Journal Article

Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

Oddsson, Asmundur, Masson, Gisli, Thorleifsson, Gudmar, Patel, Riyaz S, Thorgeirsson, Gudmundur, Helgadottir, Anna, Azizi, Fereidoun, Kiemeney, Lambertus, Swinkels, Dorine W, Quyyumi, Arshed A, Sveinbjornsson, Gardar, Hjartarson, Eirikur, Magnusdottir, Audur, Thorsteinsdottir, Unnur, Steinthorsdottir, Valgerdur, Olafsson, Isleifur, Rafnar, Thorunn, Gudbjartsson, Daniel F, Hayek, Salim S, Holm, Hilma, Daneshpour, Maryam S, Kristjansson, Helgi, Eyjolfsson, Gudmundur I, Stefansson, Kari, Sulem, Patrick, Jonsdottir, Ingileif, Jonasdottir, Aslaug, Sigurdardottir, Olof, Sigurdsson, Asgeir, Levey, Allan I, Gretarsdottir, Solveig, Khalili, Davood, Gudmundsdottir, Ingibjorg J

2016

Overview

Kari Stefansson and colleagues report discovery of 13 variants with large effects on non-HDL cholesterol, LDL cholesterol, HDL cholesterol or triglyceride lipid fractions. They further show that, among these lipid fractions, the non-HDL cholesterol genetic risk score associates most strongly with coronary disease and confers risk beyond that of LDL cholesterol and that, after accounting for non-HDL cholesterol, neither HDL cholesterol nor triglyceride genetic risk scores associate with coronary disease. Sequence variants affecting blood lipids and coronary artery disease (CAD) may enhance understanding of the atherogenicity of lipid fractions. Using a large resource of whole-genome sequence data, we examined rare and low-frequency variants for association with non-HDL cholesterol, HDL cholesterol, LDL cholesterol, and triglycerides in up to 119,146 Icelanders. We discovered 13 variants with large effects (within ANGPTL3 , APOB , ABCA1 , NR1H3 , APOA1 , LIPC , CETP , LDLR , and APOC1 ) and replicated 14 variants. Five variants within PCSK9 , APOA1 , ANGPTL4 , and LDLR associate with CAD (33,090 cases and 236,254 controls). We used genetic risk scores for the lipid fractions to examine their causal relationship with CAD. The non-HDL cholesterol genetic risk score associates most strongly with CAD ( P = 2.7 × 10 −28 ), and no other genetic risk score associates with CAD after accounting for non-HDL cholesterol. The genetic risk score for non-HDL cholesterol confers CAD risk beyond that of LDL cholesterol ( P = 5.5 × 10 −8 ), suggesting that targeting atherogenic remnant cholesterol may reduce cardiovascular risk.

• Publisher: Nature Publishing Group US,Nature Publishing Group
• Subject: 45/43 / 631/208/205/2138 / 631/208/457 / 692/308/2056 / 692/699/75/2099 / Agriculture / Analysis / Animal Genetics and Genomics / Biomedicine / Blood / Blood lipids / Cancer Research / Cholesterol / Cholesterol - blood / Coronary Artery Disease - blood / Coronary Artery Disease - diagnosis / Coronary Artery Disease - genetics / Coronary heart disease / Epidemiology / Fatty acids / Gene Function / Genomes / Health risks / Human Genetics / Humans / Lipids / Lipids - blood / Low density lipoprotein / Mutation / Pathogenesis / Population / Risk factors / Studies / Triglycerides / Triglycerides - blood