<p>Accurate classification among Alzheimer’s Disease (AD), Fronto Temporal Dementia (FTD), and Cognitively Normal (CN) adults from EEG remains challenging. We propose a multi-class classification method that fuses interpretable spectral/connectivity biomarkers (band power, spectral entropy, <InlineEquation ID="IEq1"> <EquationSource Format="TEX">\(\alpha\)</EquationSource> </InlineEquation>-coherence) with compact temporal embeddings from a customized lightweight one Dimensional Convolutional Neural Network (1D-CNN). The fused features are reduced by Principal Component Analysis (PCA) and classified with Support Vector Machine (SVM). All data-dependent steps like Synthetic Minority Over Sampling Technique (SMOTE), z-scoring and PCA are fit strictly on training folds to prevent leakage. Hyperparameters including PCA dimensionality and SMOTE neighbors were selected via inner-loop grid sweeps that maximized macro-F1; full grids and class distributions before/after SMOTE (inner-train only) are reported in the Supplement. On OpenNeuro ds004504 (eyes-closed; <InlineEquation ID="IEq2"> <EquationSource Format="TEX">\(N{=}88\)</EquationSource> </InlineEquation>; 36 AD/23 FTD/29 CN) the model achieved 94.5% accuracy, macro-F1 <InlineEquation ID="IEq3"> <EquationSource Format="TEX">\(=0.95\)</EquationSource> </InlineEquation>, and AUC <InlineEquation ID="IEq4"> <EquationSource Format="TEX">\(=0.96\)</EquationSource> </InlineEquation>. Robustness was examined on two public datasets using the identical preprocessing/segmentation: (i) cross-condition testing on ds006036 (eyes-open recordings from the same participants) and (ii) zero-shot transfer to an independent OSF dataset with different instrumentation and demographics. SHapley Additive exPlanations (SHAP) analyses provided global, class-wise, and subject-level attributions aligned with known electrophysiology (e.g., reduced <InlineEquation ID="IEq5"> <EquationSource Format="TEX">\(\alpha\)</EquationSource> </InlineEquation>-coherence, elevated <InlineEquation ID="IEq6"> <EquationSource Format="TEX">\(\theta\)</EquationSource> </InlineEquation>), supporting clinical interpretability. These results indicate that a transparent hybrid feature design can deliver accurate, leakage-safe, and explainable EEG-based differentiation of AD, FTD, and CN with preliminary external checks.</p>

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A deep-SVM hybrid framework with enhanced EEG feature engineering and SHAP-based explainability for Alzheimer’s classification

  • Frnaz Akbar,
  • Yazeed Alkhrijah,
  • Syed Muhammad Usman,
  • Shehzad Khalid,
  • Imran Ihsan,
  • Mohamad A. Alawad

摘要

Accurate classification among Alzheimer’s Disease (AD), Fronto Temporal Dementia (FTD), and Cognitively Normal (CN) adults from EEG remains challenging. We propose a multi-class classification method that fuses interpretable spectral/connectivity biomarkers (band power, spectral entropy, \(\alpha\) -coherence) with compact temporal embeddings from a customized lightweight one Dimensional Convolutional Neural Network (1D-CNN). The fused features are reduced by Principal Component Analysis (PCA) and classified with Support Vector Machine (SVM). All data-dependent steps like Synthetic Minority Over Sampling Technique (SMOTE), z-scoring and PCA are fit strictly on training folds to prevent leakage. Hyperparameters including PCA dimensionality and SMOTE neighbors were selected via inner-loop grid sweeps that maximized macro-F1; full grids and class distributions before/after SMOTE (inner-train only) are reported in the Supplement. On OpenNeuro ds004504 (eyes-closed; \(N{=}88\) ; 36 AD/23 FTD/29 CN) the model achieved 94.5% accuracy, macro-F1 \(=0.95\) , and AUC \(=0.96\) . Robustness was examined on two public datasets using the identical preprocessing/segmentation: (i) cross-condition testing on ds006036 (eyes-open recordings from the same participants) and (ii) zero-shot transfer to an independent OSF dataset with different instrumentation and demographics. SHapley Additive exPlanations (SHAP) analyses provided global, class-wise, and subject-level attributions aligned with known electrophysiology (e.g., reduced \(\alpha\) -coherence, elevated \(\theta\) ), supporting clinical interpretability. These results indicate that a transparent hybrid feature design can deliver accurate, leakage-safe, and explainable EEG-based differentiation of AD, FTD, and CN with preliminary external checks.