COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women

Detalhes bibliográficos
Autor(a) principal: Szezerbaty, Stheace Kelly Fernandes
Data de Publicação: 2021
Outros Autores: Zicarelli , Carlos Alexandre Martins, Lima, Luana Oliveira de, Perrucini, Priscila Daniele Oliveira, Fernandes, Karen Barros Parron, Poli-Frederico, Regina Célia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/15225
Resumo: To investigate the influence of the catechol-O-methyltransferase enzyme (COMT) single nucleotide polymorphism (SNP) rs4680 (G/A) on fibromyalgia in women. In this observational study of case-control type 29 women with a diagnosis of FM (cases) and 31 healthy non-fibromyalgia women (controls). Sociodemographic and anthropometric data were collected, as well as data relating to Symptom Severity Scale and Generalized Pain Index and peripheral blood samples for DNA extraction; genotypic analyzes were performed by PCR-SSP. We observed that rs4680 AA genotype was more frequently observed in fibromyalgia than controls (p=0.02). The A allele was also more often present in the fibromyalgia participants than in their control peers (p = 0.03). There was a statistically significant association between race and FM sufferers, showing that those of white ethnicity had a 2.05 times greater chance of developing the syndrome than non-white individuals (p=0.03; CI 95% 0.93 – 4.53). A statistically significant correlation between age and FM was observed (rS=0.812, p=0.01). This study demonstrates that white women above the age of 45, who have the AA genotype or A-allele, presents a higher risk of developing FM, showing that this polymorphism of the COMT gene may be one of the risk factors for the fibromyalgia.
id UNIFEI_4d4b7d91befe186ab23cfc4edc082c53
oai_identifier_str oai:ojs.pkp.sfu.ca:article/15225
network_acronym_str UNIFEI
network_name_str Research, Society and Development
repository_id_str
spelling COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in womenEl polimorfismo de un solo nucleótido rs4680 en el gen COMT, la etnia y la edad se asocian con la fibromialgia en las mujeresPolimorfismo de nucleotídeo único rs4680 no gene COMT, etnia e idade estão associadas com fibromialgia em mulheresFibromyalgiaWomenGenetic PolymorphismPainCatechol-O-methyltransferase.FibromialgiaMujeresPolimorfismo genéticoDolorCatecol-O-metiltransferasa.FibromialgiaMulheresPolimorfismo genéticoDorCatecol-O-metiltransferase.To investigate the influence of the catechol-O-methyltransferase enzyme (COMT) single nucleotide polymorphism (SNP) rs4680 (G/A) on fibromyalgia in women. In this observational study of case-control type 29 women with a diagnosis of FM (cases) and 31 healthy non-fibromyalgia women (controls). Sociodemographic and anthropometric data were collected, as well as data relating to Symptom Severity Scale and Generalized Pain Index and peripheral blood samples for DNA extraction; genotypic analyzes were performed by PCR-SSP. We observed that rs4680 AA genotype was more frequently observed in fibromyalgia than controls (p=0.02). The A allele was also more often present in the fibromyalgia participants than in their control peers (p = 0.03). There was a statistically significant association between race and FM sufferers, showing that those of white ethnicity had a 2.05 times greater chance of developing the syndrome than non-white individuals (p=0.03; CI 95% 0.93 – 4.53). A statistically significant correlation between age and FM was observed (rS=0.812, p=0.01). This study demonstrates that white women above the age of 45, who have the AA genotype or A-allele, presents a higher risk of developing FM, showing that this polymorphism of the COMT gene may be one of the risk factors for the fibromyalgia.Investigar la influencia del polimorfismo de un solo nucleótido (SNP) rs4680 (G / A) de la enzima catecol-O-metiltransferasa (COMT) sobre la fibromialgia en mujeres. En este estudio observacional de casos y controles, 29 mujeres diagnosticadas con FM (casos) y 31 mujeres sanas sin fibromialgia (controles). Se recolectaron datos sociodemográficos y antropométricos, así como datos relacionados con la Escala de Severidad de Síntomas e Índice de Dolor Generalizado y muestras de sangre periférica para extracción de ADN; Los análisis genotípicos se realizaron mediante PCR-SSP. Observamos que el genotipo rs4680 AA se observó con mayor frecuencia en la fibromialgia que en los controles (p = 0,02). El alelo A también estuvo presente con mayor frecuencia en los participantes con fibromialgia que en sus pares de control (p = 0,03). Hubo una asociación estadísticamente significativa entre la raza y las personas con FM, lo que demuestra que las personas blancas tenían 2,05 veces más probabilidades de desarrollar el síndrome que las personas no blancas (p = 0,03; IC del 95%: 0,93 - 4,53). Hubo una correlación estadísticamente significativa entre la edad y la FM (rS = 0.812, p = 0.01). Este estudio demuestra que las mujeres blancas mayores de 45 años, que tienen el genotipo AA o el alelo A, tienen un mayor riesgo de desarrollar FM, lo que demuestra que este polimorfismo del gen COMT puede ser uno de los factores de riesgo para la fibromialgia.Investigar a influência do polimorfismo de nucleotídeo único (SNP) rs4680 (G / A) da enzima catecol-O-metiltransferase (COMT) na fibromialgia em mulheres. Métodos: Neste estudo observacional do tipo caso-controle 29 mulheres com diagnóstico de FM (casos) e 31 mulheres saudáveis ​​sem fibromialgia (controles). Foram coletados dados sociodemográficos e antropométricos, bem como dados relativos à Escala de Severidade dos Sintomas e Índice Generalizado de Dor e amostras de sangue periférico para extração de DNA; as análises genotípicas foram realizadas por PCR-SSP. Observamos que o genótipo rs4680 AA foi mais frequentemente observado na fibromialgia