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Evaluation of long-term neurocognitive functions in patients with epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)/epileptic encephalopathy with spike-and-wave activation in sleep (EE-SWAS) - 22/06/23

Doi : 10.1016/j.neucli.2023.102861 
Gunes Sager a, , Gulnur Takis b, Zeynep Vatansever Pinar c, Hanife Duzkalir d, Ayberk Turkyilmaz e, Yakup Çağ f, Yasemin Akin f
a Department of Pediatric Neurology, University of Health Sciences, Kartal Dr. LutfiKirdar City Hospital, Istanbul, Turkey 
b Specialized Psychologist, Medeniyet University, Istanbul, Turkey 
c Department of Child and Adolescent Psychiatry, University of Health Sciences, Kartal Dr. LutfiKirdar City Hospital, Istanbul, Turkey 
d Department of Radiology, University of Health Sciences, Kartal Dr. LutfiKirdar City Hospital, Istanbul, Turkey 
e Department of Medical Genetics, KaradenizTechical University Faculty of Medicine, Trabzon, Turkey 
f Department of Pediatrics, University of Health Sciences, Kartal Dr. LutfiKirdar City Hospital, Istanbul, Turkey 

Corresponding author at: Department of Pediatric Neurology, Kartal Dr. LutfiKirdar City Hospital, SemsiDenizer Avenue, Cevizli, 34890, Kartal, Istanbul, Turkey.Department of Pediatric NeurologyKartal Dr. LutfiKirdar City Hospital, SemsiDenizer AvenueCevizli, 34890, KartalIstanbulTurkey

Abstract

Objectives

Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS) or the newly named Epileptic encephalopathy with spike-and-wave activation in sleep (EE-SWAS) is a syndrome in which epileptiform abnormalities are associated with the progressive impairment of cognitive functions. This study aimed to evaluate the neurocognitive executive functions of patients at later ages and determine the long-term prognosis of the condition, as well as the factors affecting this.

Methods

This is a hospital-based cross-sectional study of 17 patients with a diagnosis of CSWS, and a minimum age of 7.5 years. The Wechsler Intelligence Scale for Children-Fourth Edition (WISC-IV) was used for neurocognitive assessment. The use of immunotherapy (intravenous immunoglobulin and/or steroid for at least 6 months) at the time of initial diagnosis, baseline activity and spike wave index (SWI) of the last wake and sleep EEG, cranial MRI findings, active epileptic seizures since the last examination, and WISC-IV parameters were statistically compared. The results of patients with genetic etiology determined by the whole exome sequencing (WES) method are also reported.

Results

A total of 17 patients were included in the study, with a mean age of 10.30 ± 3.15 years (range from 7.9 to 15.8 years). The mean full scale IQ score of the subjects was 61.41 ± 17.81 (range 39–91), classified as follows: 5.9% (n = 1), average; 23.5% (n = 4), low average; 5.9% (n = 1), very low; 35.3% (n = 6), extremely low (upper range); 29.4% (n = 5), extremely low (lower range) intelligence. Among the four domains of WISC-IV, the most affected index was the Working Memory Index (WMI). EEG parameters, cranial MRI findings and treatment with immunotherapy did not have a significant effect on neurocognitive outcomes. Thirteen patients (76%) were evaluated with WES for a genetic etiology. Pathogenic variants in 5 different genes (GRIN2A, SLC12A5, SCN1A, SCN8A, ADGRV1) associated with epilepsy were detected in 5/13 patients (38%).

Conclusion

These results indicated that neurocognition is highly affected in the long term in CSWS.

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Keywords : Children, Epilepsy, Neurocognition, Slow-wave sleep, Status epilepticus, Wechsler Intelligence Scale


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Vol 53 - N° 1

Article 102861- février 2023 Retour au numéro
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