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Relationship between Alexithymia and latent trigger points in the upper Trapezius

BACKGROUND: Latent trigger points (LTrPs) can be activated by future events, leading to pain. Few studies have reported LTrP risk factors. It has been suggested that alexithymia is associated with myofascial pain and diminished awareness of physical sensation. This study was designed to evaluate the...

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Autores principales: Hasuo, Hideaki, Kanbara, Kenji, Abe, Tetsuya, Fukunaga, Mikihiko, Yunoki, Naoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725834/
https://www.ncbi.nlm.nih.gov/pubmed/29238400
http://dx.doi.org/10.1186/s13030-017-0116-6
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author Hasuo, Hideaki
Kanbara, Kenji
Abe, Tetsuya
Fukunaga, Mikihiko
Yunoki, Naoko
author_facet Hasuo, Hideaki
Kanbara, Kenji
Abe, Tetsuya
Fukunaga, Mikihiko
Yunoki, Naoko
author_sort Hasuo, Hideaki
collection PubMed
description BACKGROUND: Latent trigger points (LTrPs) can be activated by future events, leading to pain. Few studies have reported LTrP risk factors. It has been suggested that alexithymia is associated with myofascial pain and diminished awareness of physical sensation. This study was designed to evaluate the relation between alexithymia and LTrPs found the upper trapezius of healthy individuals. METHODS: The correlation between LTrPs and alexithymia, and between LTrPs and depression was analyzed in 160 healthy participants (80 male, mean age: 40.5 years [20 to 66 years]). Each participant was evaluated for potential LTrPs by careful manual examination and completed the Toronto Alexithymia Scale-20 (TAS-20) and the Beck Depression Inventory (BDI) to assess potential alexithymia and depressive symptoms, respectively. RESULTS: LTrPs were observed in the upper trapezius of 76 participants (47.5%). TAS-20 scores were significantly higher in subjects with LTrPs than without LTrPs (p < 0.001); in contrast, there was no significant BDI score difference between these groups (p = 0.451). The LTrP risk for alexithymia was 2.74 (95% confidence interval [95% CI]: 2.10–3.58). There was no correlation between the TAS-20 and BDI scores (correlation coefficient: −0.04). Significant risk factors associated with LTrPs included the TAS-20 score (odds ratio [OR]: 1.11, 95% CI: 1.07–1.15) and age (OR: 1.05, 95% CI: 1.01–1.09). CONCLUSIONS: Alexithymia was associated with LTrPs in the upper trapezius of healthy individuals, suggesting that it may serve as a useful predictive factor. TRIAL REGISTRATION: UMIN000027468. Registered 23 May 2017(retrospectively registered).
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spelling pubmed-57258342017-12-13 Relationship between Alexithymia and latent trigger points in the upper Trapezius Hasuo, Hideaki Kanbara, Kenji Abe, Tetsuya Fukunaga, Mikihiko Yunoki, Naoko Biopsychosoc Med Research BACKGROUND: Latent trigger points (LTrPs) can be activated by future events, leading to pain. Few studies have reported LTrP risk factors. It has been suggested that alexithymia is associated with myofascial pain and diminished awareness of physical sensation. This study was designed to evaluate the relation between alexithymia and LTrPs found the upper trapezius of healthy individuals. METHODS: The correlation between LTrPs and alexithymia, and between LTrPs and depression was analyzed in 160 healthy participants (80 male, mean age: 40.5 years [20 to 66 years]). Each participant was evaluated for potential LTrPs by careful manual examination and completed the Toronto Alexithymia Scale-20 (TAS-20) and the Beck Depression Inventory (BDI) to assess potential alexithymia and depressive symptoms, respectively. RESULTS: LTrPs were observed in the upper trapezius of 76 participants (47.5%). TAS-20 scores were significantly higher in subjects with LTrPs than without LTrPs (p < 0.001); in contrast, there was no significant BDI score difference between these groups (p = 0.451). The LTrP risk for alexithymia was 2.74 (95% confidence interval [95% CI]: 2.10–3.58). There was no correlation between the TAS-20 and BDI scores (correlation coefficient: −0.04). Significant risk factors associated with LTrPs included the TAS-20 score (odds ratio [OR]: 1.11, 95% CI: 1.07–1.15) and age (OR: 1.05, 95% CI: 1.01–1.09). CONCLUSIONS: Alexithymia was associated with LTrPs in the upper trapezius of healthy individuals, suggesting that it may serve as a useful predictive factor. TRIAL REGISTRATION: UMIN000027468. Registered 23 May 2017(retrospectively registered). BioMed Central 2017-12-11 /pmc/articles/PMC5725834/ /pubmed/29238400 http://dx.doi.org/10.1186/s13030-017-0116-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Hasuo, Hideaki
Kanbara, Kenji
Abe, Tetsuya
Fukunaga, Mikihiko
Yunoki, Naoko
Relationship between Alexithymia and latent trigger points in the upper Trapezius
title Relationship between Alexithymia and latent trigger points in the upper Trapezius
title_full Relationship between Alexithymia and latent trigger points in the upper Trapezius
title_fullStr Relationship between Alexithymia and latent trigger points in the upper Trapezius
title_full_unstemmed Relationship between Alexithymia and latent trigger points in the upper Trapezius
title_short Relationship between Alexithymia and latent trigger points in the upper Trapezius
title_sort relationship between alexithymia and latent trigger points in the upper trapezius
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725834/
https://www.ncbi.nlm.nih.gov/pubmed/29238400
http://dx.doi.org/10.1186/s13030-017-0116-6
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