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Updated: Jun 16, 2026

Simultaneous Scalp Electroencephalography (EEG), Electromyography (EMG), and Whole-body Segmental Inertial Recording for Multi-modal Neural Decoding
Published on: July 26, 2013
Integrating memory-guided saccades and EEG for MCI screening: a multimodal LASSO modeling approach
Xinying Zhao1, Fuda Yu1, Hui Wang1
1Department of Neurology, Shijiazhuang People's Hospital, Shijiazhuang, China.
Background:
We investigated differences in memory-guided saccades (MGS) and electroencephalographic (EEG) spectral ratios between cognitively normal older adults and patients with mild cognitive impairment (MCI). A multimodal predictive model was developed to evaluate its potential for early MCI identification.
Methods:
We enrolled 60 participants (37 MCI, 23 controls) who underwent cognitive assessments, 32-channel resting-state EEG, and MGS testing. EEG spectral ratios, including the Delta-to-Alpha Ratio (DAR), Theta-to-Alpha Ratio (TAR), and (Delta+Theta)/(Alpha+Beta) Ratio (DTABR), were extracted along with MGS parameters (latency, accuracy, gain). To prevent data leakage, 21 multimodal features were evaluated using a zero-leakage least absolute shrinkage and selection operator (LASSO) pipeline. A multivariable predictive model was subsequently constructed using Firth's penalized logistic regression, explicitly adjusting for demographic covariates, and internally validated with 1,000 bootstrap resamples.
Results:
MCI patients exhibited significantly prolonged bilateral saccadic latencies, decreased accuracy, and widespread cortical spectral slowing (elevated DAR, TAR, and DTABR across all regions) (all P < 0.05). The LASSO model identified a seven-feature cross-modal diagnostic panel. Following Firth's penalization, rightward saccadic accuracy maintained its significance as an independent protective factor. The combined nomogram achieved an apparent AUC of 0.994 and a bootstrap optimism-corrected AUC of 0.975, demonstrating favorable calibration and promising net clinical benefit.
Conclusion:
MCI patients demonstrate coupled oculomotor and electrophysiological abnormalities, reflecting impaired frontoparietal-sensorimotor network efficiency. Our rigorously penalized multimodal model yields robust internal diagnostic performance, providing a promising exploratory proof-of-concept for the early screening of "cognitive-motor decoupling" in clinical neurology, though large-scale external validation is warranted.

