Evidence map›Paper›PMID 42536693›Full record

ArticlePloS one2026

Deep learning architectures for EEG-based classification of Dravet syndrome: A comparative study of pre-trained and non-pretrained hybrid CNN-LSTM models.

Sikandar Hussain, Soyiba Jawed, Ali Mir, Mona Ibrahim Ali, Raidah Al-Baradie, Norah Alaqili, Eman Mohammed Nassim Ali, Shahid Bashir

Abstract readComparative Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Sikandar HussainDepartment of Computer and Software Engineering, College of Electrical and Mechanical Engineering, National University of Sciences and Technology(NUST), Islamabad, Pakistan.
Soyiba JawedDepartment of Computer and Software Engineering, College of Electrical and Mechanical Engineering, National University of Sciences and Technology(NUST), Islamabad, Pakistan.ORCID https://orcid.org/0000-0002-9984-3889
Ali MirDepartment of Pediatric Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Mona Ibrahim AliDepartment of Pediatric Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Raidah Al-BaradieDepartment of Pediatric Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Norah AlaqiliDepartment of Pediatric Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Eman Mohammed Nassim AliDepartment of Adult Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
Shahid BashirResearch Center, King Fahad Specialist Hospital Dammam, Dammam, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study explores the potential of artificial intelligence (AI) using a hybrid deep learning Convolutional Neural Network-Long Short-Term Memory (CNN-LSTM) framework, for EEG-based classification and analysis of Dravet Syndrome (DS).

methodThe study cohort comprised nine pediatric patients with DS, confirmed through either a heterozygous pathogenic mutation in the SCN1A gene or a clinical diagnosis consistent with established diagnostic criteria. In addition, EEG recordings from age-matched healthy control subjects and pediatric patients with non-Dravet epilepsy ("abnormal" EEG) were included. Data on demographic information, seizure characteristics, developmental skills, cognitive functions, and genetic results were gathered from patient records. EEG recordings were analyzed using a subject-independent leave-one-subject-out validation strategy, spatial and temporal features by employing this model on preprocessed EEG data, effectively differentiating DS patients from Abnormal cases and healthy controls.

resultAmong the evaluated CNN-LSTM models, the pre-trained architecture achieved superior performance with improved stability across most subjects, with an overall accuracy of 85%, balanced accuracy of 85%, a macro-averaged F1-score of 0.85, and a macro-averaged ROC-AUC of 0.87, demonstrating stable performance for multi-class EEG classification of DS, Abnormal, and control subjects. The non-pretrained model showed reduced sensitivity and increased inter-class confusion, particularly for DS and Abnormal classes.

conclusionThis study demonstrates that a pre-trained CNN-LSTM framework can support automated EEG-based classification of DS-related patterns as a proof-of-concept methodological approach, even in the context of limited subject availability. EEG-specific pretraining improves classification consistency and feature separability compared with training from scratch, highlighting the value of representation learning for rare epilepsy syndromes. Larger multi-center datasets and prospective validation will be required to assess robustness, generalizability, and clinical utility.

Indexed as

Deep LearningElectroencephalographyEpilepsies, MyoclonicCase-Control StudiesChildChild, PreschoolConvolutional Neural NetworksFemaleHumansLong Short Term MemoryMaleNAV1.1 Voltage-Gated Sodium ChannelNAV1.1 Voltage-Gated Sodium ChannelSCN1A protein, human

Identifiers

PMID42536693
PMCPMC13426933

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