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MicroRNAs and Cardiovascular Disease in Diabetes Mellitus

Cardiovascular disease (CVD) is the major macrovascular complication of diabetes mellitus. Recently, although CVD morbidity and mortality have decreased as a result of comprehensive control of CVD risk factors, CVD remains the leading cause of death of patients with diabetes in many countries, indic...

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Detalles Bibliográficos
Autores principales: Ding, Yue, Sun, Xue, Shan, Peng-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337313/
https://www.ncbi.nlm.nih.gov/pubmed/28299324
http://dx.doi.org/10.1155/2017/4080364
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author Ding, Yue
Sun, Xue
Shan, Peng-Fei
author_facet Ding, Yue
Sun, Xue
Shan, Peng-Fei
author_sort Ding, Yue
collection PubMed
description Cardiovascular disease (CVD) is the major macrovascular complication of diabetes mellitus. Recently, although CVD morbidity and mortality have decreased as a result of comprehensive control of CVD risk factors, CVD remains the leading cause of death of patients with diabetes in many countries, indicating the potential underlying pathophysiological mechanisms. MicroRNAs are a class of noncoding, single-stranded RNA molecules that are involved in β-cell function, insulin secretion, insulin resistance, skeletal muscle, and adipose tissue and which play an important role in glucose homeostasis and the pathogenesis of diabetic complications. Here, we review recent progress in research on microRNAs in endothelial cell and vascular smooth muscle cell dysfunction, macrophage and platelet activation, lipid metabolism abnormality, and cardiomyocyte repolarization in diabetes mellitus. We also review the progress of microRNAs as potential biomarkers and therapeutic targets of CVD in patients with diabetes.
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spelling pubmed-53373132017-03-15 MicroRNAs and Cardiovascular Disease in Diabetes Mellitus Ding, Yue Sun, Xue Shan, Peng-Fei Biomed Res Int Review Article Cardiovascular disease (CVD) is the major macrovascular complication of diabetes mellitus. Recently, although CVD morbidity and mortality have decreased as a result of comprehensive control of CVD risk factors, CVD remains the leading cause of death of patients with diabetes in many countries, indicating the potential underlying pathophysiological mechanisms. MicroRNAs are a class of noncoding, single-stranded RNA molecules that are involved in β-cell function, insulin secretion, insulin resistance, skeletal muscle, and adipose tissue and which play an important role in glucose homeostasis and the pathogenesis of diabetic complications. Here, we review recent progress in research on microRNAs in endothelial cell and vascular smooth muscle cell dysfunction, macrophage and platelet activation, lipid metabolism abnormality, and cardiomyocyte repolarization in diabetes mellitus. We also review the progress of microRNAs as potential biomarkers and therapeutic targets of CVD in patients with diabetes. Hindawi Publishing Corporation 2017 2017-02-12 /pmc/articles/PMC5337313/ /pubmed/28299324 http://dx.doi.org/10.1155/2017/4080364 Text en Copyright © 2017 Yue Ding et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ding, Yue
Sun, Xue
Shan, Peng-Fei
MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title_full MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title_fullStr MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title_full_unstemmed MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title_short MicroRNAs and Cardiovascular Disease in Diabetes Mellitus
title_sort micrornas and cardiovascular disease in diabetes mellitus
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337313/
https://www.ncbi.nlm.nih.gov/pubmed/28299324
http://dx.doi.org/10.1155/2017/4080364
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