Investigating the Effect of Cognitive Rehabilitation on Cognitive Impairment Associated With Antiseizure Medications in Patients With Epilepsy


Karadaş A. Ö., Shafiyev J., KARADAŞ Ö., Karadaş Ç., Şimşek U. B., Özenç B., ...Daha Fazla

Clinical EEG and Neuroscience, cilt.57, sa.3, ss.285-292, 2026 (SCI-Expanded, Scopus)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 57 Sayı: 3
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1177/15500594251376071
  • Dergi Adı: Clinical EEG and Neuroscience
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE, Health Research Premium Collection (ProQuest), Pharma Collection (ProQuest)
  • Sayfa Sayıları: ss.285-292
  • Anahtar Kelimeler: cognitive rehabilitation, antiseizure medications, P300, N200, MoCA
  • Sağlık Bilimleri Üniversitesi Adresli: Evet

Özet

Objective Most existing studies on cognitive rehabilitation in epilepsy focus on patients undergoing epilepsy surgery or classify interventions based on epilepsy type. This study aimed to determine whether antiseizure medications (ASMs) cause cognitive dysfunction in epilepsy patients by using neuropsychological assessments and auditory event-related potentials (ERPs), and whether cognitive rehabilitation can reduce this potential impact. Materials and Methods The study included patients scheduled to begin ASM monotherapy. All participants first underwent a face-to-face Montreal Cognitive Assessment (MoCA). Auditory ERPs including P300 and N200 latencies, and N2 to P3 peak-to-peak amplitudes were recorded in the electrophysiology laboratory. Patients were randomly divided into two groups: Group A (no cognitive rehabilitation) and Group B (received cognitive rehabilitation). After two months, both MoCA and auditory ERP measurements were repeated, and the results were statistically analyzed. Results In Group A, patients using carbamazepine (CBZ), zonisamide (ZNS), or valproic acid (VPA) showed a statistically significant decline in MoCA scores and auditory ERP results (P < .05), suggesting a protective role of rehabilitation. For topiramate (TPM), cognitive decline was weakly significant even with rehabilitation (P = .031)