Genetics
CETP-HDL association is one of only four gene-lipid-trait pairs replicated using a new cardiovascular gene chip in a multiethnic cohort (J Lipid Res 2009)
Original title: Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample
This study sought to replicate genome-wide-association-study loci for plasma triglycerides, HDL-cholesterol, and LDL-cholesterol using the Illumina cardiovascular disease beadchip, containing about 50,000 SNPs across roughly 2,100 genes, in a multiethnic population-based cohort of European (n=272), South Asian (n=330), and Chinese (n=304) ancestry. Identity-by-state clustering successfully classified individuals by self-reported ethnicity. Strong associations (P less than 2x10-6) were identified between triglycerides and APOA5, triglycerides and LPL, HDL-cholesterol and CETP, and LDL-cholesterol and APOE. Across 13 loci, associations with the same or a proxy SNP were replicated in the same direction as previously reported (P less than 0.05). A cumulative risk-allele count across replicated SNPs improved explained lipoprotein variance beyond traditional variables like age, sex, BMI, and ethnicity. The authors highlight the utility of the beadchip while noting the need for meta-analysis across commonly studied cohorts.
Original abstract
Recent genome-wide association studies (GWAS) have reproducibly identified loci associated with plasma triglycerides (TG), HDL cholesterol, and LDL cholesterol. We sought to replicate these findings in a multiethnic population-based cohort using the curated single nucleotide polymorphism (SNP) set found on the new Illumina cardiovascular disease (CVD) beadchip, which contains approximately 50,000 SNPs densely mapping approximately 2,100 genes, selected based on their potential role in CVD. The sample consisted of individuals with European (n = 272), South Asian (n = 330), and Chinese (n = 304) ancestry. Identity by state clustering successfully classified individuals according to self-reported ethnicities. Associations between TG and APOA5, TG and LPL, HDL and CETP, and LDL and APOE were all identified (P < 2 x 10(-6)). In 13 loci, associations with the same SNP or a proxy SNP were identified in the same direction as previously reported (P < 0.05). Assessing the cumulative number of risk-associated alleles at multiple replicated SNPs increased the proportion of explained lipoprotein variance over and above traditional variables such as age, sex, body mass index, and ethnicity. The findings indicate the potential utility of the Illumina CVD beadchip, but they underscore the need to consider meta-analysis of results from commonly studied clinical or epidemiological samples.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.