Background/Objectives: The increasing prevalence of diabetes underscores the urgent need for non-invasive, rapid, and cost-effective diagnostic alternatives. This study presents a breath-based multiclass diabetes classification system leveraging only three gas sensors (CO, alcohol, and acetone) to analyze exhaled breath composition. Methods: Breath samples were collected from 58 participants (22 healthy, 7 prediabetic, and 29 diabetic), with blood glucose levels serving as the reference metric. To enhance classification performance, we introduced a novel biomarker, the alcohol-to-acetone ratio, through a feature engineering approach. Class imbalance was addressed using the Synthetic Minority Over-Sampling Technique (SMOTE), ensuring a balanced dataset for model training. A nested cross-validation framework with 3 outer and 3 inner folds was implemented. Multiple machine learning classifiers were evaluated, with Random Forest and Gradient Boosting emerging as the top-performing models. Results: An ensemble combining both yielded the highest overall performance, achieving an average accuracy of 98.86%, precision of 99.07%, recall of 98.81% and F1 score of 98.87%. These findings highlight the potential of gas sensor-based breath analysis as a highly accurate, scalable, and non-invasive method for diabetes screening. Conclusions: The proposed system offers a promising alternative to blood-based diagnostic approaches, paving the way for real-world applications in point-of-care diagnostics and continuous health monitoring.
30 December 2024 in Journal of Research and Development
Lung and colon cancers are among the most common and lethal types of cancer. It is possible for individuals to develop both cancers simultaneously, as risk factors such as smoking, which is a leading cause of lung cancer, can also contribute to poor dietary habits, thereby increasing the risk of colon cancer. Traditionally, the diagnosis of these cancers relies on biopsies and subsequent laboratory analysis. This study proposes an Inception-ResNetV2-based model for accurately classifying lung and colon cancer using histopathological images. The dataset analyzed consists of 25,000 images categorized into five cancer types: Colon Adenocarcinoma, Colon Benign Tissue, Lung Adenocarcinoma, Lung Benign Tissue, and Lung Squamous Cell Carcinoma. The developed approach achieved an accuracy of 99.15%. The model's performance is further enhanced through the use of Local Binary Patterns (LBP), improving both accuracy and computational efficiency. Additionally, the explainable AI method SHAP is employed to demonstrate the contribution of each feature to the predictive analysis
Non-invasive blood glucose estimation from exhaled breath has been proposed as a painless alternative to repeated capillary measurements; however, performance evaluation remains challenging in small-sample settings. This study investigates the estimation of blood glucose from human breath using volatile organic compound (VOC) signals acquired with an electronic nose. Responses from three metal-oxide sensor channels sensitive to CO, alcohol, and acetone were collected from 58 individuals, with one measurement per subject, and analyzed using strictly patient-level five-fold cross-validation, in which test folds comprised only real subjects. Two experimental factors were examined. First, model performance was evaluated with and without an additional interpretable alcohol–acetone log-ratio capturing relative variation between compounds. Second, model training was performed using either real data only or fold-wise tabular synthetic augmentation generated via a Gaussian copula fitted exclusively on training subjects, while evaluation remained strictly real-only. Under real-only training, classical machine learning models achieved the lowest prediction errors (approximately 6–7 mg/dL), whereas under synthetic augmentation FTTransformer was the best-performing deep learning model. This findings should be understood as a constrained proof-of-concept analysis rather than as evidence of diagnostic capability or clinical readiness.