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Updated: Sep 6, 2025

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Comparative study on the performance of different classification algorithms, combined with pre- and post-processing
João Albuquerque1,2,3, Ana Margarida Medeiros3,4, Ana Catarina Alves3,4
1Departamento de Biomedicina, Unidade de Bioquímica, Faculdade de Medicina, Universidade do Porto, Porto, Portugal.
Insights
This study introduces improved methods for diagnosing Familial Hypercholesterolemia (FH), an inherited cholesterol disorder. A logistic regression model combined with SMOTE offers a more accurate and interpretable screening tool than current criteria.
Area of Science:
- Medical Informatics
- Genetics
- Biochemistry
Background:
- Familial Hypercholesterolemia (FH) is a genetic disorder affecting cholesterol metabolism.
- Existing diagnostic criteria, such as the Simon Broome (SB) criteria, exhibit high false positive rates.
- There is a need for more accurate diagnostic procedures for FH.
Purpose of the Study:
- To develop and evaluate alternative classification methods for FH diagnosis.
- To compare machine learning algorithms with established criteria using biological and biochemical indicators.
- To identify an optimal model for widespread FH screening.
Main Methods:
- Employed logistic regression (LR), naive Bayes (NB), random forest (RF), and extreme gradient boosting (XGB) algorithms.
- Utilized Synthetic Minority Oversampling Technique (SMOTE) and Youden index (YI) for class imbalance.
- Performed 10x10 repeated k-fold cross-validation for robust testing.
Main Results:
- The LR model demonstrated superior performance (AUROC, AUPRC) irrespective of imbalance handling.
- All tested algorithms significantly outperformed SB criteria in accuracy, G-mean, and F1 score (p < 0.01).
- SMOTE-enhanced LR provided high sensitivity and maintained model interpretability.
Conclusions:
- Machine learning models, particularly LR with SMOTE, offer enhanced accuracy and balanced prediction for FH.
- These advanced methods significantly improve upon current diagnostic standards.
- An LR-SMOTE model is proposed as an effective tool for widespread FH screening.
Abstract:
Familial Hypercholesterolemia (FH) is an inherited disorder of cholesterol metabolism. Current criteria for FH diagnosis, like Simon Broome (SB) criteria, lead to high false positive rates. The aim of this work was to explore alternative classification procedures for FH diagnosis, based on different biological and biochemical indicators. For this purpose, logistic regression (LR), naive Bayes classifier (NB), random forest (RF) and extreme gradient boosting (XGB) algorithms were combined with Synthetic Minority Oversampling Technique (SMOTE), or threshold adjustment by maximizing Youden index (YI), and compared. Data was tested through a 10 × 10 repeated k-fold cross validation design. The LR model presented an overall better performance, as assessed by the areas under the receiver operating characteristics (AUROC) and precision-recall (AUPRC) curves, and several operating characteristics (OC), regardless of the strategy to cope with class imbalance. When adopting either data processing technique, significantly higher accuracy (Acc), G-mean and F1 score values were found for all classification algorithms, compared to SB criteria (p < 0.01), revealing a more balanced predictive ability for both classes, and higher effectiveness in classifying FH patients. Adjustment of the cut-off values through pre or post-processing methods revealed a considerable gain in sensitivity (Sens) values (p < 0.01). Although the performance of pre and post-processing strategies was similar, SMOTE does not cause model's parameters to loose interpretability. These results suggest a LR model combined with SMOTE can be an optimal approach to be used as a widespread screening tool.
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