Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.

<h4>Background</h4>Rupture of abdominal aortic aneurysm (rAAA) is a fatal event in the elderly. Elevated blood pressure and weakening of vessel wall strength are major risk factors for this devastating event. This present study examined whether the expression profile of mechanosensitive...

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Main Authors: Chang Sheng, Qin Zeng, Weihua Huang, Mingmei Liao, Pu Yang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2024-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0296729&type=printable
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author Chang Sheng
Qin Zeng
Weihua Huang
Mingmei Liao
Pu Yang
author_facet Chang Sheng
Qin Zeng
Weihua Huang
Mingmei Liao
Pu Yang
author_sort Chang Sheng
collection DOAJ
description <h4>Background</h4>Rupture of abdominal aortic aneurysm (rAAA) is a fatal event in the elderly. Elevated blood pressure and weakening of vessel wall strength are major risk factors for this devastating event. This present study examined whether the expression profile of mechanosensitive genes correlates with the phenotype and outcome, thus, serving as a biomarker for AAA development.<h4>Methods</h4>In this study, we identified mechanosensitive genes involved in AAA development using general bioinformatics methods and machine learning with six human datasets publicly available from the GEO database. Differentially expressed mechanosensitive genes (DEMGs) in AAAs were identified by differential expression analysis. Molecular biological functions of genes were explored using functional clustering, Protein-protein interaction (PPI), and weighted gene co-expression network analysis (WGCNA). According to the datasets (GSE98278, GSE205071 and GSE165470), the changes of diameter and aortic wall strength of AAA induced by DEMGs were verified by consensus clustering analysis, machine learning models, and statistical analysis. In addition, a model for identifying AAA subtypes was built using machine learning methods.<h4>Results</h4>38 DEMGs clustered in pathways regulating 'Smooth muscle cell biology' and 'Cell or Tissue connectivity'. By analyzing the GSE205071 and GSE165470 datasets, DEMGs were found to respond to differences in aneurysm diameter and vessel wall strength. Thus, in the merged datasets, we formally created subgroups of AAAs and found differences in immune characteristics between the subgroups. Finally, a model that accurately predicts the AAA subtype that is more likely to rupture was successfully developed.<h4>Conclusion</h4>We identified 38 DEMGs that may be involved in AAA. This gene cluster is involved in regulating the maximum vessel diameter, degree of immunoinflammatory infiltration, and strength of the local vessel wall in AAA. The prognostic model we developed can accurately identify the AAA subtypes that tend to rupture.
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spelling doaj.art-e1ab0917ca8d444f8b62a464e17e69dc2024-02-17T05:32:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032024-01-01192e029672910.1371/journal.pone.0296729Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.Chang ShengQin ZengWeihua HuangMingmei LiaoPu Yang<h4>Background</h4>Rupture of abdominal aortic aneurysm (rAAA) is a fatal event in the elderly. Elevated blood pressure and weakening of vessel wall strength are major risk factors for this devastating event. This present study examined whether the expression profile of mechanosensitive genes correlates with the phenotype and outcome, thus, serving as a biomarker for AAA development.<h4>Methods</h4>In this study, we identified mechanosensitive genes involved in AAA development using general bioinformatics methods and machine learning with six human datasets publicly available from the GEO database. Differentially expressed mechanosensitive genes (DEMGs) in AAAs were identified by differential expression analysis. Molecular biological functions of genes were explored using functional clustering, Protein-protein interaction (PPI), and weighted gene co-expression network analysis (WGCNA). According to the datasets (GSE98278, GSE205071 and GSE165470), the changes of diameter and aortic wall strength of AAA induced by DEMGs were verified by consensus clustering analysis, machine learning models, and statistical analysis. In addition, a model for identifying AAA subtypes was built using machine learning methods.<h4>Results</h4>38 DEMGs clustered in pathways regulating 'Smooth muscle cell biology' and 'Cell or Tissue connectivity'. By analyzing the GSE205071 and GSE165470 datasets, DEMGs were found to respond to differences in aneurysm diameter and vessel wall strength. Thus, in the merged datasets, we formally created subgroups of AAAs and found differences in immune characteristics between the subgroups. Finally, a model that accurately predicts the AAA subtype that is more likely to rupture was successfully developed.<h4>Conclusion</h4>We identified 38 DEMGs that may be involved in AAA. This gene cluster is involved in regulating the maximum vessel diameter, degree of immunoinflammatory infiltration, and strength of the local vessel wall in AAA. The prognostic model we developed can accurately identify the AAA subtypes that tend to rupture.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0296729&type=printable
spellingShingle Chang Sheng
Qin Zeng
Weihua Huang
Mingmei Liao
Pu Yang
Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
PLoS ONE
title Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
title_full Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
title_fullStr Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
title_full_unstemmed Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
title_short Identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes.
title_sort identification of abdominal aortic aneurysm subtypes based on mechanosensitive genes
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0296729&type=printable
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AT puyang identificationofabdominalaorticaneurysmsubtypesbasedonmechanosensitivegenes