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Optimizing depression diagnosis: fNIRS and machine learning differentiate unipolar, bipolar, and healthy states
Jiayun Zhu1, Boyuan Wu1, Lan Mou2
1School of Information Engineering, Huzhou University, Huzhou, China.
Background:
Differentiating Unipolar Depression (UD) from Bipolar Depression (BD) remains challenging due to overlapping symptoms, which can lead to misdiagnosis and inappropriate treatment. fNIRS provides a portable, objective measure of prefrontal cortical activity, yet its utility for clinically relevant ternary classification (UD, BD, HC) remains underexplored.
Methods:
Prefrontal hemodynamics signals were recorded using 22-channel fNIRS during a verbal fluency task in 171 participants (UD = 72, BD = 59, HC = 40). Six classical machine learning models (Support Vector Machine, Random Forest, XGBoost, Logistic Regression, Naive Bayes, Decision Tree) and two deep learning models (1D-CNN, LSTM) were evaluated for ternary classification using whole-brain (FULL) features and eight prefrontal subregions. All models underwent hyperparameter optimization, stratified 5-fold cross-validation with class-weight adjustment, and data augmentation. Performance metrics included accuracy, sensitivity, specificity, and area under the ROC curve (AUC).
Results:
SVM achieved the highest FULL-region accuracy (80.19 %). FULL integration outperformed single-region models by 14.51 % average accuracy. Among subregions, the orbitofrontal cortex (OFC) contributed most to classification performance (average left OFC accuracy: 67.40 %). UD was most reliably identified, whereas BD frequently overlapped with HC, reflecting intrinsic neurophysiological similarity. Deep learning models achieved moderate performance, consistent with limited sample size and high feature dimensionality.
Conclusions:
fNIRS-based machine learning reliably differentiates UD, BD, and HC at the group level. Whole-brain integration yields superior performance, with OFC as a key discriminative region. SVM and Random Forest offer the best balance of accuracy and clinical feasibility. Persistent BD-HC overlap remains a challenge, highlighting the need for larger BD cohorts and complementary multimodal assessments.
