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Antinucleosome antibodies as a marker of active proliferative lupus nephritis
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1195862
Author(s) Bigler, Cornelia; López-Trascasa, Margarita; Potlukova, Eliska; Moll, Solange; Danner, Doris; Schaller, Monica; Trendelenburg, Marten
Author(s) at UniBasel Trendelenburg, Marten
Year 2008
Title Antinucleosome antibodies as a marker of active proliferative lupus nephritis
Journal American journal of kidney diseases : the official journal of the National Kidney Foundation
Volume 51
Number 4
Pages / Article-Number 624-9
Mesh terms Adult; Aged; Aged, 80 and over; Autoantibodies, blood; Biomarkers, blood; DNA, immunology; Female; Humans; Lupus Nephritis, blood; Male; Middle Aged; Nucleosomes, immunology; Prospective Studies
Abstract BACKGROUND: Antinucleosome autoantibodies were previously described to be a marker of active lupus nephritis. However, the true prevalence of antinucleosome antibodies at the time of active proliferative lupus nephritis has not been well established. Therefore, the aim of this study is to define the prevalence and diagnostic value of autoantibodies against nucleosomes as a marker for active proliferative lupus nephritis. STUDY DESIGN: Prospective multicenter diagnostic test study. SETTING ; PARTICIPANTS: 35 adult patients with systemic lupus erythematosus (SLE) at the time of the renal biopsy showing active class III or IV lupus nephritis compared with 59 control patients with SLE. INDEX TEST: Levels of antinucleosome antibodies and anti-double-stranded DNA (anti-dsDNA) antibodies. REFERENCE TEST: Kidney biopsy findings of class III or IV lupus nephritis at the time of sampling in a study population versus clinically inactive or no nephritis in a control population. RESULTS: Increased concentrations of antinucleosome antibodies were found in 31 of 35 patients (89%) with active proliferative lupus nephritis compared with 47 of 59 control patients (80%) with SLE. No significant difference between the 2 groups with regard to number of positive patients (P = 0.2) or antibody concentrations (P = 0.2) could be found. The area under the receiver operating characteristic curve as a marker of the accuracy of the test in discriminating between proliferative lupus nephritis and inactive/no nephritis in patients with SLE was 0.581 (95% confidence interval, 0.47 to 0.70; P = 0.2). Increased concentrations of anti-dsDNA antibodies were found in 33 of 35 patients (94.3%) with active proliferative lupus nephritis compared with 49 of 58 control patients (84.5%) with SLE (P = 0.2). In patients with proliferative lupus nephritis, significantly higher titers of anti-dsDNA antibodies were detected compared with control patients with SLE (P > 0.001). The area under the receiver operating characteristic curve in discriminating between proliferative lupus nephritis and inactive/no nephritis in patients with SLE was 0.710 (95% confidence interval, 0.60 to 0.82; P > 0.001). CONCLUSIONS: Antinucleosome antibodies have a high prevalence in patients with severe lupus nephritis. However, our data suggest that determining antinucleosome antibodies is of limited help in the distinction of patients with active proliferative lupus nephritis from patients with SLE without active renal disease.
Publisher Elsevier
ISSN/ISBN 0272-6386 ; 1523-6838
edoc-URL https://edoc.unibas.ch/63154/
Full Text on edoc No
Digital Object Identifier DOI 10.1053/j.ajkd.2007.10.041
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/18371538
ISI-Number WOS:000254874400013
Document type (ISI) Journal Article, Multicenter Study
 
   

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