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Diagnostic accuracy study of EEG network measures for epilepsy versus functional seizures.

Diagnostic accuracy study of EEG network measures for epilepsy versus functional seizures.
Photo by Joshua Chehov / Unsplash
Key Takeaway
Consider that EEG network measures show modest discrimination between epilepsy and functional seizures, but require validation.

This is a diagnostic accuracy study assessing the ability of multivariate resting-state EEG network measures in the 6-9 Hz range to discriminate between non-lesional epilepsy and functional/dissociative seizures (FDS) in a sample of 148 age- and sex-matched individuals (n=75 with epilepsy, n=73 with FDS).

The authors report that the maximum balanced accuracy for discrimination was 67.5%, which was significantly above chance. Sensitivity to epilepsy was 81.8%, while sensitivity to FDS was 53.3%. Classification accuracy improved from 62.6% to 67.5% with epoch-wise averaging, and 77.5% of individuals received a consistent diagnostic label from the top models.

Key limitations noted by the authors include that the dataset was previously examined in a published study, model choice strongly determines classification accuracy, and dimensionality reduction did not provide a significant advantage. The study is based on a single dataset with specific EEG features, and generalizability is not reported.

The authors suggest these measures may support post-test probability estimation in clinic for discriminating epilepsy from FDS. However, the results are preliminary and require replication in independent cohorts before clinical implementation.

Study Details

Sample sizen = 75
EvidenceLevel 5
PublishedApr 2026
View Original Abstract ↓
Background: Distinguishing epilepsy from functional/dissociative seizures (FDS) is an ongoing diagnostic challenge. Misdiagnosis delays appropriate treatment and puts patients at significant risk. Quantitative analyses of clinical EEG offer a potential avenue for developing decision-support tools in the diagnosis of seizure disorders. Recent work using univariate features demonstrated that reliably identifying diagnostic traits in the presence of confounding factors remains challenging. However, diagnostic information might be available in multivariate features such as network-based measures. Using a well-controlled dataset, we run the first diagnostic accuracy study assessing the potential of multivariate resting-state EEG markers to directly discriminate between a diagnosis of epilepsy and one of FDS at the time when a diagnosis is suspected and prior to treatment initiation. Methods: The dataset, previously examined in a published study, includes 148 age- and sex-matched individuals with suspected seizure disorders who were later diagnosed with non-lesional epilepsy (n=75) or FDS (n=73). Eyes-closed, resting-state EEG data used for the analyses were normal on visual inspection, and acquired while participants were medication-free. Functional network measures in the 6-9 Hz range were extracted and machine learning implemented to assess their predictive potential; different model configurations (including varying model types, dimensionality reduction methods, and approaches to enhance feature stability) were tested to identify the most promising approach for future translational implementations. Results: Network measures derived from resting-state EEG discriminate between conditions at levels significantly above chance (maximum balanced accuracy: 67.5%). Their sensitivity to epilepsy (81.8%) is consistently higher than their sensitivity to FDS (53.3%). A systematic assessment of model choices indicates that improving the temporal stability of network features through epoch-wise averaging improves classification accuracy (62.6% to 67.5%). Multiple nonlinear model types succeed on the classification problem, with the three-best performing assigning a consistent diagnostic label to 77.5% of the individuals; however, model choice remains a strong determinant of overall classification accuracy. Dimensionality reduction did not provide a significant advantage in our models. Conclusion: We establish evidence for the clinical validity of selected network-based markers to discriminate between a diagnosis of non-lesional epilepsy and FDS prior to treatment initiation, highlighting the measures potential to support post-test probability estimation in the clinic. Our models, configured to optimise balanced accuracy, classified people with epilepsy more accurately than people with FDS, indicating that these measures are specific to epilepsy and should not be interpreted as markers of a positive diagnosis of FDS.
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