Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach

PLoS One. 2019 Mar 25;14(3):e0214137. doi: 10.1371/journal.pone.0214137. eCollection 2019.

Abstract

Autophagy is involved in cellular homeostasis and maintenance and may play a role in cardiometabolic health. We aimed to elucidate the role of autophagy in cardiometabolic traits by investigating genetic variants and DNA methylation in autophagy-related genes in relation to cardiovascular diseases and related traits. To address this research question, we implemented a multidirectional approach using several molecular epidemiology tools, including genetic association analysis with genome wide association studies data and exome sequencing data and differential DNA methylation analysis. We investigated the 21 autophagy-related genes in relation to coronary artery disease and a number of cardiometabolic traits (blood lipids, blood pressure, glycemic traits, type 2 diabetes). We used data from the largest genome wide association studies as well as DNA methylation and exome sequencing data from the Rotterdam Study. Single-nucleotide polymorphism rs110389913 in AMBRA1 (p-value = 4.9×10-18) was associated with blood proinsulin levels, whereas rs6587988 in ATG4C and rs10439163 in ATG4D with lipid traits (ATG4C: p-value = 2.5×10-15 for total cholesterol and p-value = 3.1×10-18 for triglycerides, ATG4D: p-value = 9.9×10-12 for LDL and p-value = 1.3×10-10 for total cholesterol). Moreover, rs7635838 in ATG7 was associated with HDL (p-value = 1.9×10-9). Rs2447607 located in ATG7 showed association with systolic blood pressure and pulse pressure. Rs2424994 in MAP1LC3A was associated with coronary artery disease (p-value = 5.8×10-6). Furthermore, we identified association of an exonic variant located in ATG3 with diastolic blood pressure (p-value = 6.75×10-6). Using DNA methylation data, two CpGs located in ULK1 (p-values = 4.5×10-7 and 1×10-6) and two located in ATG4B (2×10-13 and 1.48×10-7) were significantly associated with both systolic and diastolic blood pressure. In addition one CpG in ATG4D was associated with HDL (p-value = 3.21×10-5). Our findings provide support for the role of autophagy in glucose and lipid metabolism, as well as blood pressure regulation.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Autophagy*
  • Autophagy-Related Protein 7 / genetics
  • Autophagy-Related Protein-1 Homolog / genetics
  • Autophagy-Related Proteins / genetics
  • Coronary Artery Disease / genetics*
  • CpG Islands
  • Cysteine Endopeptidases / genetics
  • DNA Methylation
  • Exome Sequencing
  • Female
  • Genome-Wide Association Study
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Lipid Metabolism / genetics*
  • Male
  • Microtubule-Associated Proteins / genetics
  • Polymorphism, Single Nucleotide*
  • Quantitative Trait, Heritable*

Substances

  • AMBRA1 protein, human
  • Adaptor Proteins, Signal Transducing
  • Autophagy-Related Proteins
  • Intracellular Signaling Peptides and Proteins
  • MAP1LC3A protein, human
  • Microtubule-Associated Proteins
  • Autophagy-Related Protein-1 Homolog
  • ULK1 protein, human
  • ATG4A protein, human
  • ATG4B protein, human
  • ATG4D protein, human
  • Cysteine Endopeptidases
  • ATG7 protein, human
  • Autophagy-Related Protein 7

Grants and funding

The Rotterdam Study is funded by Erasmus Medical Center and Erasmus University, Rotterdam; Netherlands Organization for the Health Research and Development (ZonMw); the Research Institute for Diseases in the Elderly (RIDE); the Ministry of Education, Culture and Science; the Ministry for Health, Welfare and Sports; the European Commission (DG XII).