Characterizing sleep disturbances in developmental and epileptic encephalopathies through natural language processing: A retrospective monocentric study

Abstract Objective Sleep disorders are frequent but undercharacterized comorbidities in developmental and epileptic encephalopathies (DEEs). We aimed to estimate the frequency, spectrum, and burden of sleep disturbances across genetic DEE subtypes using real‐world data extracted from electronic health records (EHRs) through natural language processing (NLP). Methods We conducted a retrospective cohort study using Dr. Warehouse, an NLP‐enabled clinical data warehouse, at a tertiary pediatric center. Data were extracted from January to April 2025. Patients with a group of defined DEEs were identified from narrative clinical notes and matched 1:2 with pediatric neurology patients without history of epilepsy by age, follow‐up duration, and document volume. Predefined sleep‐related terms were extracted from free‐text reports. The proportion of patients with ≥1 documented mention during follow‐up was used to estimate occurrence, alongside multivariable logistic regression analyses and a cumulative sleep burden score. Results The final cohort included 884 patients with DEE and 1280 matched controls. At least one sleep‐related disturbance was documented in 63.7% of DEE patients, significantly higher than in controls. The most frequent terms were “sleep disorder,” “nocturnal seizures,” and “night awakenings.” Marked heterogeneity emerged across DEE subtypes; SYNGAP1 ‐DEE showed the highest frequency of sleep disorders, Lennox–Gastaut syndrome was strongly associated with nocturnal seizures, and KCNT1 ‐ and PCDH19 ‐DEE were more frequently associated with sleep apnea. DEE patients also exhibited a significantly higher cumulative burden of sleep disturbances compared with controls, with Lennox–Gastaut syndrome showing the greatest burden. Significance NLP‐based mining of unstructured EHR data enables large‐scale characterization of sleep disorders in DEEs, revealing DEE subtype‐specific sleep phenotypes. Routine and etiology‐informed assessment of sleep disturbances should be integrated into the clinical management of DEEs.

Authors

Institutions

Publication Details

Journal
Epilepsia
Published
2026-10-12
DOI
https://doi.org/10.1002/epi.70485
Primary Topic
Sleep and related disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Characterizing sleep disturbances in developmental and epileptic encephalopathies through natural language processing: A retrospective monocentric study

Nicole Chémaly, Nicolas Garcelon, Rima Nabbout, Gianluca D’Onofrio et al.
Epilepsia
Sleep and related disorders
article

Characterizing sleep disturbances in developmental and epileptic encephalopathies through natural language processing: A retrospective monocentric study

Nicole Chémaly, Nicolas Garcelon, Rima Nabbout, Gianluca D’Onofrio, Maxime Douillet, Tommaso Lo Barco, Audrey Duval, Xiaoyi Chen
article en

Abstract

Abstract Objective Sleep disorders are frequent but undercharacterized comorbidities in developmental and epileptic encephalopathies (DEEs). We aimed to estimate the frequency, spectrum, and burden of sleep disturbances across genetic DEE subtypes using real‐world data extracted from electronic health records (EHRs) through natural language processing (NLP). Methods We conducted a retrospective cohort study using Dr. Warehouse, an NLP‐enabled clinical data warehouse, at a tertiary pediatric center. Data were extracted from January to April 2025. Patients with a group of defined DEEs were identified from narrative clinical notes and matched 1:2 with pediatric neurology patients without history of epilepsy by age, follow‐up duration, and document volume. Predefined sleep‐related terms were extracted from free‐text reports. The proportion of patients with ≥1 documented mention during follow‐up was used to estimate occurrence, alongside multivariable logistic regression analyses and a cumulative sleep burden score. Results The final cohort included 884 patients with DEE and 1280 matched controls. At least one sleep‐related disturbance was documented in 63.7% of DEE patients, significantly higher than in controls. The most frequent terms were “sleep disorder,” “nocturnal seizures,” and “night awakenings.” Marked heterogeneity emerged across DEE subtypes; SYNGAP1 ‐DEE showed the highest frequency of sleep disorders, Lennox–Gastaut syndrome was strongly associated with nocturnal seizures, and KCNT1 ‐ and PCDH19 ‐DEE were more frequently associated with sleep apnea. DEE patients also exhibited a significantly higher cumulative burden of sleep disturbances compared with controls, with Lennox–Gastaut syndrome showing the greatest burden. Significance NLP‐based mining of unstructured EHR data enables large‐scale characterization of sleep disorders in DEEs, revealing DEE subtype‐specific sleep phenotypes. Routine and etiology‐informed assessment of sleep disturbances should be integrated into the clinical management of DEEs.

Epilepsia
Hôpital Necker-Enfants Malades (FR), University of Minnesota (US), Inserm (FR), Université Paris Cité (FR), Institut des Maladies Génétiques Imagine (FR)
Openalex Percentile: Top 7%
Sleep and related disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.