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Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis

OBJECTIVE: Dermatomyositis (DM) is a heterogeneous disease with a wide range of clinical manifestations. The aim of the present study was to identify the clinical subtypes of DM by applying cluster analysis. METHODS: We retrospectively reviewed the medical records of 720 DM patients and selected 21...

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Autores principales: Zhu, Huiyi, Wu, Chanyuan, Jiang, Nan, Wang, Yanhong, Zhao, Jiuliang, Xu, Dong, Wang, Qian, Li, Mengtao, Zeng, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771972/
https://www.ncbi.nlm.nih.gov/pubmed/31179648
http://dx.doi.org/10.1111/1756-185X.13609
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author Zhu, Huiyi
Wu, Chanyuan
Jiang, Nan
Wang, Yanhong
Zhao, Jiuliang
Xu, Dong
Wang, Qian
Li, Mengtao
Zeng, Xiaofeng
author_facet Zhu, Huiyi
Wu, Chanyuan
Jiang, Nan
Wang, Yanhong
Zhao, Jiuliang
Xu, Dong
Wang, Qian
Li, Mengtao
Zeng, Xiaofeng
author_sort Zhu, Huiyi
collection PubMed
description OBJECTIVE: Dermatomyositis (DM) is a heterogeneous disease with a wide range of clinical manifestations. The aim of the present study was to identify the clinical subtypes of DM by applying cluster analysis. METHODS: We retrospectively reviewed the medical records of 720 DM patients and selected 21 variables for analysis, including clinical characteristics, laboratory findings, and comorbidities. Principal component analysis (PCA) was first conducted to transform the 21 variables into independent principal components. Patient classification was then performed using cluster analysis based on the PCA‐transformed data. The relationships among the clinical variables were also assessed. RESULTS: We transformed the 21 clinical variables into nine independent principal components by PCA and identified six distinct subgroups. Cluster A was composed of two sub‐clusters of patients with classical DM and classical DM with minimal organ involvement. Cluster B patients were older and had malignancies. Cluster C was characterized by interstitial lung disease (ILD), skin ulcers, and minimal muscle involvement. Cluster D included patients with prominent lung, muscle, and skin involvement. Cluster E contained DM patients with other connective tissue diseases. Cluster F included all patients with myocarditis and prominent myositis and ILD. We found significant differences in treatment across the six clusters, with clusters E, C and D being more likely to receive aggressive immunosuppressive therapy. CONCLUSION: We applied cluster analysis to a large group of DM patients and identified 6 clinical subgroups, underscoring the need for better phenotypic characterization to help develop individualized treatments and improve prognosis.
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spelling pubmed-67719722019-10-07 Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis Zhu, Huiyi Wu, Chanyuan Jiang, Nan Wang, Yanhong Zhao, Jiuliang Xu, Dong Wang, Qian Li, Mengtao Zeng, Xiaofeng Int J Rheum Dis Original Articles OBJECTIVE: Dermatomyositis (DM) is a heterogeneous disease with a wide range of clinical manifestations. The aim of the present study was to identify the clinical subtypes of DM by applying cluster analysis. METHODS: We retrospectively reviewed the medical records of 720 DM patients and selected 21 variables for analysis, including clinical characteristics, laboratory findings, and comorbidities. Principal component analysis (PCA) was first conducted to transform the 21 variables into independent principal components. Patient classification was then performed using cluster analysis based on the PCA‐transformed data. The relationships among the clinical variables were also assessed. RESULTS: We transformed the 21 clinical variables into nine independent principal components by PCA and identified six distinct subgroups. Cluster A was composed of two sub‐clusters of patients with classical DM and classical DM with minimal organ involvement. Cluster B patients were older and had malignancies. Cluster C was characterized by interstitial lung disease (ILD), skin ulcers, and minimal muscle involvement. Cluster D included patients with prominent lung, muscle, and skin involvement. Cluster E contained DM patients with other connective tissue diseases. Cluster F included all patients with myocarditis and prominent myositis and ILD. We found significant differences in treatment across the six clusters, with clusters E, C and D being more likely to receive aggressive immunosuppressive therapy. CONCLUSION: We applied cluster analysis to a large group of DM patients and identified 6 clinical subgroups, underscoring the need for better phenotypic characterization to help develop individualized treatments and improve prognosis. John Wiley and Sons Inc. 2019-06-09 2019-08 /pmc/articles/PMC6771972/ /pubmed/31179648 http://dx.doi.org/10.1111/1756-185X.13609 Text en © 2019 The Authors International Journal of Rheumatic Diseases published by Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zhu, Huiyi
Wu, Chanyuan
Jiang, Nan
Wang, Yanhong
Zhao, Jiuliang
Xu, Dong
Wang, Qian
Li, Mengtao
Zeng, Xiaofeng
Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title_full Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title_fullStr Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title_full_unstemmed Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title_short Identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
title_sort identification of 6 dermatomyositis subgroups using principal component analysis‐based cluster analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771972/
https://www.ncbi.nlm.nih.gov/pubmed/31179648
http://dx.doi.org/10.1111/1756-185X.13609
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