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“Mixed connective tissue disease”: a condition in search of an identity

Mixed connective tissue disease was first described as a new autoimmune rheumatic disease in 1972 based on the claim of a distinct clinical picture associated with anti-RNP antibody positivity. Subsequently, this new entity has divided opinions in the rheumatology community. We have reviewed recent...

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Autores principales: Alves, Marta R., Isenberg, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181542/
https://www.ncbi.nlm.nih.gov/pubmed/32130548
http://dx.doi.org/10.1007/s10238-020-00606-7
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author Alves, Marta R.
Isenberg, David A.
author_facet Alves, Marta R.
Isenberg, David A.
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description Mixed connective tissue disease was first described as a new autoimmune rheumatic disease in 1972 based on the claim of a distinct clinical picture associated with anti-RNP antibody positivity. Subsequently, this new entity has divided opinions in the rheumatology community. We have reviewed recent cohort studies with more than 100 patients, comparing the clinical and immunological features, treatment, prognosis and evolution to well-defined autoimmune rheumatic diseases. We also reviewed clinical features of undifferentiated autoimmune rheumatic diseases based on the most recent studies. After gathering and reviewing these data, we discuss whether the designation “mixed connective tissue disease” should be maintained.
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spelling pubmed-71815422020-04-29 “Mixed connective tissue disease”: a condition in search of an identity Alves, Marta R. Isenberg, David A. Clin Exp Med Review Article Mixed connective tissue disease was first described as a new autoimmune rheumatic disease in 1972 based on the claim of a distinct clinical picture associated with anti-RNP antibody positivity. Subsequently, this new entity has divided opinions in the rheumatology community. We have reviewed recent cohort studies with more than 100 patients, comparing the clinical and immunological features, treatment, prognosis and evolution to well-defined autoimmune rheumatic diseases. We also reviewed clinical features of undifferentiated autoimmune rheumatic diseases based on the most recent studies. After gathering and reviewing these data, we discuss whether the designation “mixed connective tissue disease” should be maintained. Springer International Publishing 2020-03-04 2020 /pmc/articles/PMC7181542/ /pubmed/32130548 http://dx.doi.org/10.1007/s10238-020-00606-7 Text en © The Author(s) 2020 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/.
spellingShingle Review Article
Alves, Marta R.
Isenberg, David A.
“Mixed connective tissue disease”: a condition in search of an identity
title “Mixed connective tissue disease”: a condition in search of an identity
title_full “Mixed connective tissue disease”: a condition in search of an identity
title_fullStr “Mixed connective tissue disease”: a condition in search of an identity
title_full_unstemmed “Mixed connective tissue disease”: a condition in search of an identity
title_short “Mixed connective tissue disease”: a condition in search of an identity
title_sort “mixed connective tissue disease”: a condition in search of an identity
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181542/
https://www.ncbi.nlm.nih.gov/pubmed/32130548
http://dx.doi.org/10.1007/s10238-020-00606-7
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