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Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study

Objectives: Anti-pentraxin 3 (PTX3) auto-antibodies were found to be associated with the absence of renal involvement in systemic lupus erythematosus (SLE). This study is to investigate the prevalence of anti-PTX3 auto-antibodies and their clinical significance based on a large Chinese lupus nephrit...

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Autores principales: Yuan, Mo, Tan, Ying, Pang, Yun, Li, Yong-zhe, Song, Yan, Yu, Feng, Zhao, Ming-hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014382/
https://www.ncbi.nlm.nih.gov/pubmed/28393653
http://dx.doi.org/10.1080/0886022X.2017.1308258
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author Yuan, Mo
Tan, Ying
Pang, Yun
Li, Yong-zhe
Song, Yan
Yu, Feng
Zhao, Ming-hui
author_facet Yuan, Mo
Tan, Ying
Pang, Yun
Li, Yong-zhe
Song, Yan
Yu, Feng
Zhao, Ming-hui
author_sort Yuan, Mo
collection PubMed
description Objectives: Anti-pentraxin 3 (PTX3) auto-antibodies were found to be associated with the absence of renal involvement in systemic lupus erythematosus (SLE). This study is to investigate the prevalence of anti-PTX3 auto-antibodies and their clinical significance based on a large Chinese lupus nephritis cohort. Methods: One hundred and ninety-six active lupus nephritis patients, 150 SLE patients without clinical renal involvement, and 100 healthy controls were enrolled. Serum anti-PTX3 auto-antibodies and PTX3 levels were screened by enzyme-linked immunosorbent assay (ELISA). The associations between anti-PTX3 auto-antibodies and clinicopathological parameters in lupus nephritis were further analyzed. Results: Anti-PTX3 auto-antibodies were less prevalent in active lupus nephritis patients compared with SLE without renal involvement (19.4% (38/196) versus 40.7% (61/150), p < .001). The serum levels of anti-PTX3 auto-antibodies were negatively correlated with proteinuria in lupus nephritis (r = −.143, p = .047). The levels of proteinuria, serum creatinine, and the prevalence of thrombotic microangiopathy were significantly higher in patients with higher PTX3 levels (≥3.207 ng/ml) and without anti-PTX3 auto-antibodies compared with patients with lower PTX3 levels (<3.207 ng/ml) and with anti-PTX3 auto-antibodies (4.79 (3.39–8.28) versus 3.95 (1.78–7.0), p = .03; 168.84 ± 153.63 versus 101.44 ± 47.36, p = .01; 34.1% (14/41) versus 0% (0/9), p = .04; respectively). Conclusion: Anti-PTX3 auto-antibodies were less prevalent in active lupus nephritis patients compared with SLE without renal involvement and associated with less severe renal damage, especially with the combined evaluation of serum PTX3 levels.
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spelling pubmed-60143822018-06-28 Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study Yuan, Mo Tan, Ying Pang, Yun Li, Yong-zhe Song, Yan Yu, Feng Zhao, Ming-hui Ren Fail Laboratory Study Objectives: Anti-pentraxin 3 (PTX3) auto-antibodies were found to be associated with the absence of renal involvement in systemic lupus erythematosus (SLE). This study is to investigate the prevalence of anti-PTX3 auto-antibodies and their clinical significance based on a large Chinese lupus nephritis cohort. Methods: One hundred and ninety-six active lupus nephritis patients, 150 SLE patients without clinical renal involvement, and 100 healthy controls were enrolled. Serum anti-PTX3 auto-antibodies and PTX3 levels were screened by enzyme-linked immunosorbent assay (ELISA). The associations between anti-PTX3 auto-antibodies and clinicopathological parameters in lupus nephritis were further analyzed. Results: Anti-PTX3 auto-antibodies were less prevalent in active lupus nephritis patients compared with SLE without renal involvement (19.4% (38/196) versus 40.7% (61/150), p < .001). The serum levels of anti-PTX3 auto-antibodies were negatively correlated with proteinuria in lupus nephritis (r = −.143, p = .047). The levels of proteinuria, serum creatinine, and the prevalence of thrombotic microangiopathy were significantly higher in patients with higher PTX3 levels (≥3.207 ng/ml) and without anti-PTX3 auto-antibodies compared with patients with lower PTX3 levels (<3.207 ng/ml) and with anti-PTX3 auto-antibodies (4.79 (3.39–8.28) versus 3.95 (1.78–7.0), p = .03; 168.84 ± 153.63 versus 101.44 ± 47.36, p = .01; 34.1% (14/41) versus 0% (0/9), p = .04; respectively). Conclusion: Anti-PTX3 auto-antibodies were less prevalent in active lupus nephritis patients compared with SLE without renal involvement and associated with less severe renal damage, especially with the combined evaluation of serum PTX3 levels. Taylor & Francis 2017-04-10 /pmc/articles/PMC6014382/ /pubmed/28393653 http://dx.doi.org/10.1080/0886022X.2017.1308258 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Laboratory Study
Yuan, Mo
Tan, Ying
Pang, Yun
Li, Yong-zhe
Song, Yan
Yu, Feng
Zhao, Ming-hui
Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title_full Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title_fullStr Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title_full_unstemmed Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title_short Anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
title_sort anti-pentraxin 3 auto-antibodies might be protective in lupus nephritis: a large cohort study
topic Laboratory Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014382/
https://www.ncbi.nlm.nih.gov/pubmed/28393653
http://dx.doi.org/10.1080/0886022X.2017.1308258
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