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Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata

BACKGROUND: Alopecia areata (AA), a chronic, relapsing hair-loss disorder, is considered to be a T-cell-mediated autoimmune disease. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cold stress, and has been identified as a damage-associated molecu...

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Autores principales: Shin, Jung-Min, Ko, Jung-Woo, Kwon, In Sun, Choi, Jong-Won, Hong, Dongkyun, Lee, Jin-Hyup, Seo, Young-Joon, Kim, Chang-Deok, Lee, Jeung-Hoon, Lee, Young, Park, Kyung-Duck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992760/
https://www.ncbi.nlm.nih.gov/pubmed/33911616
http://dx.doi.org/10.5021/ad.2019.31.4.387
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author Shin, Jung-Min
Ko, Jung-Woo
Kwon, In Sun
Choi, Jong-Won
Hong, Dongkyun
Lee, Jin-Hyup
Seo, Young-Joon
Kim, Chang-Deok
Lee, Jeung-Hoon
Lee, Young
Park, Kyung-Duck
author_facet Shin, Jung-Min
Ko, Jung-Woo
Kwon, In Sun
Choi, Jong-Won
Hong, Dongkyun
Lee, Jin-Hyup
Seo, Young-Joon
Kim, Chang-Deok
Lee, Jeung-Hoon
Lee, Young
Park, Kyung-Duck
author_sort Shin, Jung-Min
collection PubMed
description BACKGROUND: Alopecia areata (AA), a chronic, relapsing hair-loss disorder, is considered to be a T-cell-mediated autoimmune disease. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cold stress, and has been identified as a damage-associated molecular pattern (DAMP) molecule that triggers the inflammatory response. Recent studies have shown that high-mobility group box 1, another DAMP molecule, is elevated in serum and scalp tissue of AA patients, suggesting a relationship between DAMP molecules and the pathogenesis of AA. OBJECTIVE: To investigate the clinical significance of serum CIRP levels in AA. METHODS: The serum levels of CIRP were compared between 68 patients with AA and 20 healthy controls. Additionally, the correlation between CIRP level and various clinical parameters was evaluated. RESULTS: The serum CIRP levels were significantly higher in AA patients compared to healthy subjects. Moreover, there was an association between the serum CIRP level and clinical characteristics, such as disease duration and disease activity. However, there was no significant difference in the serum CIRP level among the clinical types of AA (AA multiplex, alopecia totalis, and alopecia universalis). CONCLUSION: These results suggest that CIRP may play a significant role in the pathogenesis of AA and could be a potential biologic marker for monitoring the disease activity of AA.
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spelling pubmed-79927602021-04-27 Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata Shin, Jung-Min Ko, Jung-Woo Kwon, In Sun Choi, Jong-Won Hong, Dongkyun Lee, Jin-Hyup Seo, Young-Joon Kim, Chang-Deok Lee, Jeung-Hoon Lee, Young Park, Kyung-Duck Ann Dermatol Original Article BACKGROUND: Alopecia areata (AA), a chronic, relapsing hair-loss disorder, is considered to be a T-cell-mediated autoimmune disease. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cold stress, and has been identified as a damage-associated molecular pattern (DAMP) molecule that triggers the inflammatory response. Recent studies have shown that high-mobility group box 1, another DAMP molecule, is elevated in serum and scalp tissue of AA patients, suggesting a relationship between DAMP molecules and the pathogenesis of AA. OBJECTIVE: To investigate the clinical significance of serum CIRP levels in AA. METHODS: The serum levels of CIRP were compared between 68 patients with AA and 20 healthy controls. Additionally, the correlation between CIRP level and various clinical parameters was evaluated. RESULTS: The serum CIRP levels were significantly higher in AA patients compared to healthy subjects. Moreover, there was an association between the serum CIRP level and clinical characteristics, such as disease duration and disease activity. However, there was no significant difference in the serum CIRP level among the clinical types of AA (AA multiplex, alopecia totalis, and alopecia universalis). CONCLUSION: These results suggest that CIRP may play a significant role in the pathogenesis of AA and could be a potential biologic marker for monitoring the disease activity of AA. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019-08 2019-07-01 /pmc/articles/PMC7992760/ /pubmed/33911616 http://dx.doi.org/10.5021/ad.2019.31.4.387 Text en Copyright © 2019 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shin, Jung-Min
Ko, Jung-Woo
Kwon, In Sun
Choi, Jong-Won
Hong, Dongkyun
Lee, Jin-Hyup
Seo, Young-Joon
Kim, Chang-Deok
Lee, Jeung-Hoon
Lee, Young
Park, Kyung-Duck
Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title_full Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title_fullStr Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title_full_unstemmed Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title_short Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
title_sort clinical relevance for serum cold-inducible rna-binding protein level in alopecia areata
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992760/
https://www.ncbi.nlm.nih.gov/pubmed/33911616
http://dx.doi.org/10.5021/ad.2019.31.4.387
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