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Interstitial lung disease in Primary Sjögren's syndrome
BACKGROUND: Interstitial lung disease (ILD) may cause life-threatening complications of primary Sjogren’s syndrome (pSS), and has a poor prognosis in terms of survival and quality of life. To date, few studies have investigated the risk factors for ILD detected by high-resolution computed tomography...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882286/ https://www.ncbi.nlm.nih.gov/pubmed/35220958 http://dx.doi.org/10.1186/s12890-022-01868-5 |
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author | Lin, Wei Xin, Zhifei Zhang, Jianlong Liu, Ning Ren, Xiuying Liu, Meilu Su, Yashuang Liu, Yixuan Yang, Liu Guo, Shaoying Yang, Yupeng Li, Yang Cao, Jingjing Ning, Xiaoran Li, Jingjing Xue, He Niu, Nannan Chen, Yingmin Li, Fang Sun, Lijun Zhang, Xiaopeng Zhang, Fengxiao Zhang, Wen |
author_facet | Lin, Wei Xin, Zhifei Zhang, Jianlong Liu, Ning Ren, Xiuying Liu, Meilu Su, Yashuang Liu, Yixuan Yang, Liu Guo, Shaoying Yang, Yupeng Li, Yang Cao, Jingjing Ning, Xiaoran Li, Jingjing Xue, He Niu, Nannan Chen, Yingmin Li, Fang Sun, Lijun Zhang, Xiaopeng Zhang, Fengxiao Zhang, Wen |
author_sort | Lin, Wei |
collection | PubMed |
description | BACKGROUND: Interstitial lung disease (ILD) may cause life-threatening complications of primary Sjogren’s syndrome (pSS), and has a poor prognosis in terms of survival and quality of life. To date, few studies have investigated the risk factors for ILD detected by high-resolution computed tomography (HRCT) in pSS patients with or without respiratory symptoms. METHODS: Data of 333 patients with newly diagnosed pSS were retrospectively analysed. Interstitial lung disease involvement was defined as typical abnormalities on HRCT and/or pulmonary function tests. Multivariate regression model was used to evaluate the association between interstitial lung disease and pSS characteristics. RESULTS: Sixty-six patients (19.82%) were diagnosed with pSS-ILD. Ground glass opacities (87.88%) and septal/sub pleural lines (81.82%) were most frequent. Based on pulmonary high-resolution computed tomography, patients were divided into nonspecific (n = 42), usual (n = 20), lymphocytic interstitial pneumonia (n = 3) and cryptogenic organising pneumonia (n = 1) groups. There was a strong association between erythrocyte sedimentation rate (ESR)/C-reactive protein (CRP) and the HRCT-score. Pulmonary function tests revealed impaired diffusion capacity for carbon monoxide and total lung capacity, and coexistence of small airway lesions in pSS-interstitial lung disease. On logistic regression analysis, age, Raynaud’s phenomenon, lymphopenia, cough, dyspnoea and rampant dental caries were risk factors associated with pSS-interstitial lung disease. CONCLUSIONS: Interstitial lung disease involvement in pSS is a common clinical occurrence. The clinical manifestation is nonspecific and variable; Raynaud’s phenomenon and lymphopenia may predict its onset. pSS patients with advanced age, dry cough and dyspnoea should be systematically evaluated for ILD involvement and managed according to their symptoms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-022-01868-5. |
format | Online Article Text |
id | pubmed-8882286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88822862022-02-28 Interstitial lung disease in Primary Sjögren's syndrome Lin, Wei Xin, Zhifei Zhang, Jianlong Liu, Ning Ren, Xiuying Liu, Meilu Su, Yashuang Liu, Yixuan Yang, Liu Guo, Shaoying Yang, Yupeng Li, Yang Cao, Jingjing Ning, Xiaoran Li, Jingjing Xue, He Niu, Nannan Chen, Yingmin Li, Fang Sun, Lijun Zhang, Xiaopeng Zhang, Fengxiao Zhang, Wen BMC Pulm Med Research BACKGROUND: Interstitial lung disease (ILD) may cause life-threatening complications of primary Sjogren’s syndrome (pSS), and has a poor prognosis in terms of survival and quality of life. To date, few studies have investigated the risk factors for ILD detected by high-resolution computed tomography (HRCT) in pSS patients with or without respiratory symptoms. METHODS: Data of 333 patients with newly diagnosed pSS were retrospectively analysed. Interstitial lung disease involvement was defined as typical abnormalities on HRCT and/or pulmonary function tests. Multivariate regression model was used to evaluate the association between interstitial lung disease and pSS characteristics. RESULTS: Sixty-six patients (19.82%) were diagnosed with pSS-ILD. Ground glass opacities (87.88%) and septal/sub pleural lines (81.82%) were most frequent. Based on pulmonary high-resolution computed tomography, patients were divided into nonspecific (n = 42), usual (n = 20), lymphocytic interstitial pneumonia (n = 3) and cryptogenic organising pneumonia (n = 1) groups. There was a strong association between erythrocyte sedimentation rate (ESR)/C-reactive protein (CRP) and the HRCT-score. Pulmonary function tests revealed impaired diffusion capacity for carbon monoxide and total lung capacity, and coexistence of small airway lesions in pSS-interstitial lung disease. On logistic regression analysis, age, Raynaud’s phenomenon, lymphopenia, cough, dyspnoea and rampant dental caries were risk factors associated with pSS-interstitial lung disease. CONCLUSIONS: Interstitial lung disease involvement in pSS is a common clinical occurrence. The clinical manifestation is nonspecific and variable; Raynaud’s phenomenon and lymphopenia may predict its onset. pSS patients with advanced age, dry cough and dyspnoea should be systematically evaluated for ILD involvement and managed according to their symptoms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-022-01868-5. BioMed Central 2022-02-27 /pmc/articles/PMC8882286/ /pubmed/35220958 http://dx.doi.org/10.1186/s12890-022-01868-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lin, Wei Xin, Zhifei Zhang, Jianlong Liu, Ning Ren, Xiuying Liu, Meilu Su, Yashuang Liu, Yixuan Yang, Liu Guo, Shaoying Yang, Yupeng Li, Yang Cao, Jingjing Ning, Xiaoran Li, Jingjing Xue, He Niu, Nannan Chen, Yingmin Li, Fang Sun, Lijun Zhang, Xiaopeng Zhang, Fengxiao Zhang, Wen Interstitial lung disease in Primary Sjögren's syndrome |
title | Interstitial lung disease in Primary Sjögren's syndrome |
title_full | Interstitial lung disease in Primary Sjögren's syndrome |
title_fullStr | Interstitial lung disease in Primary Sjögren's syndrome |
title_full_unstemmed | Interstitial lung disease in Primary Sjögren's syndrome |
title_short | Interstitial lung disease in Primary Sjögren's syndrome |
title_sort | interstitial lung disease in primary sjögren's syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8882286/ https://www.ncbi.nlm.nih.gov/pubmed/35220958 http://dx.doi.org/10.1186/s12890-022-01868-5 |
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