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Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study


Cadby, G and Melton, PE and McCarthy, NS and Giles, C and Mellett, NA and Huynh, K and Hung, J and Beilby, J and Dube, M-P and Watts, GF and Blangero, J and Meikle, PJ and Moses, EK, Heritability of 596 lipid species and genetic correlation with cardiovascular traits in the Busselton Family Heart Study, Journal of Lipid Research, 61, (4) pp. 537-545. ISSN 0022-2275 (2020) [Refereed Article]

Copyright Statement

Copyright 2020 Cadby et al.

DOI: doi:10.1194/jlr.RA119000594


CVD is the leading cause of death worldwide, and genetic investigations into the human lipidome may provide insight into CVD risk. The aim of this study was to estimate the heritability of circulating lipid species and their genetic correlation with CVD traits. Targeted lipidomic profiling was performed on 4,492 participants from the Busselton Family Heart Study to quantify the major fatty acids of 596 lipid species from 33 classes. We estimated narrow-sense heritabilities of lipid species/classes and their genetic correlations with eight CVD traits: BMI, HDL-C, LDL-C, triglycerides, total cholesterol, waist-hip ratio, systolic blood pressure, and diastolic blood pressure. We report heritabilities and genetic correlations of new lipid species/subclasses, including acylcarnitine (AC), ubiquinone, sulfatide, and oxidized cholesteryl esters. Over 99% of lipid species were significantly heritable (h2: 0.06-0.50) and all lipid classes were significantly heritable (h2: 0.14-0.50). The monohexosylceramide and AC classes had the highest median heritabilities (h2 = 0.43). The largest genetic correlation was between clinical triglycerides and total diacylglycerol (rg = 0.88). We observed novel positive genetic correlations between clinical triglycerides and phosphatidylglycerol species (rg: 0.64-0.82), and HDL-C and alkenylphosphatidylcholine species (rg: 0.45-0.74). Overall, 51% of the 4,768 lipid species-CVD trait genetic correlations were statistically significant after correction for multiple comparisons. This is the largest lipidomic study to address the heritability of lipids and their genetic correlation with CVD traits. Future work includes identifying putative causal genetic variants for lipid species and CVD using genome-wide SNP and whole-genome sequencing data.

Item Details

Item Type:Refereed Article
Keywords:cardiovascular disease, lipidomics, lipids
Research Division:Biological Sciences
Research Group:Genetics
Research Field:Gene mapping
Objective Division:Health
Objective Group:Clinical health
Objective Field:Clinical health not elsewhere classified
UTAS Author:Melton, PE (Dr Phillip Melton)
UTAS Author:Moses, EK (Professor Eric Moses)
ID Code:141373
Year Published:2020
Web of Science® Times Cited:13
Deposited By:Menzies Institute for Medical Research
Deposited On:2020-10-16
Last Modified:2022-08-25

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