Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients

Abstract Background Many antiseizure medications (ASMs) control seizures by blocking voltage-dependent sodium channels. Polymorphisms of sodium channel genes may affect the response to ASMs due to altering the effect of ASMs on blocking sodium channels. Methods We conducted a retrospective study of...

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Main Authors: Chih-Hsiang Lin, Chen-Jui Ho, Yan-Ting Lu, Meng-Han Tsai
Format: Article
Language:English
Published: BMC 2021-09-01
Series:BMC Neurology
Subjects:
Online Access:https://doi.org/10.1186/s12883-021-02395-2
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author Chih-Hsiang Lin
Chen-Jui Ho
Yan-Ting Lu
Meng-Han Tsai
author_facet Chih-Hsiang Lin
Chen-Jui Ho
Yan-Ting Lu
Meng-Han Tsai
author_sort Chih-Hsiang Lin
collection DOAJ
description Abstract Background Many antiseizure medications (ASMs) control seizures by blocking voltage-dependent sodium channels. Polymorphisms of sodium channel genes may affect the response to ASMs due to altering the effect of ASMs on blocking sodium channels. Methods We conducted a retrospective study of epilepsy patients followed up at the Neurological Department of Kaohsiung Chang Gung Memorial Hospital, Taiwan between January 2010 and December 2018. We categorized the patients into response, partial response, and failure to sodium channel blocking ASM groups. Sodium channel blocking ASMs included phenytoin, carbamazepine, lamotrigine, oxcarbazepine, lacosamide, zonisamide, topiramate, and valproic acid. A subgroup of predominant sodium channel blocking ASMs included phenytoin, carbamazepine, lamotrigine, oxcarbazepine, and lacosamide. Associations between the response of ASMs and single-nucleotide polymorphisms of SCN1A, SCN1B, SCN2A, and SCN9A were analyzed. Results Two hundred Taiwanese patients and 21 single-nucleotide polymorphisms among SCN1A, SCN1B, SCN2A, and SCN9A were evaluated. We found allele C of rs55742440 in SCN1B was statistically significantly associated with not achieving seizure-free with sodium channel blocking ASMs. For the predominant sodium channel blocking ASMs group, no SNPs were associated with the response of ASMs. Conclusion Single-nucleotide polymorphism in SCN1B was associated with the response to sodium channel blocking ASMs. This highlights the possibility that beta subunits may affect the function of sodium channels and resulted in different responsiveness to ASMs.
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spelling doaj.art-80a6056fa73941eebe713a07afef64ac2022-12-21T18:57:34ZengBMCBMC Neurology1471-23772021-09-0121111310.1186/s12883-021-02395-2Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patientsChih-Hsiang Lin0Chen-Jui Ho1Yan-Ting Lu2Meng-Han Tsai3Department of Neurology, Kaohsiung Chang Gung Memorial Hospital, Colleague of Medicine, Chang Gung UniversityDepartment of Neurology, Kaohsiung Chang Gung Memorial Hospital, Colleague of Medicine, Chang Gung UniversityDepartment of Neurology, Kaohsiung Chang Gung Memorial Hospital, Colleague of Medicine, Chang Gung UniversityDepartment of Neurology, Kaohsiung Chang Gung Memorial Hospital, Colleague of Medicine, Chang Gung UniversityAbstract Background Many antiseizure medications (ASMs) control seizures by blocking voltage-dependent sodium channels. Polymorphisms of sodium channel genes may affect the response to ASMs due to altering the effect of ASMs on blocking sodium channels. Methods We conducted a retrospective study of epilepsy patients followed up at the Neurological Department of Kaohsiung Chang Gung Memorial Hospital, Taiwan between January 2010 and December 2018. We categorized the patients into response, partial response, and failure to sodium channel blocking ASM groups. Sodium channel blocking ASMs included phenytoin, carbamazepine, lamotrigine, oxcarbazepine, lacosamide, zonisamide, topiramate, and valproic acid. A subgroup of predominant sodium channel blocking ASMs included phenytoin, carbamazepine, lamotrigine, oxcarbazepine, and lacosamide. Associations between the response of ASMs and single-nucleotide polymorphisms of SCN1A, SCN1B, SCN2A, and SCN9A were analyzed. Results Two hundred Taiwanese patients and 21 single-nucleotide polymorphisms among SCN1A, SCN1B, SCN2A, and SCN9A were evaluated. We found allele C of rs55742440 in SCN1B was statistically significantly associated with not achieving seizure-free with sodium channel blocking ASMs. For the predominant sodium channel blocking ASMs group, no SNPs were associated with the response of ASMs. Conclusion Single-nucleotide polymorphism in SCN1B was associated with the response to sodium channel blocking ASMs. This highlights the possibility that beta subunits may affect the function of sodium channels and resulted in different responsiveness to ASMs.https://doi.org/10.1186/s12883-021-02395-2Antiseizure medicationsSodium channel geneSingle-nucleotide polymorphismsDrug resistance epilepsySCN1B
spellingShingle Chih-Hsiang Lin
Chen-Jui Ho
Yan-Ting Lu
Meng-Han Tsai
Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
BMC Neurology
Antiseizure medications
Sodium channel gene
Single-nucleotide polymorphisms
Drug resistance epilepsy
SCN1B
title Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
title_full Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
title_fullStr Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
title_full_unstemmed Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
title_short Response to Sodium Channel blocking Antiseizure medications and coding polymorphisms of Sodium Channel genes in Taiwanese epilepsy patients
title_sort response to sodium channel blocking antiseizure medications and coding polymorphisms of sodium channel genes in taiwanese epilepsy patients
topic Antiseizure medications
Sodium channel gene
Single-nucleotide polymorphisms
Drug resistance epilepsy
SCN1B
url https://doi.org/10.1186/s12883-021-02395-2
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