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Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis
Galectin 1 (Gal1) is a lectin with a wide cellular expression that functions as a negative regulator of the immune system in several animal models of autoimmune diseases. Identification of patients with rheumatoid arthritis (RA) has improved during the last decade, although there is still a need for...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576119/ https://www.ncbi.nlm.nih.gov/pubmed/33082382 http://dx.doi.org/10.1038/s41598-020-74185-8 |
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author | Triguero-Martínez, Ana de la Fuente, Hortensia Montes, Nuria Ortiz, Ana María Roy-Vallejo, Emilia Castañeda, Santos González-Alvaro, Isidoro Lamana, Amalia |
author_facet | Triguero-Martínez, Ana de la Fuente, Hortensia Montes, Nuria Ortiz, Ana María Roy-Vallejo, Emilia Castañeda, Santos González-Alvaro, Isidoro Lamana, Amalia |
author_sort | Triguero-Martínez, Ana |
collection | PubMed |
description | Galectin 1 (Gal1) is a lectin with a wide cellular expression that functions as a negative regulator of the immune system in several animal models of autoimmune diseases. Identification of patients with rheumatoid arthritis (RA) has improved during the last decade, although there is still a need for biomarkers allowing an early diagnosis. In this regard, it has been recently proposed that Gal1 serum levels are increased in patients with RA compared to the general population. However, this topic is controversial in the literature. In this work, we provide additional information about the potential usefulness of Gal1 serum levels as a biomarker for RA diagnosis. We studied Gal1 serum and synovial fluid levels and clinical parameters in samples from 62 patients with early arthritis belonging to the PEARL study. In addition, 24 healthy donors were studied. We found that both patients fulfilling RA criteria and patients with undifferentiated arthritis showed higher Gal1 levels than healthy donors. Similar findings were observed in synovial fluid, which showed even higher levels than serum. However, we did not find correlation between Gal1 levels and disease activity or disability. Therefore, our results suggest that Gal1 could be a diagnostic but not a severity biomarker. |
format | Online Article Text |
id | pubmed-7576119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75761192020-10-21 Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis Triguero-Martínez, Ana de la Fuente, Hortensia Montes, Nuria Ortiz, Ana María Roy-Vallejo, Emilia Castañeda, Santos González-Alvaro, Isidoro Lamana, Amalia Sci Rep Article Galectin 1 (Gal1) is a lectin with a wide cellular expression that functions as a negative regulator of the immune system in several animal models of autoimmune diseases. Identification of patients with rheumatoid arthritis (RA) has improved during the last decade, although there is still a need for biomarkers allowing an early diagnosis. In this regard, it has been recently proposed that Gal1 serum levels are increased in patients with RA compared to the general population. However, this topic is controversial in the literature. In this work, we provide additional information about the potential usefulness of Gal1 serum levels as a biomarker for RA diagnosis. We studied Gal1 serum and synovial fluid levels and clinical parameters in samples from 62 patients with early arthritis belonging to the PEARL study. In addition, 24 healthy donors were studied. We found that both patients fulfilling RA criteria and patients with undifferentiated arthritis showed higher Gal1 levels than healthy donors. Similar findings were observed in synovial fluid, which showed even higher levels than serum. However, we did not find correlation between Gal1 levels and disease activity or disability. Therefore, our results suggest that Gal1 could be a diagnostic but not a severity biomarker. Nature Publishing Group UK 2020-10-20 /pmc/articles/PMC7576119/ /pubmed/33082382 http://dx.doi.org/10.1038/s41598-020-74185-8 Text en © The Author(s) 2020 Open Access This 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 | Article Triguero-Martínez, Ana de la Fuente, Hortensia Montes, Nuria Ortiz, Ana María Roy-Vallejo, Emilia Castañeda, Santos González-Alvaro, Isidoro Lamana, Amalia Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title | Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title_full | Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title_fullStr | Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title_full_unstemmed | Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title_short | Validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
title_sort | validation of galectin-1 as potential diagnostic biomarker of early rheumatoid arthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576119/ https://www.ncbi.nlm.nih.gov/pubmed/33082382 http://dx.doi.org/10.1038/s41598-020-74185-8 |
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