Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/110152 |
Resumo: | Background: Fibromyalgia (FM) is conceptualized as a central sensitization (CS) condition, that presents high serum brain-derived neurotrophic factor (BDNF) and neuroglia activation. Although the S100B protein regulates neuroglia functions, it has been traditionally used as a proxy of central nervous system damage. However, neither BDNF nor S100B association with the clinical picture of FM has been elucidated. To explore their association with the pressure-pain threshold (PPT) in FM, we performed a cross-sectional study, including 56 females with confirmed FM aged 18–65 years. Linear regression models were used to adjust for potential confounding factors between serum BDNF, S100B and PPT. Results: Serum BDNF and S100B were correlated (Spearman’s Rho = 0.29). Serum BDNF (log) and S100B (log) were correlated with the PPT (log) (Partial η2 = 0.129, P = 0.012 for the BDNF (log), and Partial η2 = 0.105, P = 0.025 for the S100B (log)). Serum BDNF (log) was inversely associated with PPT (log) (β = −1.01, SE = 0.41), age (β = −0.02, SE = 0.15) and obsessive compulsive disorder (β = −0.36, SE = 0.15), while serum S100B (log) was inversely associated with PPT (log) (β = −1.38, SE = 0.50), only. Conclusions: Both neuroglia key mediators in the CS process were inversely correlated with the PPT. Serum assessment of BDNF and S100B deserve further study to determine its potential as a proxy for the CS spectrum in FM. |
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Zanette, Simone de AzevedoSarria, Jairo Alberto DussánSouza, Andressa deDeitos, AlíciaTorres, Iraci Lucena da SilvaCaumo, Wolnei2015-02-14T02:19:07Z20141744-8069http://hdl.handle.net/10183/110152000929928Background: Fibromyalgia (FM) is conceptualized as a central sensitization (CS) condition, that presents high serum brain-derived neurotrophic factor (BDNF) and neuroglia activation. Although the S100B protein regulates neuroglia functions, it has been traditionally used as a proxy of central nervous system damage. However, neither BDNF nor S100B association with the clinical picture of FM has been elucidated. To explore their association with the pressure-pain threshold (PPT) in FM, we performed a cross-sectional study, including 56 females with confirmed FM aged 18–65 years. Linear regression models were used to adjust for potential confounding factors between serum BDNF, S100B and PPT. Results: Serum BDNF and S100B were correlated (Spearman’s Rho = 0.29). Serum BDNF (log) and S100B (log) were correlated with the PPT (log) (Partial η2 = 0.129, P = 0.012 for the BDNF (log), and Partial η2 = 0.105, P = 0.025 for the S100B (log)). Serum BDNF (log) was inversely associated with PPT (log) (β = −1.01, SE = 0.41), age (β = −0.02, SE = 0.15) and obsessive compulsive disorder (β = −0.36, SE = 0.15), while serum S100B (log) was inversely associated with PPT (log) (β = −1.38, SE = 0.50), only. Conclusions: Both neuroglia key mediators in the CS process were inversely correlated with the PPT. Serum assessment of BDNF and S100B deserve further study to determine its potential as a proxy for the CS spectrum in FM.application/pdfengMolecular pain. [London]. Vol. 10 (8 Jul. 2014), p. 46, 9 p.FibromialgiaProteínas S100Fator neurotrófico derivado do encéfaloLimiar da dorFibromyalgiaS100BBDNFPain-pressure thresholdCentral sensitizationHigher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgiaEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000929928.pdf000929928.pdfTexto completo (inglês)application/pdf371343http://www.lume.ufrgs.br/bitstream/10183/110152/1/000929928.pdf4482d0f7ce621537bf79667d4b9aa944MD51TEXT000929928.pdf.txt000929928.pdf.txtExtracted Texttext/plain41257http://www.lume.ufrgs.br/bitstream/10183/110152/2/000929928.pdf.txt5c096af1efb595150e6647ed973ceb91MD52THUMBNAIL000929928.pdf.jpg000929928.pdf.jpgGenerated Thumbnailimage/jpeg1937http://www.lume.ufrgs.br/bitstream/10183/110152/3/000929928.pdf.jpg64d918064bee2b1439d9de363976ed43MD5310183/1101522019-01-11 04:08:50.577679oai:www.lume.ufrgs.br:10183/110152Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2019-01-11T06:08:50Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
title |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
spellingShingle |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia Zanette, Simone de Azevedo Fibromialgia Proteínas S100 Fator neurotrófico derivado do encéfalo Limiar da dor Fibromyalgia S100B BDNF Pain-pressure threshold Central sensitization |
title_short |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
title_full |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
title_fullStr |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
title_full_unstemmed |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
title_sort |
Higher serum S100b and BDNF levels are correlated with a lower pressure-pain threshold in fibromyalgia |
author |
Zanette, Simone de Azevedo |
author_facet |
Zanette, Simone de Azevedo Sarria, Jairo Alberto Dussán Souza, Andressa de Deitos, Alícia Torres, Iraci Lucena da Silva Caumo, Wolnei |
author_role |
author |
author2 |
Sarria, Jairo Alberto Dussán Souza, Andressa de Deitos, Alícia Torres, Iraci Lucena da Silva Caumo, Wolnei |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Zanette, Simone de Azevedo Sarria, Jairo Alberto Dussán Souza, Andressa de Deitos, Alícia Torres, Iraci Lucena da Silva Caumo, Wolnei |
dc.subject.por.fl_str_mv |
Fibromialgia Proteínas S100 Fator neurotrófico derivado do encéfalo Limiar da dor |
topic |
Fibromialgia Proteínas S100 Fator neurotrófico derivado do encéfalo Limiar da dor Fibromyalgia S100B BDNF Pain-pressure threshold Central sensitization |
dc.subject.eng.fl_str_mv |
Fibromyalgia S100B BDNF Pain-pressure threshold Central sensitization |
description |
Background: Fibromyalgia (FM) is conceptualized as a central sensitization (CS) condition, that presents high serum brain-derived neurotrophic factor (BDNF) and neuroglia activation. Although the S100B protein regulates neuroglia functions, it has been traditionally used as a proxy of central nervous system damage. However, neither BDNF nor S100B association with the clinical picture of FM has been elucidated. To explore their association with the pressure-pain threshold (PPT) in FM, we performed a cross-sectional study, including 56 females with confirmed FM aged 18–65 years. Linear regression models were used to adjust for potential confounding factors between serum BDNF, S100B and PPT. Results: Serum BDNF and S100B were correlated (Spearman’s Rho = 0.29). Serum BDNF (log) and S100B (log) were correlated with the PPT (log) (Partial η2 = 0.129, P = 0.012 for the BDNF (log), and Partial η2 = 0.105, P = 0.025 for the S100B (log)). Serum BDNF (log) was inversely associated with PPT (log) (β = −1.01, SE = 0.41), age (β = −0.02, SE = 0.15) and obsessive compulsive disorder (β = −0.36, SE = 0.15), while serum S100B (log) was inversely associated with PPT (log) (β = −1.38, SE = 0.50), only. Conclusions: Both neuroglia key mediators in the CS process were inversely correlated with the PPT. Serum assessment of BDNF and S100B deserve further study to determine its potential as a proxy for the CS spectrum in FM. |
publishDate |
2014 |
dc.date.issued.fl_str_mv |
2014 |
dc.date.accessioned.fl_str_mv |
2015-02-14T02:19:07Z |
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http://hdl.handle.net/10183/110152 |
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1744-8069 |
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000929928 |
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eng |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Molecular pain. [London]. Vol. 10 (8 Jul. 2014), p. 46, 9 p. |
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openAccess |
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