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Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease

OBJECTIVE: S100A12 is an emerging inflammatory disease biomarker. Interstitial lung disease (ILD) is a common, severe complication of dermatomyositis (DM). This study was performed to investigate the association between S100A12 and disease activity and prognosis in patients with DM-associated ILD (i...

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Autores principales: Lou, Yueyan, Zheng, Yu, Fan, Bijun, Zhang, Liyan, Zhu, Feng, Wang, Xiaodong, Chen, Zhiwei, Tan, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607057/
https://www.ncbi.nlm.nih.gov/pubmed/31865833
http://dx.doi.org/10.1177/0300060519887841
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author Lou, Yueyan
Zheng, Yu
Fan, Bijun
Zhang, Liyan
Zhu, Feng
Wang, Xiaodong
Chen, Zhiwei
Tan, Xiaoming
author_facet Lou, Yueyan
Zheng, Yu
Fan, Bijun
Zhang, Liyan
Zhu, Feng
Wang, Xiaodong
Chen, Zhiwei
Tan, Xiaoming
author_sort Lou, Yueyan
collection PubMed
description OBJECTIVE: S100A12 is an emerging inflammatory disease biomarker. Interstitial lung disease (ILD) is a common, severe complication of dermatomyositis (DM). This study was performed to investigate the association between S100A12 and disease activity and prognosis in patients with DM-associated ILD (i.e., DM-ILD). METHODS: Serum S100A12 levels were measured using enzyme-linked immunosorbent assays in patients with stable DM-ILD, patients with acute exacerbation of DM-ILD (AE DM-ILD), and healthy controls (HCs). The relationships of serum S100A12 levels with C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), ferritin, high-resolution computed tomography (HRCT) scores, and pulmonary functions were evaluated by multiple unpaired t-tests and Pearson correlation. RESULTS: Serum S100A12 levels were higher in patients with stable DM-ILD and those with AE DM-ILD than in HCs. Serum S100A12 levels in patients with stable DM-ILD and those with AE DM-ILD were positively correlated with CRP, ESR, and ferritin. S100A12 levels were positively correlated with HRCT scores in patients with stable DM-ILD and those with AE DM-ILD, while they were negatively correlated with predicted percentages of forced vital capacity and predicted percentages of carbon monoxide diffusing capacity in those patients. CONCLUSION: Our findings demonstrate the usefulness of serum S100A12 levels for assessing clinical severity and prognosis of DM-ILD.
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spelling pubmed-76070572020-11-12 Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease Lou, Yueyan Zheng, Yu Fan, Bijun Zhang, Liyan Zhu, Feng Wang, Xiaodong Chen, Zhiwei Tan, Xiaoming J Int Med Res Retrospective Clinical Research Report OBJECTIVE: S100A12 is an emerging inflammatory disease biomarker. Interstitial lung disease (ILD) is a common, severe complication of dermatomyositis (DM). This study was performed to investigate the association between S100A12 and disease activity and prognosis in patients with DM-associated ILD (i.e., DM-ILD). METHODS: Serum S100A12 levels were measured using enzyme-linked immunosorbent assays in patients with stable DM-ILD, patients with acute exacerbation of DM-ILD (AE DM-ILD), and healthy controls (HCs). The relationships of serum S100A12 levels with C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), ferritin, high-resolution computed tomography (HRCT) scores, and pulmonary functions were evaluated by multiple unpaired t-tests and Pearson correlation. RESULTS: Serum S100A12 levels were higher in patients with stable DM-ILD and those with AE DM-ILD than in HCs. Serum S100A12 levels in patients with stable DM-ILD and those with AE DM-ILD were positively correlated with CRP, ESR, and ferritin. S100A12 levels were positively correlated with HRCT scores in patients with stable DM-ILD and those with AE DM-ILD, while they were negatively correlated with predicted percentages of forced vital capacity and predicted percentages of carbon monoxide diffusing capacity in those patients. CONCLUSION: Our findings demonstrate the usefulness of serum S100A12 levels for assessing clinical severity and prognosis of DM-ILD. SAGE Publications 2019-12-23 /pmc/articles/PMC7607057/ /pubmed/31865833 http://dx.doi.org/10.1177/0300060519887841 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Lou, Yueyan
Zheng, Yu
Fan, Bijun
Zhang, Liyan
Zhu, Feng
Wang, Xiaodong
Chen, Zhiwei
Tan, Xiaoming
Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title_full Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title_fullStr Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title_full_unstemmed Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title_short Serum S100A12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
title_sort serum s100a12 levels are correlated with clinical severity in patients with dermatomyositis-associated interstitial lung disease
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607057/
https://www.ncbi.nlm.nih.gov/pubmed/31865833
http://dx.doi.org/10.1177/0300060519887841
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