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Epilepsy control with carbamazepine monotherapy from a genetic perspective

BACKGROUND: Ethnicity variation is one of the main factors that may affect drug response in clinical practice. As MTHFR gene affects different transcriptome and proteome which affect the clinical response of drugs. Purpose of the current study was to observe possible variations in plasma levels of c...

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Autores principales: Ullah, Shakir, Ali, Niaz, Khan, Adnan, Ali, Saad, Nazish, Haleema Rehna, Uddin, Zia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238399/
https://www.ncbi.nlm.nih.gov/pubmed/30442198
http://dx.doi.org/10.1186/s40360-018-0261-y
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author Ullah, Shakir
Ali, Niaz
Khan, Adnan
Ali, Saad
Nazish, Haleema Rehna
Uddin, Zia
author_facet Ullah, Shakir
Ali, Niaz
Khan, Adnan
Ali, Saad
Nazish, Haleema Rehna
Uddin, Zia
author_sort Ullah, Shakir
collection PubMed
description BACKGROUND: Ethnicity variation is one of the main factors that may affect drug response in clinical practice. As MTHFR gene affects different transcriptome and proteome which affect the clinical response of drugs. Purpose of the current study was to observe possible variations in plasma levels of carbamazepine monotherapy and seizures’ control in Pakhtun population of Khyber Pakhtunkhwa (KP) in the context of MTHFR (C677T and A1298C) gene polymorphisms. METHODS: Blood was collected from the epileptic patients treated with carbamazepine monotherapy for the first time following respective oral doses on its steady state concentration after 3 h of morning dose at 3(rd) and 6(th) month of the therapy. Plasma carbamazepine levels were determined using reverse phase high performance liquid chromatography after method validation. MTHFR (C677T, AA298C) gene was genotyped. Patients were followed on 3(rd) and 6(th) month of the therapy for monitoring of response to carbamazepine therapy. RESULTS: Following for 3(rd) and 6(th) month of duration of carbamazepine therapy, poor seizure controlled patients were more likely noticed in heterozygous variants (677CT and 1298 AC) of MTHFR gene (P < 0.05). There was no significant (P > 0.05) difference in the dose and plasma level of carbamazepine among different genotypes of MTHFR (C677T and A1298C) gene. Similarly, the difference in dose and plasma level of carbamazepine was not significant (P > 0.05) in the responder and non-responder people with epilepsy. CONCLUSION: Our study suggests that heterozygous variants of MTHFR (C677T and A1298C) gene are associated with poor seizure control in Pakhtun population of KP despite the fact that plasma level of carbamazepine were found within the therapeutic range.
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spelling pubmed-62383992018-11-26 Epilepsy control with carbamazepine monotherapy from a genetic perspective Ullah, Shakir Ali, Niaz Khan, Adnan Ali, Saad Nazish, Haleema Rehna Uddin, Zia BMC Pharmacol Toxicol Research Article BACKGROUND: Ethnicity variation is one of the main factors that may affect drug response in clinical practice. As MTHFR gene affects different transcriptome and proteome which affect the clinical response of drugs. Purpose of the current study was to observe possible variations in plasma levels of carbamazepine monotherapy and seizures’ control in Pakhtun population of Khyber Pakhtunkhwa (KP) in the context of MTHFR (C677T and A1298C) gene polymorphisms. METHODS: Blood was collected from the epileptic patients treated with carbamazepine monotherapy for the first time following respective oral doses on its steady state concentration after 3 h of morning dose at 3(rd) and 6(th) month of the therapy. Plasma carbamazepine levels were determined using reverse phase high performance liquid chromatography after method validation. MTHFR (C677T, AA298C) gene was genotyped. Patients were followed on 3(rd) and 6(th) month of the therapy for monitoring of response to carbamazepine therapy. RESULTS: Following for 3(rd) and 6(th) month of duration of carbamazepine therapy, poor seizure controlled patients were more likely noticed in heterozygous variants (677CT and 1298 AC) of MTHFR gene (P < 0.05). There was no significant (P > 0.05) difference in the dose and plasma level of carbamazepine among different genotypes of MTHFR (C677T and A1298C) gene. Similarly, the difference in dose and plasma level of carbamazepine was not significant (P > 0.05) in the responder and non-responder people with epilepsy. CONCLUSION: Our study suggests that heterozygous variants of MTHFR (C677T and A1298C) gene are associated with poor seizure control in Pakhtun population of KP despite the fact that plasma level of carbamazepine were found within the therapeutic range. BioMed Central 2018-11-15 /pmc/articles/PMC6238399/ /pubmed/30442198 http://dx.doi.org/10.1186/s40360-018-0261-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ullah, Shakir
Ali, Niaz
Khan, Adnan
Ali, Saad
Nazish, Haleema Rehna
Uddin, Zia
Epilepsy control with carbamazepine monotherapy from a genetic perspective
title Epilepsy control with carbamazepine monotherapy from a genetic perspective
title_full Epilepsy control with carbamazepine monotherapy from a genetic perspective
title_fullStr Epilepsy control with carbamazepine monotherapy from a genetic perspective
title_full_unstemmed Epilepsy control with carbamazepine monotherapy from a genetic perspective
title_short Epilepsy control with carbamazepine monotherapy from a genetic perspective
title_sort epilepsy control with carbamazepine monotherapy from a genetic perspective
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238399/
https://www.ncbi.nlm.nih.gov/pubmed/30442198
http://dx.doi.org/10.1186/s40360-018-0261-y
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