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An epigenome-wide association study of metabolic syndrome and its components
by
Järvelin, Marjo-Riitta
, Joensuu, Anni
, Jousilahti, Pekka
, Milani, Lili
, Pervjakova, Natalia
, Kristiansson, Kati
, Nuotio, Marja-Liisa
, Karhunen, Ville
, Kettunen, Johannes
, Perola, Markus
, Hiekkalinna, Tero
, Salomaa, Veikko
, Metspalu, Andres
in
631/208/176/1988
/ 692/308/2056
/ Adult
/ Aged
/ ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics
/ Cardiovascular diseases
/ Carrier Proteins - genetics
/ Chromosome 1
/ Chromosome 21
/ Diabetes
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ DNA methylation
/ DNA Methylation - genetics
/ Epigenesis, Genetic - genetics
/ Epigenome - genetics
/ Epigenomics - methods
/ Female
/ Finland - epidemiology
/ Genome - genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Glucose
/ Glucose - metabolism
/ High density lipoprotein
/ Humanities and Social Sciences
/ Humans
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Lipids - genetics
/ Male
/ Metabolic disorders
/ Metabolic syndrome
/ Metabolic Syndrome - genetics
/ Metabolic Syndrome - metabolism
/ Methylation
/ Middle Aged
/ multidisciplinary
/ Polymorphism, Single Nucleotide - genetics
/ Science
/ Science (multidisciplinary)
/ Triglycerides
/ White People - genetics
2020
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An epigenome-wide association study of metabolic syndrome and its components
by
Järvelin, Marjo-Riitta
, Joensuu, Anni
, Jousilahti, Pekka
, Milani, Lili
, Pervjakova, Natalia
, Kristiansson, Kati
, Nuotio, Marja-Liisa
, Karhunen, Ville
, Kettunen, Johannes
, Perola, Markus
, Hiekkalinna, Tero
, Salomaa, Veikko
, Metspalu, Andres
in
631/208/176/1988
/ 692/308/2056
/ Adult
/ Aged
/ ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics
/ Cardiovascular diseases
/ Carrier Proteins - genetics
/ Chromosome 1
/ Chromosome 21
/ Diabetes
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ DNA methylation
/ DNA Methylation - genetics
/ Epigenesis, Genetic - genetics
/ Epigenome - genetics
/ Epigenomics - methods
/ Female
/ Finland - epidemiology
/ Genome - genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Glucose
/ Glucose - metabolism
/ High density lipoprotein
/ Humanities and Social Sciences
/ Humans
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Lipids - genetics
/ Male
/ Metabolic disorders
/ Metabolic syndrome
/ Metabolic Syndrome - genetics
/ Metabolic Syndrome - metabolism
/ Methylation
/ Middle Aged
/ multidisciplinary
/ Polymorphism, Single Nucleotide - genetics
/ Science
/ Science (multidisciplinary)
/ Triglycerides
/ White People - genetics
2020
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An epigenome-wide association study of metabolic syndrome and its components
by
Järvelin, Marjo-Riitta
, Joensuu, Anni
, Jousilahti, Pekka
, Milani, Lili
, Pervjakova, Natalia
, Kristiansson, Kati
, Nuotio, Marja-Liisa
, Karhunen, Ville
, Kettunen, Johannes
, Perola, Markus
, Hiekkalinna, Tero
, Salomaa, Veikko
, Metspalu, Andres
in
631/208/176/1988
/ 692/308/2056
/ Adult
/ Aged
/ ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics
/ Cardiovascular diseases
/ Carrier Proteins - genetics
/ Chromosome 1
/ Chromosome 21
/ Diabetes
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ DNA methylation
/ DNA Methylation - genetics
/ Epigenesis, Genetic - genetics
/ Epigenome - genetics
/ Epigenomics - methods
/ Female
/ Finland - epidemiology
/ Genome - genetics
/ Genome-Wide Association Study - methods
/ Genomes
/ Glucose
/ Glucose - metabolism
/ High density lipoprotein
/ Humanities and Social Sciences
/ Humans
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Lipids - genetics
/ Male
/ Metabolic disorders
/ Metabolic syndrome
/ Metabolic Syndrome - genetics
/ Metabolic Syndrome - metabolism
/ Methylation
/ Middle Aged
/ multidisciplinary
/ Polymorphism, Single Nucleotide - genetics
/ Science
/ Science (multidisciplinary)
/ Triglycerides
/ White People - genetics
2020
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An epigenome-wide association study of metabolic syndrome and its components
Journal Article
An epigenome-wide association study of metabolic syndrome and its components
2020
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Overview
The role of metabolic syndrome (MetS) as a preceding metabolic state for type 2 diabetes and cardiovascular disease is widely recognised. To accumulate knowledge of the pathological mechanisms behind the condition at the methylation level, we conducted an epigenome-wide association study (EWAS) of MetS and its components, testing 1187 individuals of European ancestry for approximately 470 000 methylation sites throughout the genome. Methylation site cg19693031 in gene
TXNIP
—previously associated with type 2 diabetes, glucose and lipid metabolism, associated with fasting glucose level (
P
= 1.80 × 10
−8
). Cg06500161 in gene
ABCG1
associated both with serum triglycerides (
P
= 5.36 × 10
−9
) and waist circumference (
P
= 5.21 × 10
−9
). The previously identified type 2 diabetes–associated locus cg08309687 in chromosome 21 associated with waist circumference for the first time (
P
= 2.24 × 10
−7
). Furthermore, a novel HDL association with cg17901584 in chromosome 1 was identified (
P
= 7.81 × 10
−8
). Our study supports previous genetic studies of MetS, finding that lipid metabolism plays a key role in pathology of the syndrome. We provide evidence regarding a close interplay with glucose metabolism. Finally, we suggest that in attempts to identify methylation loci linking separate MetS components, cg19693031 appears to represent a strong candidate.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Adult
/ Aged
/ ATP Binding Cassette Transporter, Subfamily G, Member 1 - genetics
/ Diabetes
/ Diabetes mellitus (non-insulin dependent)
/ Diabetes Mellitus, Type 2 - genetics
/ Epigenesis, Genetic - genetics
/ Female
/ Genome-Wide Association Study - methods
/ Genomes
/ Glucose
/ Humanities and Social Sciences
/ Humans
/ Male
/ Metabolic Syndrome - genetics
/ Metabolic Syndrome - metabolism
/ Polymorphism, Single Nucleotide - genetics
/ Science
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