4.3 Article

Opening the black box: interpretable machine learning for predictor finding of metabolic syndrome

Journal

BMC ENDOCRINE DISORDERS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12902-022-01121-4

Keywords

Metabolic syndrome; Data mining; Machine learning; Model interpretability; Risk prediction model

Funding

  1. National Natural Science Foundation of China [71663053]

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This study analyzes the predictive models of metabolic syndrome and applies model interpretability methods to identify associations with other factors. The results provide a flexible and interpretable approach to identify risk factors associated with MetS.
Objective: The internal workings ofmachine learning algorithms are complex and considered as low-interpretation black box models, making it difficult for domain experts to understand and trust these complex models. The study uses metabolic syndrome (MetS) as the entry point to analyze and evaluate the application value of model interpretability methods in dealing with difficult interpretation of predictive models. Methods: The study collects data from a chain of health examination institution in Urumqi from 2017 similar to 2019, and performs 39,134 remaining data after preprocessing such as deletion and filling. RFE is used for feature selection to reduce redundancy; MetS risk prediction models (logistic, random forest, XGBoost) are built based on a feature subset, and accuracy, sensitivity, specificity, Youden index, and AUROC value are used to evaluate the model classification performance; post-hoc model-agnostic interpretation methods (variable importance, LIME) are used to interpret the results of the predictive model. Results: Eighteen physical examination indicators are screened out by RFE, which can effectively solve the problem of physical examination data redundancy. Random forest and XGBoost models have higher accuracy, sensitivity, specificity, Youden index, and AUROC values compared with logistic regression. XGBoost models have higher sensitivity, Youden index, and AUROC values compared with random forest. The study uses variable importance, LIME and PDP for global and local interpretation of the optimal MetS risk prediction model (XGBoost), and different interpretation methods have different insights into the interpretation of model results, which are more flexible in model selection and can visualize the process and reasons for the model to make decisions. The interpretable risk prediction model in this study can help to identify risk factors associated with MetS, and the results showed that in addition to the traditional risk factors such as overweight and obesity, hyperglycemia, hypertension, and dyslipidemia, MetS was also associated with other factors, including age, creatinine, uric acid, and alkaline phosphatase. Conclusion: The model interpretability methods are applied to the black box model, which can not only realize the flexibility of model application, but also make up for the uninterpretable defects of the model. Model interpretability methods can be used as a novel means of identifying variables that are more likely to be good predictors.

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