A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics

Early risk assessments and interventions for metabolic syndrome (MetS) are limited because of a lack of effective biomarkers. In the present study, several candidate genes were selected as a blood-based transcriptomic signature for MetS. We collected so far the largest MetS-associated peripheral blo...

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Main Authors: Guanzhi Liu, Sen Luo, Yutian Lei, Jianhua Wu, Zhuo Huang, Kunzheng Wang, Pei Yang, Xin Huang
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Bioengineered
Subjects:
Online Access:http://dx.doi.org/10.1080/21655979.2021.1968249
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spelling doaj-472dd3e0fb1b4069b2d87faa7439440a2021-09-20T13:17:22ZengTaylor & Francis GroupBioengineered2165-59792165-59872021-01-011215727573810.1080/21655979.2021.19682491968249A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformaticsGuanzhi Liu0Sen Luo1Yutian Lei2Jianhua Wu3Zhuo Huang4Kunzheng Wang5Pei Yang6Xin Huang7Second Affiliated Hospital of Xi’an Jiaotong UniversitySecond Affiliated Hospital of Xi’an Jiaotong UniversitySecond Affiliated Hospital of Xi’an Jiaotong UniversityFirst Affiliated Hospital of Xi’an Jiaotong UniversitySecond Affiliated Hospital of Xi’an Jiaotong UniversitySecond Affiliated Hospital of Xi’an Jiaotong UniversitySecond Affiliated Hospital of Xi’an Jiaotong UniversityFirst Affiliated Hospital of Xi’an Jiaotong UniversityEarly risk assessments and interventions for metabolic syndrome (MetS) are limited because of a lack of effective biomarkers. In the present study, several candidate genes were selected as a blood-based transcriptomic signature for MetS. We collected so far the largest MetS-associated peripheral blood high-throughput transcriptomics data and put forward a novel feature selection strategy by combining weighted gene co-expression network analysis, protein-protein interaction network analysis, LASSO regression and random forest approaches. Two gene modules and 51 hub genes as well as a 9-hub-gene signature associated with metabolic syndrome were identified. Then, based on this 9-hub-gene signature, we performed logistic analysis and subsequently established a web nomogram calculator for metabolic syndrome risk (https://xjtulgz.shinyapps.io/DynNomapp/). This 9-hub-gene signature showed excellent classification and calibration performance (AUC = 0.968 in training set, AUC = 0.883 in internal validation set, AUC = 0.861 in external validation set) as well as ideal potential clinical benefit.http://dx.doi.org/10.1080/21655979.2021.1968249machine learningmetabolic syndromebioinformaticsbiomarkersgene hub
collection DOAJ
language English
format Article
sources DOAJ
author Guanzhi Liu
Sen Luo
Yutian Lei
Jianhua Wu
Zhuo Huang
Kunzheng Wang
Pei Yang
Xin Huang
spellingShingle Guanzhi Liu
Sen Luo
Yutian Lei
Jianhua Wu
Zhuo Huang
Kunzheng Wang
Pei Yang
Xin Huang
A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
Bioengineered
machine learning
metabolic syndrome
bioinformatics
biomarkers
gene hub
author_facet Guanzhi Liu
Sen Luo
Yutian Lei
Jianhua Wu
Zhuo Huang
Kunzheng Wang
Pei Yang
Xin Huang
author_sort Guanzhi Liu
title A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
title_short A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
title_full A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
title_fullStr A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
title_full_unstemmed A nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
title_sort nine-hub-gene signature of metabolic syndrome identified using machine learning algorithms and integrated bioinformatics
publisher Taylor & Francis Group
series Bioengineered
issn 2165-5979
2165-5987
publishDate 2021-01-01
description Early risk assessments and interventions for metabolic syndrome (MetS) are limited because of a lack of effective biomarkers. In the present study, several candidate genes were selected as a blood-based transcriptomic signature for MetS. We collected so far the largest MetS-associated peripheral blood high-throughput transcriptomics data and put forward a novel feature selection strategy by combining weighted gene co-expression network analysis, protein-protein interaction network analysis, LASSO regression and random forest approaches. Two gene modules and 51 hub genes as well as a 9-hub-gene signature associated with metabolic syndrome were identified. Then, based on this 9-hub-gene signature, we performed logistic analysis and subsequently established a web nomogram calculator for metabolic syndrome risk (https://xjtulgz.shinyapps.io/DynNomapp/). This 9-hub-gene signature showed excellent classification and calibration performance (AUC = 0.968 in training set, AUC = 0.883 in internal validation set, AUC = 0.861 in external validation set) as well as ideal potential clinical benefit.
topic machine learning
metabolic syndrome
bioinformatics
biomarkers
gene hub
url http://dx.doi.org/10.1080/21655979.2021.1968249
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