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Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis
The aim of the study was an ultrasound assessment of distal interphalangeal (DIP) joint enthesopathy in patients with nail psoriasis. Altogether, 72 patients with nail psoriasis (41 with psoriasis and 31 with psoriatic arthritis) and 30 people in the control group participated in the study. In total...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403314/ https://www.ncbi.nlm.nih.gov/pubmed/30842536 http://dx.doi.org/10.1038/s41598-019-39985-7 |
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author | Krajewska-Włodarczyk, Magdalena Owczarczyk-Saczonek, Agnieszka Placek, Waldemar Wojtkiewicz, Maja Wiktorowicz, Andrzej Wojtkiewicz, Joanna |
author_facet | Krajewska-Włodarczyk, Magdalena Owczarczyk-Saczonek, Agnieszka Placek, Waldemar Wojtkiewicz, Maja Wiktorowicz, Andrzej Wojtkiewicz, Joanna |
author_sort | Krajewska-Włodarczyk, Magdalena |
collection | PubMed |
description | The aim of the study was an ultrasound assessment of distal interphalangeal (DIP) joint enthesopathy in patients with nail psoriasis. Altogether, 72 patients with nail psoriasis (41 with psoriasis and 31 with psoriatic arthritis) and 30 people in the control group participated in the study. In total, 1014 nails were examined. The thickness of DIP digital extensor tendons in the groups of patients with psoriasis (Ps) and psoriatic arthritis (PsA) was correlated with the nail bed thickness (r = 0.316, p = 0.027 vs. r = 0.402, p = 0.031, respectively) and with the thickness of the nail matrix in patients with psoriasis (r = 0.421, p = 0.012). The linear regression model showed the tendon thickness in Ps patients to be affected by the nail bed thickness, duration of psoriasis and the thickness of the nail matrix, whereas in PsA patients it was found to be significantly affected by duration of psoriasis and of arthritis, the nail bed thickness, CRP concentration and the swollen joint count. Our findings may indicate the role of the nail-tendon apparatus changes in the PsA development and they emphasise the justifiability of US examinations in patients with psoriasis direct assessment of morphological changes in nails as potential predictors of PsA development. |
format | Online Article Text |
id | pubmed-6403314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64033142019-03-08 Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis Krajewska-Włodarczyk, Magdalena Owczarczyk-Saczonek, Agnieszka Placek, Waldemar Wojtkiewicz, Maja Wiktorowicz, Andrzej Wojtkiewicz, Joanna Sci Rep Article The aim of the study was an ultrasound assessment of distal interphalangeal (DIP) joint enthesopathy in patients with nail psoriasis. Altogether, 72 patients with nail psoriasis (41 with psoriasis and 31 with psoriatic arthritis) and 30 people in the control group participated in the study. In total, 1014 nails were examined. The thickness of DIP digital extensor tendons in the groups of patients with psoriasis (Ps) and psoriatic arthritis (PsA) was correlated with the nail bed thickness (r = 0.316, p = 0.027 vs. r = 0.402, p = 0.031, respectively) and with the thickness of the nail matrix in patients with psoriasis (r = 0.421, p = 0.012). The linear regression model showed the tendon thickness in Ps patients to be affected by the nail bed thickness, duration of psoriasis and the thickness of the nail matrix, whereas in PsA patients it was found to be significantly affected by duration of psoriasis and of arthritis, the nail bed thickness, CRP concentration and the swollen joint count. Our findings may indicate the role of the nail-tendon apparatus changes in the PsA development and they emphasise the justifiability of US examinations in patients with psoriasis direct assessment of morphological changes in nails as potential predictors of PsA development. Nature Publishing Group UK 2019-03-06 /pmc/articles/PMC6403314/ /pubmed/30842536 http://dx.doi.org/10.1038/s41598-019-39985-7 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Krajewska-Włodarczyk, Magdalena Owczarczyk-Saczonek, Agnieszka Placek, Waldemar Wojtkiewicz, Maja Wiktorowicz, Andrzej Wojtkiewicz, Joanna Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title | Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title_full | Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title_fullStr | Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title_full_unstemmed | Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title_short | Distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
title_sort | distal interphalangeal joint extensor tendon enthesopathy in patients with nail psoriasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403314/ https://www.ncbi.nlm.nih.gov/pubmed/30842536 http://dx.doi.org/10.1038/s41598-019-39985-7 |
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