» Articles » PMID: 39658609

Effects of CYP2C19 and CYP2C9 Polymorphisms on the Efficacy and Plasma Concentration of Lacosamide in Pediatric Patients with Epilepsy in China

Overview
Journal Eur J Pediatr
Specialty Pediatrics
Date 2024 Dec 10
PMID 39658609
Authors
Affiliations
Soon will be listed here.
Abstract

Conclusion: LCM plasma concentrations were strongly associated with its clinical efficacy and toxicity. CYP2C19 polymorphisms affect the plasma concentration and treatment efficacy in pediatric patients with epilepsy. CYP2C19 PMs with two no-function alleles are likely to have higher LCM plasma concentrations.

What Is Known: • LCM is metabolized by CYP2C19, CYP2C9, and CYP3A4 into pharmacologically inactive O-desmethyl-lacosamide; it primarily undergoes renal elimination. • Plasma LCM concentrations in patients treated with the recommended dose vary widely between and within individuals variability.

What Is New: • CYP2C19 polymorphisms affect the plasma concentration and treatment efficacy in Chinese pediatric patients with epilepsy. • CYP2C19 PMs with two no-function alleles are likely to have higher plasma LCM concentrations.

References
1.
Moshe S, Perucca E, Ryvlin P, Tomson T . Epilepsy: new advances. Lancet. 2014; 385(9971):884-98. DOI: 10.1016/S0140-6736(14)60456-6. View

2.
Vossler D, Knake S, OBrien T, Watanabe M, Brock M, Steiniger-Brach B . Efficacy and safety of adjunctive lacosamide in the treatment of primary generalised tonic-clonic seizures: a double-blind, randomised, placebo-controlled trial. J Neurol Neurosurg Psychiatry. 2020; 91(10):1067-1075. PMC: 7509528. DOI: 10.1136/jnnp-2020-323524. View

3.
Arabi M, Alsaadi T, Nasreddine W, Al-Hashel J, Dirani M, Beydoun A . Efficacy and tolerability of treatment with lacosamide: Postmarketing experience from the Middle East region. Epilepsy Behav. 2018; 84:118-121. DOI: 10.1016/j.yebeh.2018.04.020. View

4.
Biton V, Gil-Nagel A, Isojarvi J, Doty P, Hebert D, Fountain N . Safety and tolerability of lacosamide as adjunctive therapy for adults with partial-onset seizures: Analysis of data pooled from three randomized, double-blind, placebo-controlled clinical trials. Epilepsy Behav. 2015; 52(Pt A):119-27. DOI: 10.1016/j.yebeh.2015.09.006. View

5.
Zadeh W, Escartin A, Byrnes W, Tennigkeit F, Borghs S, Li T . Efficacy and safety of lacosamide as first add-on or later adjunctive treatment for uncontrolled partial-onset seizures: A multicentre open-label trial. Seizure. 2015; 31:72-9. DOI: 10.1016/j.seizure.2015.07.001. View