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Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability

BACKGROUND: Disability of the shoulder joint is often caused by a tear in the rotator cuff (RC) muscles. Four RC muscles coordinate shoulder movement and stability, among them the supraspinatus and infraspinatus muscle which are predominantly torn. The contribution of each RC muscle to tear patholog...

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Autores principales: Henseler, Jan F., Raz, Yotam, Nagels, Jochem, van Zwet, Erik W., Raz, Vered, Nelissen, Rob G. H. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339721/
https://www.ncbi.nlm.nih.gov/pubmed/25710703
http://dx.doi.org/10.1371/journal.pone.0118158
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author Henseler, Jan F.
Raz, Yotam
Nagels, Jochem
van Zwet, Erik W.
Raz, Vered
Nelissen, Rob G. H. H.
author_facet Henseler, Jan F.
Raz, Yotam
Nagels, Jochem
van Zwet, Erik W.
Raz, Vered
Nelissen, Rob G. H. H.
author_sort Henseler, Jan F.
collection PubMed
description BACKGROUND: Disability of the shoulder joint is often caused by a tear in the rotator cuff (RC) muscles. Four RC muscles coordinate shoulder movement and stability, among them the supraspinatus and infraspinatus muscle which are predominantly torn. The contribution of each RC muscle to tear pathology is not fully understood. We hypothesized that muscle atrophy and fatty infiltration, features of RC muscle degeneration, are predictive of superior humeral head translation and shoulder functional disability. METHODS: Shoulder features, including RC muscle surface area and fatty infiltration, superior humeral translation and RC tear size were obtained from a consecutive series of Magnetic Resonance Imaging with arthrography (MRA). We investigated patients with superior (supraspinatus, n = 39) and posterosuperior (supraspinatus and infraspinatus, n = 30) RC tears, and patients with an intact RC (n = 52) as controls. The individual or combinatorial contribution of RC measures to superior humeral translation, as a sign of RC dysfunction, was investigated with univariate or multivariate models, respectively. RESULTS: Using the univariate model the infraspinatus surface area and fatty infiltration in both the supraspinatus and infraspinatus had a significant contribution to RC dysfunction. With the multivariate model, however, the infraspinatus surface area only affected superior humeral translation (p<0.001) and discriminated between superior and posterosuperior tears. In contrast neither tear size nor fatty infiltration of the supraspinatus or infraspinatus contributed to superior humeral translation. CONCLUSION: Our study reveals that infraspinatus atrophy has the strongest contribution to RC tear pathologies. This suggests a pivotal role for the infraspinatus in preventing shoulder disability.
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spelling pubmed-43397212015-03-04 Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability Henseler, Jan F. Raz, Yotam Nagels, Jochem van Zwet, Erik W. Raz, Vered Nelissen, Rob G. H. H. PLoS One Research Article BACKGROUND: Disability of the shoulder joint is often caused by a tear in the rotator cuff (RC) muscles. Four RC muscles coordinate shoulder movement and stability, among them the supraspinatus and infraspinatus muscle which are predominantly torn. The contribution of each RC muscle to tear pathology is not fully understood. We hypothesized that muscle atrophy and fatty infiltration, features of RC muscle degeneration, are predictive of superior humeral head translation and shoulder functional disability. METHODS: Shoulder features, including RC muscle surface area and fatty infiltration, superior humeral translation and RC tear size were obtained from a consecutive series of Magnetic Resonance Imaging with arthrography (MRA). We investigated patients with superior (supraspinatus, n = 39) and posterosuperior (supraspinatus and infraspinatus, n = 30) RC tears, and patients with an intact RC (n = 52) as controls. The individual or combinatorial contribution of RC measures to superior humeral translation, as a sign of RC dysfunction, was investigated with univariate or multivariate models, respectively. RESULTS: Using the univariate model the infraspinatus surface area and fatty infiltration in both the supraspinatus and infraspinatus had a significant contribution to RC dysfunction. With the multivariate model, however, the infraspinatus surface area only affected superior humeral translation (p<0.001) and discriminated between superior and posterosuperior tears. In contrast neither tear size nor fatty infiltration of the supraspinatus or infraspinatus contributed to superior humeral translation. CONCLUSION: Our study reveals that infraspinatus atrophy has the strongest contribution to RC tear pathologies. This suggests a pivotal role for the infraspinatus in preventing shoulder disability. Public Library of Science 2015-02-24 /pmc/articles/PMC4339721/ /pubmed/25710703 http://dx.doi.org/10.1371/journal.pone.0118158 Text en © 2015 Henseler et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Henseler, Jan F.
Raz, Yotam
Nagels, Jochem
van Zwet, Erik W.
Raz, Vered
Nelissen, Rob G. H. H.
Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title_full Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title_fullStr Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title_full_unstemmed Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title_short Multivariate Analyses of Rotator Cuff Pathologies in Shoulder Disability
title_sort multivariate analyses of rotator cuff pathologies in shoulder disability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339721/
https://www.ncbi.nlm.nih.gov/pubmed/25710703
http://dx.doi.org/10.1371/journal.pone.0118158
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