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Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study

BACKGROUND: High levels of the tumor necrosis factor alpha (TNF-α) induce apoptosis and pro-inflammatory effects for primary degeneration of tendon and development of tendinopathy. The aim of this study was to investigate the association between the TNF-α polymorphisms and tendinopathy in athletes....

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Autores principales: Lopes, Lucas Rafael, de Miranda, Vitor Almeida Ribeiro, Guimarães, João Antonio Matheus, de Araujo Souza, Gabriel Garcez, Wainchtock, Victor Soares, Grangeiro Neto, João Alves, de Araújo Goes, Rodrigo, Perini, Jamila Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117576/
https://www.ncbi.nlm.nih.gov/pubmed/33985554
http://dx.doi.org/10.1186/s13102-021-00276-2
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author Lopes, Lucas Rafael
de Miranda, Vitor Almeida Ribeiro
Guimarães, João Antonio Matheus
de Araujo Souza, Gabriel Garcez
Wainchtock, Victor Soares
Grangeiro Neto, João Alves
de Araújo Goes, Rodrigo
Perini, Jamila Alessandra
author_facet Lopes, Lucas Rafael
de Miranda, Vitor Almeida Ribeiro
Guimarães, João Antonio Matheus
de Araujo Souza, Gabriel Garcez
Wainchtock, Victor Soares
Grangeiro Neto, João Alves
de Araújo Goes, Rodrigo
Perini, Jamila Alessandra
author_sort Lopes, Lucas Rafael
collection PubMed
description BACKGROUND: High levels of the tumor necrosis factor alpha (TNF-α) induce apoptosis and pro-inflammatory effects for primary degeneration of tendon and development of tendinopathy. The aim of this study was to investigate the association between the TNF-α polymorphisms and tendinopathy in athletes. METHODS: Two hundred and seventy athletes (135 tendinopathy cases and 135 controls) were included and genotyped (TNF-α -1031T > C; -857 C > T; -308G > A) using TaqMan validated assays. The association of the polymorphisms with tendinopathy was evaluated by a multivariate logistic regression model, using odds ratios (OR) and 95 % confidence intervals (CI). RESULTS: The variant allele − 308 A was significantly associated with patellar (OR: 1.9; 95 % CI: 1.01–3.6) or Achilles tendinopathies (OR: 2.7; 95 % CI: 1.1–6.7). No significant differences were found in allele or genotype distributions of the − 1031T > C and − 857 C > T polymorphisms between cases and controls. TNF-α TCA haplotype was associated with increased tendinopathies risk, either considering all cases (OR: 2.6, 95 % CI: 1.3–5.3), patellar (OR: 3.3, 95 % CI: 1.5–7.3), rotator cuff (OR: 3.1, 95 % CI: 1.4–7.2) or Achilles tendinopathies (OR: 3.8, 95 % CI: 1.1–12.7). CONCLUSIONS: These results suggest that the TNF-α polymorphisms could influence the susceptibility to developing tendinopathy among athletes. Knowledge of the TNF-α polymorphisms associated to tendinopathy in athletes can further understanding of the inflammatory role in the early stages of the disease and contribute for sports injury surveillance programmes, in which athletes with TNF-α TCA haplotype could be early subjected to cryotherapy after training and competition to avoid tendinopathy development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13102-021-00276-2.
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spelling pubmed-81175762021-05-13 Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study Lopes, Lucas Rafael de Miranda, Vitor Almeida Ribeiro Guimarães, João Antonio Matheus de Araujo Souza, Gabriel Garcez Wainchtock, Victor Soares Grangeiro Neto, João Alves de Araújo Goes, Rodrigo Perini, Jamila Alessandra BMC Sports Sci Med Rehabil Research Article BACKGROUND: High levels of the tumor necrosis factor alpha (TNF-α) induce apoptosis and pro-inflammatory effects for primary degeneration of tendon and development of tendinopathy. The aim of this study was to investigate the association between the TNF-α polymorphisms and tendinopathy in athletes. METHODS: Two hundred and seventy athletes (135 tendinopathy cases and 135 controls) were included and genotyped (TNF-α -1031T > C; -857 C > T; -308G > A) using TaqMan validated assays. The association of the polymorphisms with tendinopathy was evaluated by a multivariate logistic regression model, using odds ratios (OR) and 95 % confidence intervals (CI). RESULTS: The variant allele − 308 A was significantly associated with patellar (OR: 1.9; 95 % CI: 1.01–3.6) or Achilles tendinopathies (OR: 2.7; 95 % CI: 1.1–6.7). No significant differences were found in allele or genotype distributions of the − 1031T > C and − 857 C > T polymorphisms between cases and controls. TNF-α TCA haplotype was associated with increased tendinopathies risk, either considering all cases (OR: 2.6, 95 % CI: 1.3–5.3), patellar (OR: 3.3, 95 % CI: 1.5–7.3), rotator cuff (OR: 3.1, 95 % CI: 1.4–7.2) or Achilles tendinopathies (OR: 3.8, 95 % CI: 1.1–12.7). CONCLUSIONS: These results suggest that the TNF-α polymorphisms could influence the susceptibility to developing tendinopathy among athletes. Knowledge of the TNF-α polymorphisms associated to tendinopathy in athletes can further understanding of the inflammatory role in the early stages of the disease and contribute for sports injury surveillance programmes, in which athletes with TNF-α TCA haplotype could be early subjected to cryotherapy after training and competition to avoid tendinopathy development. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13102-021-00276-2. BioMed Central 2021-05-13 /pmc/articles/PMC8117576/ /pubmed/33985554 http://dx.doi.org/10.1186/s13102-021-00276-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lopes, Lucas Rafael
de Miranda, Vitor Almeida Ribeiro
Guimarães, João Antonio Matheus
de Araujo Souza, Gabriel Garcez
Wainchtock, Victor Soares
Grangeiro Neto, João Alves
de Araújo Goes, Rodrigo
Perini, Jamila Alessandra
Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title_full Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title_fullStr Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title_full_unstemmed Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title_short Association of TNF-α -308G > A polymorphism with susceptibility to tendinopathy in athletes: a case–control study
title_sort association of tnf-α -308g > a polymorphism with susceptibility to tendinopathy in athletes: a case–control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117576/
https://www.ncbi.nlm.nih.gov/pubmed/33985554
http://dx.doi.org/10.1186/s13102-021-00276-2
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