Lightweight deep learning for medical imaging using MobileNetV2-based brain pathology classification with Grad-CAM interpretability.
Overview
- Department of Computing, University of Derby, Derby, United Kingdom
- Department of Information Technology, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia
- Department of Management Information Systems, College of Business and Economics, Qassim University, Saudi Arabia
- Faculty of Computing and Information, Al-Baha University, Al-Baha, Saudi Arabia
- Redcad Laboratory, University of Sfax, Sfax, Tunisia
Abstract
Introduction: Computed Tomography (CT) brain scans are crucial for diagnosing various neurological conditions, including tumors, cancer, and aneurysms. CT brain scans are essential for guiding treatment decisions and monitoring disease progression. In this study, we propose a novel framework for brain CT image classification that leverages convolutional neural networks (CNNs), Digital Imaging and Communications in Medicine (DICOM) pre-processing, transfer learning with multiple deep models, and ensemble prediction techniques. The primary objective is to enhance the accuracy and interpretability of brain abnormality detection.
Methods: Our approach uses a comprehensive dataset of CT brain scans that undergo meticulous pre-processing to ensure data integrity and uniformity, and employs Grad-CAM for interpretability. We employ four state-of-the-art pre-trained models: MobileNetV2, ResNet-50, EfficientNet-B0, and VGG-16, each serving as a feature extractor, followed by a classification head tailored to our specific task.
Results: The experimental results demonstrate that MobileNetV2 and the Ensemble model achieved the highest classification accuracy of 97.44% with macro-AUC scores of 0.9895 and 0.9914, respectively, followed by VGG16 with 92.31% accuracy and the highest macro-AUC of 0.9962. In contrast, ResNet50 and EfficientNetB0 achieved accuracies of 61.54% and 33.33%, respectively, indicating fundamental limitations in learning discriminative features for this medical imaging task. MobileNetV2 proved to be the most efficient model, achieving superior accuracy with training and test times of 89 s and 38.16 s, respectively.
Discussion: MobileNetV2 is highly suitable for clinical deployment where both accuracy and computational efficiency are critical.
Reproduced under the paper's license (CC BY), from the paper cited above.
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Data
Datasets cited
- kaggle.com/
datasets/ , at Kaggle; found in the end of the papertrainingdatapro
Data availability statement
The original contributions presented in the study are included in the article/
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
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Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, pages, dates, 5 authors, 5 keywords, 41 references.
Cite
This paper
Sattar, M. U., Alamro, M. A., Mihoub, A., Aljarboa, S., & Krichen, M. (2026). Lightweight deep learning for medical imaging using MobileNetV2-based brain pathology classification with Grad-CAM interpretability. Frontiers in medicine, 13, 1810860. https://
BibTeX
@article{sattar2026light
author = {Sattar, Mian Usman and Alamro, Meznah A. and Mihoub, Alaeddine and Aljarboa, Soliman and Krichen, Moez},
title = {{Lightweight deep learning for medical imaging using MobileNetV2-based brain pathology classification with Grad-CAM interpretability}},
journal = {Frontiers in medicine},
year = {2026},
month = may,
volume = {13},
pages = {1810860},
publisher = {Frontiers Media SA},
issn = {2296-858X},
doi = {10.3389/
url = {https://
pmid = {42338932},
pmcid = {PMC13284855}
}
RIS
TY - JOUR
AU - Sattar, Mian Usman
AU - Alamro, Meznah A.
AU - Mihoub, Alaeddine
AU - Aljarboa, Soliman
AU - Krichen, Moez
TI - Lightweight deep learning for medical imaging using MobileNetV2-based brain pathology classification with Grad-CAM interpretability
T2 - Frontiers in medicine
J2 - Front Med (Lausanne)
PY - 2026
DA - 2026/
VL - 13
SP - 1810860
SN - 2296-858X
PB - Frontiers Media SA
DO - 10.3389/
UR - https://
LA - en
ER -
CSL-JSON
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