Regularized Machine Learning Models for Prediction of Metabolic Syndrome Using

Classification LASSO Machine Learning Metabolic syndrome Penalized Regression

Journal

Cell journal
ISSN: 2228-5806
Titre abrégé: Cell J
Pays: Iran
ID NLM: 101566618

Informations de publication

Date de publication:
01 Aug 2023
Historique:
received: 25 04 2023
medline: 29 8 2023
pubmed: 29 8 2023
entrez: 29 8 2023
Statut: epublish

Résumé

Metabolic syndrome (MetS) is a complex multifactorial disorder that considerably burdens healthcare systems. We aim to classify MetS using regularized machine learning models in the presence of the risk variants of A cohort study was conducted on 2,346 cases and 2,203 controls from eligible Tehran Cardiometabolic Genetic Study (TCGS) participants whose data were collected from 1999 to 2017. We used different regularization approaches [least absolute shrinkage and selection operator (LASSO), ridge regression (RR), elasticnet (ENET), adaptive LASSO (aLASSO), and adaptive ENET (aENET)] and a classical logistic regression (LR) model to classify MetS and select influential variables that predict MetS. Demographics, clinical features, and common polymorphisms in the During the follow-up period, 50.38% of participants developed MetS. The groups were not similar in terms of baseline characteristics and risk variants. MetS was significantly associated with age, gender, schooling years, body mass index (BMI), and alternate alleles in all the risk variants, as indicated by LR. A comparison of accuracy, AUCROC, and AUC-PR metrics indicated that the regularization models outperformed LR. Regularized machine learning models provided comparable classification performances, whereas the aLASSO model was more parsimonious and selected fewer predictors. Regularized machine learning models provided more accurate and parsimonious MetS classifying models. These high-performing diagnostic models can lay the foundation for clinical decision support tools that use genetic and demographical variables to locate individuals at high risk for MetS.

Identifiants

pubmed: 37641415
doi: 10.22074/cellj.2023.2000864.1294
pmc: PMC10542204
pii:
doi:

Types de publication

Journal Article

Langues

eng

Pagination

536-545

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Auteurs

Nadia Alipour (N)

Department of Biostatistics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Anoshirvan Kazemnejad (A)

Department of Biostatistics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran. Email: kazem_an@modares.ac.ir.

Mahdi Akbarzadeh (M)

Cellular and Molecular Endocrine Research Centre, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Farzad Eskandari (F)

Department of Statistics, Faculty of Statistics, Mathematics and Computer, Allameh Tabataba'i University, Tehran, Iran.

Asiyeh Sadat Zahedi (AS)

Cellular and Molecular Endocrine Research Centre, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Maryam S Daneshpour (MS)

Cellular and Molecular Endocrine Research Centre, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Email: daneshpour@sbmu.ac.ir.

Classifications MeSH