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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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 |
work_keys_str_mv |
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