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Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis
PURPOSE OF REVIEW: At the time of diagnosis, systemic sclerosis (SSc) is often well established with significant irreversible tissue and organ damage. Definitions of ‘early SSc’ have been proposed, which include the presence of SSc-associated autoantibodies. In addition, functional autoantibodies th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams And Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029444/ https://www.ncbi.nlm.nih.gov/pubmed/27387266 http://dx.doi.org/10.1097/BOR.0000000000000325 |
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author | Choi, May Y. Fritzler, Marvin J. |
author_facet | Choi, May Y. Fritzler, Marvin J. |
author_sort | Choi, May Y. |
collection | PubMed |
description | PURPOSE OF REVIEW: At the time of diagnosis, systemic sclerosis (SSc) is often well established with significant irreversible tissue and organ damage. Definitions of ‘early SSc’ have been proposed, which include the presence of SSc-associated autoantibodies. In addition, functional autoantibodies that are believed to be involved in SSc pathogenesis need to be considered. In this review, recent advances in the diagnostic utility and pathogenic role of autoantibodies in early SSc are summarized. Moreover, we propose a clinical care pathway illustrating how autoantibody testing along with key clinical features can be used to make an earlier diagnosis of SSc. RECENT FINDINGS: Recent evidence has helped to develop a clearer understanding of the natural history, early clinical features, and autoantibodies that are predictors of SSc. The role of functional autoantibodies is leading to innovative approaches to evidence-based interventions and therapies that are based on mechanisms of disease. SUMMARY: Despite substantial advances, the high morbidity and mortality that currently characterizes SSc can largely be attributed to a delay in diagnosis, gaps in our understanding of the role of autoantibodies in early disease, and limited effective therapeutic options. An early and accurate diagnosis of SSc and use of autoantibody testing embedded in evidence-based clinical care pathways will help improve SSc-associated clinical outcomes and healthcare expenditures. |
format | Online Article Text |
id | pubmed-5029444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams And Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-50294442016-10-04 Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis Choi, May Y. Fritzler, Marvin J. Curr Opin Rheumatol RAYNAUD PHENOMENON, SCLERODERMA, OVERLAP SYNDROMES AND OTHER FIBROSING SYNDROMES: Edited by John Varga PURPOSE OF REVIEW: At the time of diagnosis, systemic sclerosis (SSc) is often well established with significant irreversible tissue and organ damage. Definitions of ‘early SSc’ have been proposed, which include the presence of SSc-associated autoantibodies. In addition, functional autoantibodies that are believed to be involved in SSc pathogenesis need to be considered. In this review, recent advances in the diagnostic utility and pathogenic role of autoantibodies in early SSc are summarized. Moreover, we propose a clinical care pathway illustrating how autoantibody testing along with key clinical features can be used to make an earlier diagnosis of SSc. RECENT FINDINGS: Recent evidence has helped to develop a clearer understanding of the natural history, early clinical features, and autoantibodies that are predictors of SSc. The role of functional autoantibodies is leading to innovative approaches to evidence-based interventions and therapies that are based on mechanisms of disease. SUMMARY: Despite substantial advances, the high morbidity and mortality that currently characterizes SSc can largely be attributed to a delay in diagnosis, gaps in our understanding of the role of autoantibodies in early disease, and limited effective therapeutic options. An early and accurate diagnosis of SSc and use of autoantibody testing embedded in evidence-based clinical care pathways will help improve SSc-associated clinical outcomes and healthcare expenditures. Lippincott Williams And Wilkins 2016-11 2016-09-28 /pmc/articles/PMC5029444/ /pubmed/27387266 http://dx.doi.org/10.1097/BOR.0000000000000325 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | RAYNAUD PHENOMENON, SCLERODERMA, OVERLAP SYNDROMES AND OTHER FIBROSING SYNDROMES: Edited by John Varga Choi, May Y. Fritzler, Marvin J. Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title | Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title_full | Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title_fullStr | Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title_full_unstemmed | Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title_short | Progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
title_sort | progress in understanding the diagnostic and pathogenic role of autoantibodies associated with systemic sclerosis |
topic | RAYNAUD PHENOMENON, SCLERODERMA, OVERLAP SYNDROMES AND OTHER FIBROSING SYNDROMES: Edited by John Varga |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029444/ https://www.ncbi.nlm.nih.gov/pubmed/27387266 http://dx.doi.org/10.1097/BOR.0000000000000325 |
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