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A Hybrid Model for Psoriasis Subtype Classification: Integrating Multi Transfer Learning and Hard Voting Ensemble Models

Diagnostics (Basel). 2024 Dec 28;15(1):55. doi: 10.3390/diagnostics15010055.

ABSTRACT

Background: Psoriasis is a chronic, immune-mediated skin disease characterized by lifelong persistence and fluctuating symptoms. The clinical similarities among its subtypes and the diversity of symptoms present challenges in diagnosis. Early diagnosis plays a vital role in preventing the spread of lesions and improving patients' quality of life. Methods: This study proposes a hybrid model combining multiple transfer learning and ensemble learning methods to classify psoriasis subtypes accurately and efficiently. The dataset includes 930 images labeled by expert dermatologists from the Dermatology Clinic of Fırat University Hospital, representing four distinct subtypes: generalized, guttate, plaque, and pustular. Class imbalance was addressed by applying synthetic data augmentation techniques, particularly for the rare subtype. To reduce the influence of nonlesion environmental factors, the images underwent systematic cropping and preprocessing steps, such as Gaussian blur, thresholding, morphological operations, and contour detection. DenseNet-121, EfficientNet-B0, and ResNet-50 transfer learning models were utilized to extract feature vectors, which were then combined to form a unified feature set representing the strengths of each model. The feature set was divided into 80% training and 20% testing subsets and evaluated using a hard voting classifier consisting of logistic regression, random forest, support vector classifier, k-nearest neighbors, and gradient boosting algorithms. Results: The proposed hybrid approach achieved 93.14% accuracy, 96.75% precision, and an F1 score of 91.44%, demonstrating superior performance compared to individual transfer learning models. Conclusions: This method offers significant potential to enhance the classification of psoriasis subtypes in clinical and real-world settings.

PMID:39795583 | DOI:10.3390/diagnostics15010055

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