A CpG-SNP Located within the ARPC3 Gene Promoter Is Associated with Hypertriglyceridemia in Severely Obese Patients

作者：de Toro Martin Juan; Guenard Frederic; Tchernof Andre; Deshaies Yves; Perusse Louis; Biron Simon; Lescelleur Odette; Biertho Laurent; Marceau Simon; Vohl Marie Claude^*

来源：Annals of Nutrition and Metabolism, 2016, 68(3): 203-212.

DOI：10.1159/000445358

• Actin-related protein 2/3 complex subunit 3
• Obesity
• Visceral adipose tissue
• CpG-SNP
• Metabolic syndrome
• Triglycerides

Aims: To test the potential association of cytosine-phosphate- guanine dinucleotides (CpG)-single-nucleotide polymorphisms (SNPs) located within actin-related protein 2/3 complex subunit 3 (ARPC3), a gene recently linked to adipogenesis and lipid accumulation, with metabolic syndrome (MetS) features in severely obese patients. Methods: Prioritized SNPs within the ARPC3 locus were genotyped and tested for associations with MetS features in a cohort of 1,749 obese patients with and without MetS. Association testing with CpG methylation levels was performed in a methylation sub-cohort of 16 obese men. Results: A significant association was found between the CpG-SNP rs3759384 (C>T) and plasma triglyceride (TG) levels (false discovery rate-corrected p = 3.5 x 10(-2)), with 0.6% of the phenotypic variance explained by the CpG-SNP, and with TT homozygotes showing the highest plasma TG levels (1.89 mmol/l). The carriers of the rs3759384 T allele also showed a significant decrease in methylation levels of the ARPC3 promoter-associated CpG site cg10738648 in both visceral adipose tissue and blood. ARPC3 expression levels showed a strong correlation with plasma TG levels (r = 0.70; p = 0.02). Conclusions: The increased plasma TG levels found in homozygous rs3759384 T allele carriers argue for a relevant role of this CpG-SNP in lipid management among obese individuals, which may be driven by an epigenetic-mediated mechanism.

• 出版日期2016