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HADH may be the target molecule of early vascular endothelial impairment in T2DM
BACKGROUND: Type 2 diabetes mellitus (T2DM) will significantly increase the risk of atherosclerosis (AS). Vascular endothelial cell dysfunction (VECD) is the foundation of AS. Early identification and intervention of VECD caused by T2DM can help us effectively delay or even suppress the occurrence o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399638/ https://www.ncbi.nlm.nih.gov/pubmed/36035955 http://dx.doi.org/10.3389/fcvm.2022.963916 |
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author | Ye, Haowen Wang, Ruxin Wei, Jinjing Wang, Ying Wang, Lihong Zhang, Xiaofang |
author_facet | Ye, Haowen Wang, Ruxin Wei, Jinjing Wang, Ying Wang, Lihong Zhang, Xiaofang |
author_sort | Ye, Haowen |
collection | PubMed |
description | BACKGROUND: Type 2 diabetes mellitus (T2DM) will significantly increase the risk of atherosclerosis (AS). Vascular endothelial cell dysfunction (VECD) is the foundation of AS. Early identification and intervention of VECD caused by T2DM can help us effectively delay or even suppress the occurrence of AS. METHODS: We downloaded the gene expression profiles from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) were identified in R software and weighted gene co-expression network analysis (WGCNA) was performed to further screen the target genes. In addition, we used the receiver operating characteristic curve (ROC curve) to verify the diagnostic efficiency of target genes. Finally, target genes were validated by quantitative polymerase chain reaction (qPCR). RESULTS: Four target genes (CLUH, COG4, HADH, and MPZL2) were discovered in early vascular endothelial impairment caused by T2DM through differential expression analysis and WGCNA. The ROC curve of target genes showed that HADH had the best diagnostic efficacy in VECD and AS. qPCR showed that the mRNA level expression of HADH and MPZL2 were decreased in human coronary artery endothelial cells (HCAECs) treated with high glucose and palmitic acid. CONCLUSION: HADH may be the target gene in early VECD caused by T2DM. |
format | Online Article Text |
id | pubmed-9399638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93996382022-08-25 HADH may be the target molecule of early vascular endothelial impairment in T2DM Ye, Haowen Wang, Ruxin Wei, Jinjing Wang, Ying Wang, Lihong Zhang, Xiaofang Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Type 2 diabetes mellitus (T2DM) will significantly increase the risk of atherosclerosis (AS). Vascular endothelial cell dysfunction (VECD) is the foundation of AS. Early identification and intervention of VECD caused by T2DM can help us effectively delay or even suppress the occurrence of AS. METHODS: We downloaded the gene expression profiles from the Gene Expression Omnibus (GEO). The differential expression genes (DEGs) were identified in R software and weighted gene co-expression network analysis (WGCNA) was performed to further screen the target genes. In addition, we used the receiver operating characteristic curve (ROC curve) to verify the diagnostic efficiency of target genes. Finally, target genes were validated by quantitative polymerase chain reaction (qPCR). RESULTS: Four target genes (CLUH, COG4, HADH, and MPZL2) were discovered in early vascular endothelial impairment caused by T2DM through differential expression analysis and WGCNA. The ROC curve of target genes showed that HADH had the best diagnostic efficacy in VECD and AS. qPCR showed that the mRNA level expression of HADH and MPZL2 were decreased in human coronary artery endothelial cells (HCAECs) treated with high glucose and palmitic acid. CONCLUSION: HADH may be the target gene in early VECD caused by T2DM. Frontiers Media S.A. 2022-08-10 /pmc/articles/PMC9399638/ /pubmed/36035955 http://dx.doi.org/10.3389/fcvm.2022.963916 Text en Copyright © 2022 Ye, Wang, Wei, Wang, Wang and Zhang. 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 | Cardiovascular Medicine Ye, Haowen Wang, Ruxin Wei, Jinjing Wang, Ying Wang, Lihong Zhang, Xiaofang HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title | HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title_full | HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title_fullStr | HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title_full_unstemmed | HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title_short | HADH may be the target molecule of early vascular endothelial impairment in T2DM |
title_sort | hadh may be the target molecule of early vascular endothelial impairment in t2dm |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399638/ https://www.ncbi.nlm.nih.gov/pubmed/36035955 http://dx.doi.org/10.3389/fcvm.2022.963916 |
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