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

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 a...

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Autores principales: Portilla-Fernandez, Eliana, Ghanbari, Mohsen, van Meurs, Joyce B. J., Danser, A. H. Jan, Franco, Oscar H., Muka, Taulant, Roks, Anton, Dehghan, Abbas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433264/
https://www.ncbi.nlm.nih.gov/pubmed/30908504
http://dx.doi.org/10.1371/journal.pone.0214137
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author Portilla-Fernandez, Eliana
Ghanbari, Mohsen
van Meurs, Joyce B. J.
Danser, A. H. Jan
Franco, Oscar H.
Muka, Taulant
Roks, Anton
Dehghan, Abbas
author_facet Portilla-Fernandez, Eliana
Ghanbari, Mohsen
van Meurs, Joyce B. J.
Danser, A. H. Jan
Franco, Oscar H.
Muka, Taulant
Roks, Anton
Dehghan, Abbas
author_sort Portilla-Fernandez, Eliana
collection PubMed
description 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.
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spelling pubmed-64332642019-04-08 Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach Portilla-Fernandez, Eliana Ghanbari, Mohsen van Meurs, Joyce B. J. Danser, A. H. Jan Franco, Oscar H. Muka, Taulant Roks, Anton Dehghan, Abbas PLoS One Research Article 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. Public Library of Science 2019-03-25 /pmc/articles/PMC6433264/ /pubmed/30908504 http://dx.doi.org/10.1371/journal.pone.0214137 Text en © 2019 Portilla-Fernandez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Portilla-Fernandez, Eliana
Ghanbari, Mohsen
van Meurs, Joyce B. J.
Danser, A. H. Jan
Franco, Oscar H.
Muka, Taulant
Roks, Anton
Dehghan, Abbas
Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title_full Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title_fullStr Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title_full_unstemmed Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title_short Dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: A population-based approach
title_sort dissecting the association of autophagy-related genes with cardiovascular diseases and intermediate vascular traits: a population-based approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433264/
https://www.ncbi.nlm.nih.gov/pubmed/30908504
http://dx.doi.org/10.1371/journal.pone.0214137
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