DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D

Type 1 diabetes (T1D) is an autoimmune disease that leads to insulin deficiency and hyperglycemia. Little is known about how this metabolic dysfunction, which substantially alters the internal environment, forces cells to adapt through epigenetic mechanisms. Consequently, the purpose of this work wa...

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Main Authors: Raúl F Pérez, Juan Luis Fernandez-Morera, Judit Romano-Garcia, Edelmiro Menendez-Torre, Elias Delgado-Alvarez, Mario F Fraga, Agustin F Fernandez
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Biomedicines
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Online Access:https://www.mdpi.com/2227-9059/9/1/13
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author Raúl F Pérez
Juan Luis Fernandez-Morera
Judit Romano-Garcia
Edelmiro Menendez-Torre
Elias Delgado-Alvarez
Mario F Fraga
Agustin F Fernandez
author_facet Raúl F Pérez
Juan Luis Fernandez-Morera
Judit Romano-Garcia
Edelmiro Menendez-Torre
Elias Delgado-Alvarez
Mario F Fraga
Agustin F Fernandez
author_sort Raúl F Pérez
collection DOAJ
description Type 1 diabetes (T1D) is an autoimmune disease that leads to insulin deficiency and hyperglycemia. Little is known about how this metabolic dysfunction, which substantially alters the internal environment, forces cells to adapt through epigenetic mechanisms. Consequently, the purpose of this work was to study what changes occur in the epigenome of T1D patients after the onset of disease and in the context of poor metabolic control. We performed a genome-wide analysis of DNA methylation patterns in blood samples from 18 T1D patients with varying levels of metabolic control. We identified T1D-associated DNA methylation differences on more than 100 genes when compared with healthy controls. Interestingly, only T1D patients displaying poor glycemic control showed epigenetic age acceleration compared to healthy controls. The epigenetic alterations identified in this work make a valuable contribution to improving our understanding of T1D and to ensuring the appropriate management of the disease in relation to maintaining healthy aging.
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spelling doaj.art-c1ffa90ce3e1458ca186a17ec340c38d2023-11-21T02:30:02ZengMDPI AGBiomedicines2227-90592020-12-01911310.3390/biomedicines9010013DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1DRaúl F Pérez0Juan Luis Fernandez-Morera1Judit Romano-Garcia2Edelmiro Menendez-Torre3Elias Delgado-Alvarez4Mario F Fraga5Agustin F Fernandez6Nanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), Institute of Oncology of Asturias (IUOPA), and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 33011 Oviedo, Asturias, SpainNanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), Institute of Oncology of Asturias (IUOPA), and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 33011 Oviedo, Asturias, SpainServicio de Anestesiologia y Reanimacion, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Asturias, SpainEndocrinology and Nutrition Department, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Asturias, SpainEndocrinology and Nutrition Department, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Asturias, SpainNanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), Institute of Oncology of Asturias (IUOPA), and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 33011 Oviedo, Asturias, SpainNanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), Institute of Oncology of Asturias (IUOPA), and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 33011 Oviedo, Asturias, SpainType 1 diabetes (T1D) is an autoimmune disease that leads to insulin deficiency and hyperglycemia. Little is known about how this metabolic dysfunction, which substantially alters the internal environment, forces cells to adapt through epigenetic mechanisms. Consequently, the purpose of this work was to study what changes occur in the epigenome of T1D patients after the onset of disease and in the context of poor metabolic control. We performed a genome-wide analysis of DNA methylation patterns in blood samples from 18 T1D patients with varying levels of metabolic control. We identified T1D-associated DNA methylation differences on more than 100 genes when compared with healthy controls. Interestingly, only T1D patients displaying poor glycemic control showed epigenetic age acceleration compared to healthy controls. The epigenetic alterations identified in this work make a valuable contribution to improving our understanding of T1D and to ensuring the appropriate management of the disease in relation to maintaining healthy aging.https://www.mdpi.com/2227-9059/9/1/13type 1 diabetesDNA methylationPhenoAgeepigenetic agingage accelerationmetabolic control
spellingShingle Raúl F Pérez
Juan Luis Fernandez-Morera
Judit Romano-Garcia
Edelmiro Menendez-Torre
Elias Delgado-Alvarez
Mario F Fraga
Agustin F Fernandez
DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
Biomedicines
type 1 diabetes
DNA methylation
PhenoAge
epigenetic aging
age acceleration
metabolic control
title DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
title_full DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
title_fullStr DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
title_full_unstemmed DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
title_short DNA Methylomes and Epigenetic Age Acceleration Associations with Poor Metabolic Control in T1D
title_sort dna methylomes and epigenetic age acceleration associations with poor metabolic control in t1d
topic type 1 diabetes
DNA methylation
PhenoAge
epigenetic aging
age acceleration
metabolic control
url https://www.mdpi.com/2227-9059/9/1/13
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