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MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study

OBJECTIVE: Our study aimed to evaluate the influence of methylenetetrahydrofolate reductase (MTHFR) polymorphism on the clinical features and therapeutic effects in patients with migraine. METHODS: The data of 135 patients with migraine were collected from January 2021 to December 2021. The MTHFR C6...

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Autores principales: Guo, Jianhao, Hao, Xing, Wang, Rongrong, Lian, Ke, Jiang, Jun, Chen, Na, Feng, Zhiying, Rao, Yuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816401/
https://www.ncbi.nlm.nih.gov/pubmed/36619923
http://dx.doi.org/10.3389/fneur.2022.1074857
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author Guo, Jianhao
Hao, Xing
Wang, Rongrong
Lian, Ke
Jiang, Jun
Chen, Na
Feng, Zhiying
Rao, Yuefeng
author_facet Guo, Jianhao
Hao, Xing
Wang, Rongrong
Lian, Ke
Jiang, Jun
Chen, Na
Feng, Zhiying
Rao, Yuefeng
author_sort Guo, Jianhao
collection PubMed
description OBJECTIVE: Our study aimed to evaluate the influence of methylenetetrahydrofolate reductase (MTHFR) polymorphism on the clinical features and therapeutic effects in patients with migraine. METHODS: The data of 135 patients with migraine were collected from January 2021 to December 2021. The MTHFR C677T polymorphism was analyzed. The pain intensity was evaluated using a numerical rating scale (NRS) during treatment. The levels of folic acid, homocysteine (Hcy), vitamin B12, interleukin-2 (IL-2), IL-4, and ferritin, and changes of NRS were compared between folic acid and conventional treatment groups stratified by different genotypes of MTHFR in migraine patients. RESULTS: The levels of Hcy and ferritin in male patients were higher than that in female patients (P < 0.05); Compared with CC and CT genotype groups, the TT genotype group showed significantly higher Hcy levels (P < 0.05) and lower folic acid levels (P < 0.05); In both folic acid and conventional treatment groups, a significant decrease in NRS score was observed in different genotypes post-treatment (P < 0.05). Patients with TT genotype in the folic acid treatment group showed better therapeutic efficacy than conventional treatment group (P < 0.05). There is no significant difference in the therapeutic efficacy in other genotypes between the two groups (P > 0.05). CONCLUSION: The MTHFR C677T genotyping may provide a new method to guide and optimize individualized medication for migraine patients.
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spelling pubmed-98164012023-01-07 MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study Guo, Jianhao Hao, Xing Wang, Rongrong Lian, Ke Jiang, Jun Chen, Na Feng, Zhiying Rao, Yuefeng Front Neurol Neurology OBJECTIVE: Our study aimed to evaluate the influence of methylenetetrahydrofolate reductase (MTHFR) polymorphism on the clinical features and therapeutic effects in patients with migraine. METHODS: The data of 135 patients with migraine were collected from January 2021 to December 2021. The MTHFR C677T polymorphism was analyzed. The pain intensity was evaluated using a numerical rating scale (NRS) during treatment. The levels of folic acid, homocysteine (Hcy), vitamin B12, interleukin-2 (IL-2), IL-4, and ferritin, and changes of NRS were compared between folic acid and conventional treatment groups stratified by different genotypes of MTHFR in migraine patients. RESULTS: The levels of Hcy and ferritin in male patients were higher than that in female patients (P < 0.05); Compared with CC and CT genotype groups, the TT genotype group showed significantly higher Hcy levels (P < 0.05) and lower folic acid levels (P < 0.05); In both folic acid and conventional treatment groups, a significant decrease in NRS score was observed in different genotypes post-treatment (P < 0.05). Patients with TT genotype in the folic acid treatment group showed better therapeutic efficacy than conventional treatment group (P < 0.05). There is no significant difference in the therapeutic efficacy in other genotypes between the two groups (P > 0.05). CONCLUSION: The MTHFR C677T genotyping may provide a new method to guide and optimize individualized medication for migraine patients. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816401/ /pubmed/36619923 http://dx.doi.org/10.3389/fneur.2022.1074857 Text en Copyright © 2022 Guo, Hao, Wang, Lian, Jiang, Chen, Feng and Rao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Guo, Jianhao
Hao, Xing
Wang, Rongrong
Lian, Ke
Jiang, Jun
Chen, Na
Feng, Zhiying
Rao, Yuefeng
MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title_full MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title_fullStr MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title_full_unstemmed MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title_short MTHFR polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: An observational study
title_sort mthfr polymorphism's influence on the clinical features and therapeutic effects in patients with migraine: an observational study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816401/
https://www.ncbi.nlm.nih.gov/pubmed/36619923
http://dx.doi.org/10.3389/fneur.2022.1074857
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