Wpływ polimorfizmu genu KCNA3 na skuteczność i stężenie perampenelu w osoczu u pacjentów z opornościową epilepsją
KCNA3 Gene Polymorphism Affects the Efficacy and Plasma Concentration of Perampanel in Patients With Refractory Epilepsy
W skrócie
Badanie wykazało, że odmiana genetyczna KCNA3 rs2821557 wpływa na to, jak dobrze lek perampenel działa u pacjentów z epilepsją oporną na leczenie - osoby z wariantem TT miały lepsze wyniki leczenia. Stężenie leku w krwi było niższe u pacjentów z wariantami CT lub TT w porównaniu z wariantem CC, zwłaszcza u dzieci w wieku 4-14 lat, kobiet i osób z wyższym BMI. Wyniki sugerują, że badanie tej odmiany genetycznej mogłoby pomóc lekarzom przewidzieć, czy perampenel będzie skuteczny dla konkretnego pacjenta i dostosować dawkę leku.
Oryginalny abstract (angielski)
BACKGROUND: Perampanel (PER) is the only third-generation anti-seizure medication targeting AMPA receptors, but its efficacy varies between patients. Whether KCNA3 polymorphisms influence PER response in drug-resistant epilepsy remains unknown. This study aims to evaluate the impact of KCNA3 rs2821557 polymorphisms on PER efficacy and plasma concentrations in patients with refractory epilepsy. METHODS: Blood samples were collected from 119 patients who received PER for at least 3 weeks, in accordance with inclusion and exclusion criteria. KCNA3 rs2821557 genotypes were identified using first-generation Sanger sequencing, and plasma PER concentrations were quantified by ultra-high-performance liquid chromatography to assess associations between the KCNA3 rs2821557 gene polymorphism, PER efficacy, and plasma drug concentrations. RESULTS: The therapeutic efficacy of PER in managing patients with refractory epilepsy was 65.55% (78/119). The proportion of patients with the KCNA3 rs2821557 TT genotype was significantly greater in the effective group than the ineffective group. Plasma PER concentrations in patients with CT or TT genotypes were significantly lower than in those with the CC genotype, a pattern also observed in patients aged 4-14 years, female patients, patients with a body mass index ranging from 18.5 to 24.0 kg/m, and patients with disease duration exceeding 1 year. CONCLUSIONS: The KCNA3 rs2821557 polymorphism is an important predictor of the therapeutic efficacy of PER in controlling epileptic seizures and a determinant of the attainment of therapeutic plasma PER concentrations.