Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/225180 |
Resumo: | Background: Fibromyalgia (FM) is a musculoskeletal chronic pain syndrome that impacts negatively patient’s daily lives. Its pathogenesis is characterized by a complex relationship between biological and psychosocial factors not fully understood yet. Pain catastrophizing is associated with FM and is an important predictor of outcomes. This study aimed to answer two questions: (i) whether the allele and genotype frequencies of BDNF Val66Met (rs6265) polymorphism differs between FM patients and healthy controls (HC); and (ii) if the BDNF Val66Met polymorphism is a factor that predicts pain catastrophizing in FM. Methods: In a cross-sectional design, 108 FM patients and 108 HC were included. FM patients responded to the Brazilian Portuguese version of the Pain Catastrophizing Scale (BP-PCS) to assess pain catastrophizing, as well as other validated tools for anxiety (The State-Trait Anxiety Inventory - STAI), depression (Beck Depression Inventory II – BDI-II) and functional aspects (Fibromyalgia Impact Questionnaire - FIQ; Central Sensitization Inventory validated and adapted for Brazilian population - CSI-BP; Pittsburgh Sleep Quality Index - PSQI; and Resilience Scale). All subjects were genotyped for the BDNF Val66Met polymorphism. Results: Val allele was significantly more frequent in FM patients compared to the control group (p < 0.05). Also, FM patients with Val/Val genotype showed more pain catastrophizing thoughts, and this genotype was significantly associated with magnification and rumination dimensions of BP-PCS (p < 0.05). Furthermore, there were significant differences in levels of anxiety and symptoms of depression, years of education, and the functional situation between the FM and control groups. Conclusions: The findings show an association of BDNF Val66Met polymorphism with pain catastrophizing in FM, which opens new avenues to comprehend the interplay between molecular genetic characteristics and neuroplasticity mechanisms underpinning FM. |
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Alves, Camila Fernanda da SilveiraCaumo, WolneiSilvestri, Joana MorezZortéa, MaxcielSantos, Vinícius Souza dosCardoso, Dayane FavarinRegner, Andrea PereiraSouza, Alessandra Hubner deSimon, Daniel2021-08-05T04:30:29Z20202523-3106http://hdl.handle.net/10183/225180001129240Background: Fibromyalgia (FM) is a musculoskeletal chronic pain syndrome that impacts negatively patient’s daily lives. Its pathogenesis is characterized by a complex relationship between biological and psychosocial factors not fully understood yet. Pain catastrophizing is associated with FM and is an important predictor of outcomes. This study aimed to answer two questions: (i) whether the allele and genotype frequencies of BDNF Val66Met (rs6265) polymorphism differs between FM patients and healthy controls (HC); and (ii) if the BDNF Val66Met polymorphism is a factor that predicts pain catastrophizing in FM. Methods: In a cross-sectional design, 108 FM patients and 108 HC were included. FM patients responded to the Brazilian Portuguese version of the Pain Catastrophizing Scale (BP-PCS) to assess pain catastrophizing, as well as other validated tools for anxiety (The State-Trait Anxiety Inventory - STAI), depression (Beck Depression Inventory II – BDI-II) and functional aspects (Fibromyalgia Impact Questionnaire - FIQ; Central Sensitization Inventory validated and adapted for Brazilian population - CSI-BP; Pittsburgh Sleep Quality Index - PSQI; and Resilience Scale). All subjects were genotyped for the BDNF Val66Met polymorphism. Results: Val allele was significantly more frequent in FM patients compared to the control group (p < 0.05). Also, FM patients with Val/Val genotype showed more pain catastrophizing thoughts, and this genotype was significantly associated with magnification and rumination dimensions of BP-PCS (p < 0.05). Furthermore, there were significant differences in levels of anxiety and symptoms of depression, years of education, and the functional situation between the FM and control groups. Conclusions: The findings show an association of BDNF Val66Met polymorphism with pain catastrophizing in FM, which opens new avenues to comprehend the interplay between molecular genetic characteristics and neuroplasticity mechanisms underpinning FM.application/pdfengAdvances in rheumatology. São Paulo. Vol. 60 (2020), 39, 9 p.FibromialgiaPolimorfismo genéticoFator neurotrófico derivado do encéfaloCatastrofizaçãoDorFibromyalgiaPain catastrophizingBDNFSingle nucleotide polymorphismVal66MetPain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgiainfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001129240.pdf.txt001129240.pdf.txtExtracted Texttext/plain43625http://www.lume.ufrgs.br/bitstream/10183/225180/2/001129240.pdf.txte82e2ad6169181a2cb00559ac6549f81MD52ORIGINAL001129240.pdfTexto completo (inglês)application/pdf797488http://www.lume.ufrgs.br/bitstream/10183/225180/1/001129240.pdf5b4854b6db19c7539606ff0606df9341MD5110183/2251802023-05-24 03:26:00.543061oai:www.lume.ufrgs.br:10183/225180Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-05-24T06:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
