吡仑帕奈
癫痫
医学
队列
儿科
抗药性癫痫
内科学
谷氨酸受体
麻醉
受体
精神科
作者
Andreea Nissenkorn,Gerhard Kluger,Susanne Schubert‐Bast,Allan Bayat,Marya Bobylova,Paolo Bonanni,Berten Ceulemans,Antonietta Coppola,Carlo Di Bonaventura,Martha Feucht,Anne Fuchs,Gudrun Gröppel,Gali Heimer,Brigitte Herdt,С.Л. Куликова,К. Yu. Mukhin,Stefania Nicassio,Alessandro Orsini,Maria Panagiotou,Milka Pringsheim,Burkhard Puest,О. А. Пылаева,Georgia Ramantani,Μαρία Τσεκούρα,Paola Ricciardelli,T. Sagie,B. Stark,Pasquale Striano,Andreas van Baalen,Matthias De Wachter,Emanuele Cerulli Irelli,Claudia Cuccurullo,Celina von Stülpnagel,Angelo Russo
出处
期刊:Epilepsia
[Wiley]
日期:2023-02-20
卷期号:64 (4): 866-874
被引量:5
摘要
Abstract Objective Perampanel, an antiseizure drug with α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid receptor antagonist properties, may have a targeted effect in genetic epilepsies with overwhelming glutamate receptor activation. Epilepsies with loss of γ‐aminobutyric acid inhibition (e.g., SCN1A ), overactive excitatory neurons (e.g., SCN2A , SCN8A ), and variants in glutamate receptors (e.g., GRIN2A ) hold special interest. We aimed to collect data from a large rare genetic epilepsy cohort treated with perampanel, to detect possible subgroups with high efficacy. Methods This multicenter project was based on the framework of NETRE (Network for Therapy in Rare Epilepsies), a web of pediatric neurologists treating rare epilepsies. Retrospective data from patients with genetic epilepsies treated with perampanel were collected. Outcome measures were responder rate (50% seizure reduction), and percentage of seizure reduction after 3 months of treatment. Subgroups of etiologies with high efficacy were identified. Results A total of 137 patients with 79 different etiologies, aged 2 months to 61 years (mean = 15.48 ± 9.9 years), were enrolled. The mean dosage was 6.45 ± 2.47 mg, and treatment period was 2.0 ± 1.78 years (1.5 months–8 years). Sixty‐two patients (44.9%) were treated for >2 years. Ninety‐eight patients (71%) were responders, and 93 (67.4%) chose to continue therapy. The mean reduction in seizure frequency was 56.61% ± 34.36%. Sixty patients (43.5%) sustained >75% reduction in seizure frequency, including 38 (27.5%) with >90% reduction in seizure frequency. The following genes showed high treatment efficacy: SCN1A, GNAO1, PIGA, PCDH19, SYNGAP1, POLG1, POLG2 , and NEU1 . Eleven of 17 (64.7%) patients with Dravet syndrome due to an SCN1A pathogenic variant were responders to perampanel treatment; 35.3% of them had >90% seizure reduction. Other etiologies remarkable for >90% reduction in seizures were GNAO1 and PIGA . Fourteen patients had a continuous spike and wave during sleep electroencephalographic pattern, and in six subjects perampanel reduced epileptiform activity. Significance Perampanel demonstrated high safety and efficacy in patients with rare genetic epilepsies, especially in SCN1A, GNAO1, PIGA, PCDH19, SYNGAP1, CDKL5, NEU1 , and POLG , suggesting a targeted effect related to glutamate transmission.