Association of DNA Methylation at CPT1A Locus with Metabolic Syndrome in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) Study

PLoS One. 2016 Jan 25;11(1):e0145789. doi: 10.1371/journal.pone.0145789. eCollection 2016.

Abstract

In this study, we conducted an epigenome-wide association study of metabolic syndrome (MetS) among 846 participants of European descent in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). DNA was isolated from CD4+ T cells and methylation at ~470,000 cytosine-phosphate-guanine dinucleotide (CpG) pairs was assayed using the Illumina Infinium HumanMethylation450 BeadChip. We modeled the percentage methylation at individual CpGs as a function of MetS using linear mixed models. A Bonferroni-corrected P-value of 1.1 x 10(-7) was considered significant. Methylation at two CpG sites in CPT1A on chromosome 11 was significantly associated with MetS (P for cg00574958 = 2.6x10(-14) and P for cg17058475 = 1.2x10(-9)). Significant associations were replicated in both European and African ancestry participants of the Bogalusa Heart Study. Our findings suggest that methylation in CPT1A is a promising epigenetic marker for MetS risk which could become useful as a treatment target in the future.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Anthropometry
  • Black People / genetics
  • Black or African American
  • Blood Pressure
  • Carnitine O-Palmitoyltransferase / genetics*
  • Carnitine O-Palmitoyltransferase / physiology
  • Chromosomes, Human, Pair 11 / genetics
  • Cohort Studies
  • CpG Islands / genetics*
  • DNA Methylation*
  • Female
  • Humans
  • Male
  • Metabolic Syndrome / ethnology
  • Metabolic Syndrome / genetics*
  • Middle Aged
  • Minnesota / epidemiology
  • Oligonucleotide Array Sequence Analysis
  • Risk Factors
  • Triglycerides / blood
  • Utah / epidemiology
  • White People / genetics

Substances

  • Triglycerides
  • CPT1A protein, human
  • Carnitine O-Palmitoyltransferase