do que nos controles (p = 0,02). O alelo A também estava mais frequentemente presente nos participantes com fibromialgia do que em seus pares de controle (p = 0,03). Houve associação estatisticamente significativa entre raça e portadores de FM, mostrando que os de raça branca tiveram 2,05 vezes mais chance de desenvolver a síndrome do que os não brancos (p = 0,03; IC 95% 0,93 - 4,53). Observou-se correlação estatisticamente significativa entre idade e FM (rS = 0,812, p = 0,01). Este estudo demonstra que mulheres brancas acima de 45 anos, que possuem o genótipo AA ou alelo A, apresentam maior risco de desenvolver FM, mostrando que esse polimorfismo do gene COMT pode ser um dos fatores de risco para a fibromialgia.Research, Society and Development2021-06-17info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1522510.33448/rsd-v10i7.15225Research, Society and Development; Vol. 10 No. 7; e15010715225Research, Society and Development; Vol. 10 Núm. 7; e15010715225Research, Society and Development; v. 10 n. 7; e150107152252525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/15225/14640Copyright (c) 2021 Stheace Kelly Fernandes Szezerbaty; Carlos Alexandre Martins Zicarelli ; Luana Oliveira de Lima; Priscila Daniele Oliveira Perrucini; Karen Barros Parron Fernandes; Regina Célia Poli-Fredericohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSzezerbaty, Stheace Kelly Fernandes Zicarelli , Carlos Alexandre Martins Lima, Luana Oliveira de Perrucini, Priscila Daniele Oliveira Fernandes, Karen Barros Parron Poli-Frederico, Regina Célia2021-07-18T21:07:03Zoai:ojs.pkp.sfu.ca:article/15225Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:36:06.013811Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
El polimorfismo de un solo nucleótido rs4680 en el gen COMT, la etnia y la edad se asocian con la fibromialgia en las mujeres
Polimorfismo de nucleotídeo único rs4680 no gene COMT, etnia e idade estão associadas com fibromialgia em mulheres
title COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
spellingShingle COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
Szezerbaty, Stheace Kelly Fernandes
Fibromyalgia
Women
Genetic Polymorphism
Pain
Catechol-O-methyltransferase.
Fibromialgia
Mujeres
Polimorfismo genético
Dolor
Catecol-O-metiltransferasa.
Fibromialgia
Mulheres
Polimorfismo genético
Dor
Catecol-O-metiltransferase.
title_short COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
title_full COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
title_fullStr COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
title_full_unstemmed COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
title_sort COMT rs4680 single nucleotide polymorphism, ethnicity, and age are associated with fibromyalgia in women
author Szezerbaty, Stheace Kelly Fernandes
author_facet Szezerbaty, Stheace Kelly Fernandes
Zicarelli , Carlos Alexandre Martins
Lima, Luana Oliveira de
Perrucini, Priscila Daniele Oliveira
Fernandes, Karen Barros Parron
Poli-Frederico, Regina Célia
author_role author
author2 Zicarelli , Carlos Alexandre Martins
Lima, Luana Oliveira de
Perrucini, Priscila Daniele Oliveira
Fernandes, Karen Barros Parron
Poli-Frederico, Regina Célia
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Szezerbaty, Stheace Kelly Fernandes
Zicarelli , Carlos Alexandre Martins
Lima, Luana Oliveira de
Perrucini, Priscila Daniele Oliveira
Fernandes, Karen Barros Parron
Poli-Frederico, Regina Célia
dc.subject.por.fl_str_mv Fibromyalgia
Women
Genetic Polymorphism
Pain
Catechol-O-methyltransferase.
Fibromialgia
Mujeres
Polimorfismo genético
Dolor
Catecol-O-metiltransferasa.
Fibromialgia
Mulheres
Polimorfismo genético
Dor
Catecol-O-metiltransferase.
topic Fibromyalgia
Women
Genetic Polymorphism
Pain
Catechol-O-methyltransferase.
Fibromialgia
Mujeres
Polimorfismo genético
Dolor
Catecol-O-metiltransferasa.
Fibromialgia
Mulheres
Polimorfismo genético
Dor
Catecol-O-metiltransferase.
description To investigate the influence of the catechol-O-methyltransferase enzyme (COMT) single nucleotide polymorphism (SNP) rs4680 (G/A) on fibromyalgia in women. In this observational study of case-control type 29 women with a diagnosis of FM (cases) and 31 healthy non-fibromyalgia women (controls). Sociodemographic and anthropometric data were collected, as well as data relating to Symptom Severity Scale and Generalized Pain Index and peripheral blood samples for DNA extraction; genotypic analyzes were performed by PCR-SSP. We observed that rs4680 AA genotype was more frequently observed in fibromyalgia than controls (p=0.02). The A allele was also more often present in the fibromyalgia participants than in their control peers (p = 0.03). There was a statistically significant association between race and FM sufferers, showing that those of white ethnicity had a 2.05 times greater chance of developing the syndrome than non-white individuals (p=0.03; CI 95% 0.93 – 4.53). A statistically significant correlation between age and FM was observed (rS=0.812, p=0.01). This study demonstrates that white women above the age of 45, who have the AA genotype or A-allele, presents a higher risk of developing FM, showing that this polymorphism of the COMT gene may be one of the risk factors for the fibromyalgia.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-17
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/15225
10.33448/rsd-v10i7.15225
url https://rsdjournal.org/index.php/rsd/article/view/15225
identifier_str_mv 10.33448/rsd-v10i7.15225
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/15225/14640
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 7; e15010715225
Research, Society and Development; Vol. 10 Núm. 7; e15010715225
Research, Society and Development; v. 10 n. 7; e15010715225
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
_version_ 1797052749299318784