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Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study

Despite anti-dsDNA antibodies constitute a wide range of specificities, they are considered as the hallmark for systemic lupus erythematosus (SLE). OBJECTIVE: To identify clinical phenotypes associated with anti-dsDNA antibodies, independently of any clinical diagnoses. METHODS: Patients with recent...

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Autores principales: Compagno, Michele, Rekvig, Ole P, Bengtsson, Anders A, Sturfelt, Gunnar, Heegaard, Niels H H, Jönsen, Andreas, Jacobsen, Rasmus Sleimann, Eilertsen, Gro Ø, Fenton, Christopher G, Truedsson, Lennart, Nossent, Johannes C, Jacobsen, Søren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225731/
https://www.ncbi.nlm.nih.gov/pubmed/25396058
http://dx.doi.org/10.1136/lupus-2013-000007
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author Compagno, Michele
Rekvig, Ole P
Bengtsson, Anders A
Sturfelt, Gunnar
Heegaard, Niels H H
Jönsen, Andreas
Jacobsen, Rasmus Sleimann
Eilertsen, Gro Ø
Fenton, Christopher G
Truedsson, Lennart
Nossent, Johannes C
Jacobsen, Søren
author_facet Compagno, Michele
Rekvig, Ole P
Bengtsson, Anders A
Sturfelt, Gunnar
Heegaard, Niels H H
Jönsen, Andreas
Jacobsen, Rasmus Sleimann
Eilertsen, Gro Ø
Fenton, Christopher G
Truedsson, Lennart
Nossent, Johannes C
Jacobsen, Søren
author_sort Compagno, Michele
collection PubMed
description Despite anti-dsDNA antibodies constitute a wide range of specificities, they are considered as the hallmark for systemic lupus erythematosus (SLE). OBJECTIVE: To identify clinical phenotypes associated with anti-dsDNA antibodies, independently of any clinical diagnoses. METHODS: Patients with recent onset of any rheumatic symptoms were screened for antinuclear antibodies (ANA). All ANA-positive and matching ANA-negative patients were examined, and their clinical phenotypes were registered, using a systematic chart formulated after consensus between the participating centres. All patients were tested for different anti-dsDNA antibody specificities with assays habitually used in each participating laboratory. Crithidia Luciliae Immuno Fluorescence Test (CLIFT) was performed three times (with two different commercial kits); solid and solution phase ELISA were performed four times. Associations between clinical phenotypes and results of anti-dsDNA assays were evaluated by linear regression analysis (LRA) and principal component analysis (PCA). RESULTS: Totally, 292 ANA-positive and 292 matching ANA-negative patients were included in the study. A full dataset for statistical analysis was obtained in 547 patients. Anti-dsDNA antibodies were most frequently detected by ELISA. LRA showed that overall positivity of anti-dsDNA antibodies was associated with proteinuria and pleuritis. Alopecia was significantly associated only with CLIFT-positivity. Besides confirming the same findings, PCA showed that combined positivity of CLIFT and ELISA was also associated with lymphopenia. CONCLUSIONS: Our results show that different anti-dsDNA antibody specificities are associated with nephropathy, pleuritis, alopecia and lymphopenia, regardless of the diagnosis. It may challenge the importance of anti-dsDNA antibodies as a diagnostic hallmark for SLE.
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spelling pubmed-42257312014-11-13 Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study Compagno, Michele Rekvig, Ole P Bengtsson, Anders A Sturfelt, Gunnar Heegaard, Niels H H Jönsen, Andreas Jacobsen, Rasmus Sleimann Eilertsen, Gro Ø Fenton, Christopher G Truedsson, Lennart Nossent, Johannes C Jacobsen, Søren Lupus Sci Med Biomarker Studies Despite anti-dsDNA antibodies constitute a wide range of specificities, they are considered as the hallmark for systemic lupus erythematosus (SLE). OBJECTIVE: To identify clinical phenotypes associated with anti-dsDNA antibodies, independently of any clinical diagnoses. METHODS: Patients with recent onset of any rheumatic symptoms were screened for antinuclear antibodies (ANA). All ANA-positive and matching ANA-negative patients were examined, and their clinical phenotypes were registered, using a systematic chart formulated after consensus between the participating centres. All patients were tested for different anti-dsDNA antibody specificities with assays habitually used in each participating laboratory. Crithidia Luciliae Immuno Fluorescence Test (CLIFT) was performed three times (with two different commercial kits); solid and solution phase ELISA were performed four times. Associations between clinical phenotypes and results of anti-dsDNA assays were evaluated by linear regression analysis (LRA) and principal component analysis (PCA). RESULTS: Totally, 292 ANA-positive and 292 matching ANA-negative patients were included in the study. A full dataset for statistical analysis was obtained in 547 patients. Anti-dsDNA antibodies were most frequently detected by ELISA. LRA showed that overall positivity of anti-dsDNA antibodies was associated with proteinuria and pleuritis. Alopecia was significantly associated only with CLIFT-positivity. Besides confirming the same findings, PCA showed that combined positivity of CLIFT and ELISA was also associated with lymphopenia. CONCLUSIONS: Our results show that different anti-dsDNA antibody specificities are associated with nephropathy, pleuritis, alopecia and lymphopenia, regardless of the diagnosis. It may challenge the importance of anti-dsDNA antibodies as a diagnostic hallmark for SLE. BMJ Publishing Group 2014-04-01 /pmc/articles/PMC4225731/ /pubmed/25396058 http://dx.doi.org/10.1136/lupus-2013-000007 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Biomarker Studies
Compagno, Michele
Rekvig, Ole P
Bengtsson, Anders A
Sturfelt, Gunnar
Heegaard, Niels H H
Jönsen, Andreas
Jacobsen, Rasmus Sleimann
Eilertsen, Gro Ø
Fenton, Christopher G
Truedsson, Lennart
Nossent, Johannes C
Jacobsen, Søren
Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title_full Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title_fullStr Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title_full_unstemmed Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title_short Clinical phenotype associations with various types of anti-dsDNA antibodies in patients with recent onset of rheumatic symptoms. Results from a multicentre observational study
title_sort clinical phenotype associations with various types of anti-dsdna antibodies in patients with recent onset of rheumatic symptoms. results from a multicentre observational study
topic Biomarker Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225731/
https://www.ncbi.nlm.nih.gov/pubmed/25396058
http://dx.doi.org/10.1136/lupus-2013-000007
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