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Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management

Interstitial lung disease (ILD) is a challenging clinical entity associated with multiple connective tissue diseases, and is a significant cause of morbidity and mortality. Effective therapies for connective tissue disease-associated interstitial lung disease (CTD-ILD) are still lacking. Multidiscip...

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Detalles Bibliográficos
Autores principales: Castelino, Flavia V, Varga, John
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945045/
https://www.ncbi.nlm.nih.gov/pubmed/20735863
http://dx.doi.org/10.1186/ar3097
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author Castelino, Flavia V
Varga, John
author_facet Castelino, Flavia V
Varga, John
author_sort Castelino, Flavia V
collection PubMed
description Interstitial lung disease (ILD) is a challenging clinical entity associated with multiple connective tissue diseases, and is a significant cause of morbidity and mortality. Effective therapies for connective tissue disease-associated interstitial lung disease (CTD-ILD) are still lacking. Multidisciplinary clinics dedicated to the early diagnosis and improved management of patients with CTD-ILD are now being established. There is rapid progress in understanding and identifying the effector cells, the proinflammatory and profibrotic mediators, and the pathways involved in the pathogenesis of CTD-ILD. Serum biomarkers may provide new insights as risk factors for pulmonary fibrosis and as measures of disease progression. Despite these recent advances, the management of patients with CTD-ILD remains suboptimal. Further studies are therefore urgently needed to better understand these conditions, and to develop effective therapeutic interventions.
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spelling pubmed-29450452011-02-23 Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management Castelino, Flavia V Varga, John Arthritis Res Ther Review Interstitial lung disease (ILD) is a challenging clinical entity associated with multiple connective tissue diseases, and is a significant cause of morbidity and mortality. Effective therapies for connective tissue disease-associated interstitial lung disease (CTD-ILD) are still lacking. Multidisciplinary clinics dedicated to the early diagnosis and improved management of patients with CTD-ILD are now being established. There is rapid progress in understanding and identifying the effector cells, the proinflammatory and profibrotic mediators, and the pathways involved in the pathogenesis of CTD-ILD. Serum biomarkers may provide new insights as risk factors for pulmonary fibrosis and as measures of disease progression. Despite these recent advances, the management of patients with CTD-ILD remains suboptimal. Further studies are therefore urgently needed to better understand these conditions, and to develop effective therapeutic interventions. BioMed Central 2010 2010-08-23 /pmc/articles/PMC2945045/ /pubmed/20735863 http://dx.doi.org/10.1186/ar3097 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Review
Castelino, Flavia V
Varga, John
Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title_full Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title_fullStr Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title_full_unstemmed Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title_short Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
title_sort interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945045/
https://www.ncbi.nlm.nih.gov/pubmed/20735863
http://dx.doi.org/10.1186/ar3097
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