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Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs
Background: Migraine is a multifactorial neurological disorder characterized by frequent moderate to severe intensity headaches. The genetic variations in synaptic and post-receptor signalling proteins have direct effect on the process of serotonergic neurotransmission. Methods: We aimed to investig...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444595/ https://www.ncbi.nlm.nih.gov/pubmed/38011351 http://dx.doi.org/10.18502/cjn.v22i1.12616 |
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author | Kesavan, Pallavi Satheesh, Aiswarya Padmaja Rasheed, Akram Husain Rehman Syed Veerappan, Umamaheshwari Kannaian, Subramaniyan Veerabathiran, Ramakrishnan |
author_facet | Kesavan, Pallavi Satheesh, Aiswarya Padmaja Rasheed, Akram Husain Rehman Syed Veerappan, Umamaheshwari Kannaian, Subramaniyan Veerabathiran, Ramakrishnan |
author_sort | Kesavan, Pallavi |
collection | PubMed |
description | Background: Migraine is a multifactorial neurological disorder characterized by frequent moderate to severe intensity headaches. The genetic variations in synaptic and post-receptor signalling proteins have direct effect on the process of serotonergic neurotransmission. Methods: We aimed to investigate the genetic association of serotonin transporter (SERT) 5-hydroxytryptamine transporter-linked promoter region (5-HTTLPR) polymorphism and migraine risk in South-Indian population. A total of 304 subjects with migraine including with aura (MA) and without aura (MO) and 308 controls were included in the present study. The single nucleotide polymorphism (SNP) was detected using polymerase chain reaction (PCR) and confirmed by deoxyribonucleic acid (DNA) sequencing. Results: The genotyping analysis revealed insignificant relationship with migraine subjects when compared with controls (P > 0.05). The minor ‘S’ allele showed no association with odds ratio (OR) = 1.23 [95% confidence interval (CI): 0.90-1.66], heterozygote with OR = 1.18 (95% CI: 0.82-1.69), and homozygote with OR = 1.51 (95% CI: 0.52-4.35). Conclusion: Further clinical studies are required to validate the results of SERT 5-HTTLPR promoter polymorphism in diverse ethnic descents especially in Asian populations. |
format | Online Article Text |
id | pubmed-10444595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-104445952023-08-24 Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs Kesavan, Pallavi Satheesh, Aiswarya Padmaja Rasheed, Akram Husain Rehman Syed Veerappan, Umamaheshwari Kannaian, Subramaniyan Veerabathiran, Ramakrishnan Curr J Neurol Original Article Background: Migraine is a multifactorial neurological disorder characterized by frequent moderate to severe intensity headaches. The genetic variations in synaptic and post-receptor signalling proteins have direct effect on the process of serotonergic neurotransmission. Methods: We aimed to investigate the genetic association of serotonin transporter (SERT) 5-hydroxytryptamine transporter-linked promoter region (5-HTTLPR) polymorphism and migraine risk in South-Indian population. A total of 304 subjects with migraine including with aura (MA) and without aura (MO) and 308 controls were included in the present study. The single nucleotide polymorphism (SNP) was detected using polymerase chain reaction (PCR) and confirmed by deoxyribonucleic acid (DNA) sequencing. Results: The genotyping analysis revealed insignificant relationship with migraine subjects when compared with controls (P > 0.05). The minor ‘S’ allele showed no association with odds ratio (OR) = 1.23 [95% confidence interval (CI): 0.90-1.66], heterozygote with OR = 1.18 (95% CI: 0.82-1.69), and homozygote with OR = 1.51 (95% CI: 0.52-4.35). Conclusion: Further clinical studies are required to validate the results of SERT 5-HTTLPR promoter polymorphism in diverse ethnic descents especially in Asian populations. Tehran University of Medical Sciences 2023-01-05 /pmc/articles/PMC10444595/ /pubmed/38011351 http://dx.doi.org/10.18502/cjn.v22i1.12616 Text en Copyright © 2023 Iranian Neurological Association, and Tehran University of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Kesavan, Pallavi Satheesh, Aiswarya Padmaja Rasheed, Akram Husain Rehman Syed Veerappan, Umamaheshwari Kannaian, Subramaniyan Veerabathiran, Ramakrishnan Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title | Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title_full | Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title_fullStr | Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title_full_unstemmed | Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title_short | Association analysis of serotonin transporter gene polymorphism among the South-Indian migraineurs |
title_sort | association analysis of serotonin transporter gene polymorphism among the south-indian migraineurs |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444595/ https://www.ncbi.nlm.nih.gov/pubmed/38011351 http://dx.doi.org/10.18502/cjn.v22i1.12616 |
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