Martin Hazael Guerrero Flores

Dr. Martin Hazael Guerrero Flores


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 December 2019
Verified
Book Chapter
Closed access
PDF file
MFMartin Hazael Guerrero Flores
Martin Hazael Guerrero Flores
Huizilopoztli Luna-GarcíaHuizilopoztli Luna-García
Huizilopoztli Luna-García
Carlos Eric Galván-TejadaCarlos Eric Galván-Tejada
Carlos Eric Galván-Tejada
HGHamurabi Gamboa
Hamurabi Gamboa
JPJose Maria Padilla
Jose Maria Padilla
MCMiguel A. De la Cruz
Miguel A. De la Cruz

23 December 2025 in Diagnostics
Verified
Journal Article
Open access
PDF file
MFMartin Hazael Guerrero Flores
Martin Hazael Guerrero Flores
VMValeria Maeda-Gutiérrez
Valeria Maeda-Gutiérrez
Carlos Eric Galván-TejadaCarlos Eric Galván-Tejada
Carlos Eric Galván-Tejada
Carlos Eric Galván-TejadaCarlos Eric Galván-Tejada
Carlos Eric Galván-Tejada
MCMiguel Cruz
Miguel Cruz
JSJavier Saldivar
Javier Saldivar
Background: Type 2 diabetes (T2D) is a growing public health problem in Mexico. Lipid profile alterations have been shown to appear years before changes in glycemic biomarkers, and some of the latter are limited in availability, especially in underserved settings. Therefore, anthropometric variables and lipids represent relevant early indicators for the early detection of the disease. This study evaluates the capacity of non-glycemic clinical data—including lipid profile and anthropometric indicators—to detect T2D using machine learning, and compares the performance of different feature engineering approaches. Methods: Using more than a thousand clinical records of Mexican adults, three experiments were developed: (1) a distribution and normality analysis to characterize the variability of lipid variables; (2) an evaluation of the predictive power of multiple atherogenic indices (Castelli I, Castelli II, TG/HDL, and AIP); and (3) the implementation of statistical transformations (logarithmic, quare-root, and Z-standardization) to stabilize variance and improve feature quality. Logistic regression, SVM-RBF, random forest, and XGBoost models were trained on each feature set and evaluated using accuracy, sensitivity, specificity, F1-score, and area under the ROC curve. Results: The AIP index showed the greatest discriminatory power among the atherogenic indices, while normality-based transformations improved the performance of distribution-sensitive models, such as SVM. In the final experiment, the SVM-RBF and XGBoost models achieved AUC values greater than 0.90, demonstrating the feasibility of a diagnostic approach based exclusively on non-glycemic data. Conclusions: The findings indicate that the transformed lipid profile and anthropometric variables can constitute a solid and accessible alternative for the early detection of T2D in clinical and public health contexts, offering a robust methodological framework for future predictive applications in the absence of traditional glycemic biomarkers.