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Epigenetics of methylation modifications in diabetic cardiomyopathy

Type 2 diabetes is one of the most common metabolic diseases with complications including diabetic cardiomyopathy and atherosclerotic cardiovascular disease. Recently, a growing body of research has revealed that the complex interplay between epigenetic changes and the environmental factors may sign...

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Detalles Bibliográficos
Autores principales: Hao, Jing, Liu, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050754/
https://www.ncbi.nlm.nih.gov/pubmed/37008904
http://dx.doi.org/10.3389/fendo.2023.1119765
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author Hao, Jing
Liu, Yao
author_facet Hao, Jing
Liu, Yao
author_sort Hao, Jing
collection PubMed
description Type 2 diabetes is one of the most common metabolic diseases with complications including diabetic cardiomyopathy and atherosclerotic cardiovascular disease. Recently, a growing body of research has revealed that the complex interplay between epigenetic changes and the environmental factors may significantly contribute to the pathogenesis of cardiovascular complications secondary to diabetes. Methylation modifications, including DNA methylation and histone methylation among others, are important in developing diabetic cardiomyopathy. Here we summarized the literatures of studies focusing on the role of DNA methylation, and histone modifications in microvascular complications of diabetes and discussed the mechanism underlying these disorders, to provide the guidance for future research toward an integrated pathophysiology and novel therapeutic strategies to treat or prevent this frequent pathological condition.
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spelling pubmed-100507542023-03-30 Epigenetics of methylation modifications in diabetic cardiomyopathy Hao, Jing Liu, Yao Front Endocrinol (Lausanne) Endocrinology Type 2 diabetes is one of the most common metabolic diseases with complications including diabetic cardiomyopathy and atherosclerotic cardiovascular disease. Recently, a growing body of research has revealed that the complex interplay between epigenetic changes and the environmental factors may significantly contribute to the pathogenesis of cardiovascular complications secondary to diabetes. Methylation modifications, including DNA methylation and histone methylation among others, are important in developing diabetic cardiomyopathy. Here we summarized the literatures of studies focusing on the role of DNA methylation, and histone modifications in microvascular complications of diabetes and discussed the mechanism underlying these disorders, to provide the guidance for future research toward an integrated pathophysiology and novel therapeutic strategies to treat or prevent this frequent pathological condition. Frontiers Media S.A. 2023-03-15 /pmc/articles/PMC10050754/ /pubmed/37008904 http://dx.doi.org/10.3389/fendo.2023.1119765 Text en Copyright © 2023 Hao and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Hao, Jing
Liu, Yao
Epigenetics of methylation modifications in diabetic cardiomyopathy
title Epigenetics of methylation modifications in diabetic cardiomyopathy
title_full Epigenetics of methylation modifications in diabetic cardiomyopathy
title_fullStr Epigenetics of methylation modifications in diabetic cardiomyopathy
title_full_unstemmed Epigenetics of methylation modifications in diabetic cardiomyopathy
title_short Epigenetics of methylation modifications in diabetic cardiomyopathy
title_sort epigenetics of methylation modifications in diabetic cardiomyopathy
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050754/
https://www.ncbi.nlm.nih.gov/pubmed/37008904
http://dx.doi.org/10.3389/fendo.2023.1119765
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