title |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
spellingShingle |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia Alves, Camila Fernanda da Silveira Fibromialgia Polimorfismo genético Fator neurotrófico derivado do encéfalo Catastrofização Dor Fibromyalgia Pain catastrophizing BDNF Single nucleotide polymorphism Val66Met |
title_short |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
title_full |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
title_fullStr |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
title_full_unstemmed |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
title_sort |
Pain catastrophizing is associated with the Val66Met polymorphism of the brainderived neurotrophic factor in fibromyalgia |
author |
Alves, Camila Fernanda da Silveira |
author_facet |
Alves, Camila Fernanda da Silveira Caumo, Wolnei Silvestri, Joana Morez Zortéa, Maxciel Santos, Vinícius Souza dos Cardoso, Dayane Favarin Regner, Andrea Pereira Souza, Alessandra Hubner de Simon, Daniel |
author_role |
author |
author2 |
Caumo, Wolnei Silvestri, Joana Morez Zortéa, Maxciel Santos, Vinícius Souza dos Cardoso, Dayane Favarin Regner, Andrea Pereira Souza, Alessandra Hubner de Simon, Daniel |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Alves, Camila Fernanda da Silveira Caumo, Wolnei Silvestri, Joana Morez Zortéa, Maxciel Santos, Vinícius Souza dos Cardoso, Dayane Favarin Regner, Andrea Pereira Souza, Alessandra Hubner de Simon, Daniel |
dc.subject.por.fl_str_mv |
Fibromialgia Polimorfismo genético Fator neurotrófico derivado do encéfalo Catastrofização Dor |
topic |
Fibromialgia Polimorfismo genético Fator neurotrófico derivado do encéfalo Catastrofização Dor Fibromyalgia Pain catastrophizing BDNF Single nucleotide polymorphism Val66Met |
dc.subject.eng.fl_str_mv |
Fibromyalgia Pain catastrophizing BDNF Single nucleotide polymorphism Val66Met |
description |
Background: Fibromyalgia (FM) is a musculoskeletal chronic pain syndrome that impacts negatively patient’s daily lives. Its pathogenesis is characterized by a complex relationship between biological and psychosocial factors not fully understood yet. Pain catastrophizing is associated with FM and is an important predictor of outcomes. This study aimed to answer two questions: (i) whether the allele and genotype frequencies of BDNF Val66Met (rs6265) polymorphism differs between FM patients and healthy controls (HC); and (ii) if the BDNF Val66Met polymorphism is a factor that predicts pain catastrophizing in FM. Methods: In a cross-sectional design, 108 FM patients and 108 HC were included. FM patients responded to the Brazilian Portuguese version of the Pain Catastrophizing Scale (BP-PCS) to assess pain catastrophizing, as well as other validated tools for anxiety (The State-Trait Anxiety Inventory - STAI), depression (Beck Depression Inventory II – BDI-II) and functional aspects (Fibromyalgia Impact Questionnaire - FIQ; Central Sensitization Inventory validated and adapted for Brazilian population - CSI-BP; Pittsburgh Sleep Quality Index - PSQI; and Resilience Scale). All subjects were genotyped for the BDNF Val66Met polymorphism. Results: Val allele was significantly more frequent in FM patients compared to the control group (p < 0.05). Also, FM patients with Val/Val genotype showed more pain catastrophizing thoughts, and this genotype was significantly associated with magnification and rumination dimensions of BP-PCS (p < 0.05). Furthermore, there were significant differences in levels of anxiety and symptoms of depression, years of education, and the functional situation between the FM and control groups. Conclusions: The findings show an association of BDNF Val66Met polymorphism with pain catastrophizing in FM, which opens new avenues to comprehend the interplay between molecular genetic characteristics and neuroplasticity mechanisms underpinning FM. |
publishDate |
2020 |
dc.date.issued.fl_str_mv |
2020 |
dc.date.accessioned.fl_str_mv |
2021-08-05T04:30:29Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
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publishedVersion |
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http://hdl.handle.net/10183/225180 |
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2523-3106 |
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001129240 |
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2523-3106 001129240 |
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http://hdl.handle.net/10183/225180 |
dc.language.iso.fl_str_mv |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Advances in rheumatology. São Paulo. Vol. 60 (2020), 39, 9 p. |
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