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Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations

To explore the influence of dermatomyositis (DM)-specific cutaneous manifestations (scm) on systemic coagulation and fibrinolysis, we retrospectively studied plasma D-dimer levels with/without venous thromboembolism (VTE), malignancy, infection or other connective tissue diseases (CTDs) and scm. One...

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Autores principales: Habe, Koji, Wada, Hideo, Higashiyama, Ayaka, Akeda, Tomoko, Tsuda, Kenshiro, Mori, Ryoko, Kakeda, Masato, Yamanaka, Keiichi, Mizutani, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363793/
https://www.ncbi.nlm.nih.gov/pubmed/30723246
http://dx.doi.org/10.1038/s41598-018-38108-y
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author Habe, Koji
Wada, Hideo
Higashiyama, Ayaka
Akeda, Tomoko
Tsuda, Kenshiro
Mori, Ryoko
Kakeda, Masato
Yamanaka, Keiichi
Mizutani, Hitoshi
author_facet Habe, Koji
Wada, Hideo
Higashiyama, Ayaka
Akeda, Tomoko
Tsuda, Kenshiro
Mori, Ryoko
Kakeda, Masato
Yamanaka, Keiichi
Mizutani, Hitoshi
author_sort Habe, Koji
collection PubMed
description To explore the influence of dermatomyositis (DM)-specific cutaneous manifestations (scm) on systemic coagulation and fibrinolysis, we retrospectively studied plasma D-dimer levels with/without venous thromboembolism (VTE), malignancy, infection or other connective tissue diseases (CTDs) and scm. One hundred fifty patients with DM were retrospectively investigated using medical records regarding scm, VTE, malignancy, infection, other CTDs, laboratory data and systemic corticosteroid therapy. All DM patients were categorized as follows: group 1, without scm, VTE, infection, malignancy or other accompanying CTDs; group 2, with scm only; and group 3, with VTE, infection, malignancy and other accompanying CTDs but without scm. The D-dimer plasma levels were significantly increased in group 3 compared with healthy subjects and those in groups 1 and 2 (p < 0.001). The D-dimer plasma level in group 2 was significantly increased compared with healthy subjects and those in group 1 (p < 0.001). Increased D-dimer plasma levels were detected in DM patients with scm without detectable VTE, malignancy, infection or accompanying CTDs. In addition to the known risk factors for increased plasma D-dimer levels in DM patients, including VTE, malignancy, infection and other accompanying autoimmune diseases, the presence of cutaneous manifestations should be considered as a new clinical risk factor.
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spelling pubmed-63637932019-02-07 Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations Habe, Koji Wada, Hideo Higashiyama, Ayaka Akeda, Tomoko Tsuda, Kenshiro Mori, Ryoko Kakeda, Masato Yamanaka, Keiichi Mizutani, Hitoshi Sci Rep Article To explore the influence of dermatomyositis (DM)-specific cutaneous manifestations (scm) on systemic coagulation and fibrinolysis, we retrospectively studied plasma D-dimer levels with/without venous thromboembolism (VTE), malignancy, infection or other connective tissue diseases (CTDs) and scm. One hundred fifty patients with DM were retrospectively investigated using medical records regarding scm, VTE, malignancy, infection, other CTDs, laboratory data and systemic corticosteroid therapy. All DM patients were categorized as follows: group 1, without scm, VTE, infection, malignancy or other accompanying CTDs; group 2, with scm only; and group 3, with VTE, infection, malignancy and other accompanying CTDs but without scm. The D-dimer plasma levels were significantly increased in group 3 compared with healthy subjects and those in groups 1 and 2 (p < 0.001). The D-dimer plasma level in group 2 was significantly increased compared with healthy subjects and those in group 1 (p < 0.001). Increased D-dimer plasma levels were detected in DM patients with scm without detectable VTE, malignancy, infection or accompanying CTDs. In addition to the known risk factors for increased plasma D-dimer levels in DM patients, including VTE, malignancy, infection and other accompanying autoimmune diseases, the presence of cutaneous manifestations should be considered as a new clinical risk factor. Nature Publishing Group UK 2019-02-05 /pmc/articles/PMC6363793/ /pubmed/30723246 http://dx.doi.org/10.1038/s41598-018-38108-y 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
Habe, Koji
Wada, Hideo
Higashiyama, Ayaka
Akeda, Tomoko
Tsuda, Kenshiro
Mori, Ryoko
Kakeda, Masato
Yamanaka, Keiichi
Mizutani, Hitoshi
Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title_full Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title_fullStr Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title_full_unstemmed Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title_short Elevated plasma D-dimer levels in dermatomyositis patients with cutaneous manifestations
title_sort elevated plasma d-dimer levels in dermatomyositis patients with cutaneous manifestations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363793/
https://www.ncbi.nlm.nih.gov/pubmed/30723246
http://dx.doi.org/10.1038/s41598-018-38108-y
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