood everything about low-density lipoprotein (LDL) cholesterol and its relationship to cardiovascular risk, along comes a discovery that reveals a new control mechanism and suggests a strategy for the prevention of atherosclerotic cardiovascular disease.Plasma levels of LDL cholesterol are in large part determined by the activity of LDL receptors in the liver. Autosomal dominant familial hypercholesterolemia — with its high levels of LDL cholesterol, xanthomas, and premature atherosclerosis — is caused by mutations either in the gene encoding the LDL receptor or in the gene encoding apolipoprotein B — the protein in LDL cholesterol . . .Keywords
This publication has 5 references indexed in Scilit:
- Sequence Variations inPCSK9,Low LDL, and Protection against Coronary Heart DiseaseNew England Journal of Medicine, 2006
- Trends in Serum Lipids and Lipoproteins of Adults, 1960-2002JAMA, 2005
- Decreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9Proceedings of the National Academy of Sciences, 2005
- Overexpression of PCSK9 accelerates the degradation of the LDLR in a post-endoplasmic reticulum compartmentProceedings of the National Academy of Sciences, 2005
- Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9Nature Genetics, 2005