Novel UBE3A pathogenic variant in a large Georgian family produces non-convulsive status epilepticus responsive to ketogenic diet. (January 2022)

• Record Type: Journal Article
• Authors: Melikishvili, Gia; Bienvenu, Thierry; Tabatadze, Nazhi; Gachechiladze, Tamar; Kurua, Ekaterine; Gverdtsiteli, Sopio; Melikishvili, Mariam; Dulac, Olivier
• Is Part Of: Seizure. Volume 94(2022)
• Page Start: 70
• Page End: 73
• Publication Date: 2022-01
• Subjects: NCSE Non-convulsive status epilepticus -- AS Angelman syndrome -- KD Ketogenic diet -- KB Ketone bodies -- GABA Gamma-amino butyrics acid -- EEG Electroencephalogram; Angelman syndrome -- Ketogenic diet -- UBE3A frameshift variant -- Hypsarrhythmia-like pattern; Epilepsy -- Periodicals; Epilepsy -- Periodicals; Seizures -- Periodicals; Épilepsie -- Périodiques; Electronic journals; Electronic journals; 616.853
• DOI: 10.1016/j.seizure.2021.11.012
• Languages: English
• ISSNs: 1059-1311

Abstract

Abstract: Purpose: To report the effect of the ketogenic diet (KD) on non-convulsive status epilepticus (NCSE) due to Angelman syndrome (AS) in two members of a large Georgian family affected by a novel frameshift variant in the UBE3A gene (NM_000462.3). Methods: We evaluated two members of this family who were affected with clinical and EEG features of AS. Clinical history with special emphasis on development, seizure type, frequency, and treatment was reviewed. Routine and long-term video EEG monitoring were conducted, particularly during NCSE. A non-fasting inpatient KD protocol was implemented using blended food orally with full administration of 4:1 (fat to non-fat) ratio. Urine ketone bodies (KBs), measured with urine ketone acetone strips readings, reached 150 mg/dL in both patients. Results: Patients had characteristic signs of AS and presented with epilepsy between the age of 2–4 years. As methylation tests were negative, next generation sequencing disclosed a c.2365del variant. For both, NCSE was revealed by cognitive deterioration and did not respond to anti-seizure medication. As recommended, IV pyridoxine, benzodiazepines, and valproic acid were administered, but without success. For both patients, NCSE resolved on the second-third day of KD initiation, before the appearance of ketonuria and resulting in improved communication, mood and sleep. Conclusion: KD is safe and effective for the treatment of NCSE due to AS. Resolution before the appearance of ketone bodies points to a possible mechanism of action of KD.