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Clinical Chemistry and Laboratory Medicine (CCLM)

Published in Association with the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM)

Editor-in-Chief: Plebani, Mario

Ed. by Gillery, Philippe / Lackner, Karl J. / Lippi, Giuseppe / Melichar, Bohuslav / Payne, Deborah A. / Schlattmann, Peter / Tate, Jillian R.

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1437-4331
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Volume 52, Issue 4

Issues

Value-added reporting of antinuclear antibody testing by automated indirect immunofluorescence analysis

Sofie Schouwers / Myriam Bonnet / Patrick Verschueren / René Westhovens / Daniel Blockmans / Godelieve Mariën / Xavier Bossuyt
  • Corresponding author
  • Laboratory Medicine, University Hospitals Leuven and Experimental Laboratory Immunology, Department of Microbiology and Immunology, KU Leuven, Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium
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Published Online: 2013-11-13 | DOI: https://doi.org/10.1515/cclm-2013-0610

Abstract

Background: Automated systems for antinuclear antibody analysis are being introduced. The aim was to evaluate whether automated quantitative reading of fluorescence intensity is clinically relevant and allows for value-added reporting of test results.

Methods: Consecutive samples (n=260) were used to correlate fluorescence intensity with end-point titer. Moreover, 434 samples from controls (150 healthy blood donors, 150 chronic fatigue syndrome, and 134 diseased controls) and 252 samples (obtained at diagnosis) from patients with systemic rheumatic diseases were screened for antinuclear antibodies (1:80) on HEp-2 cells using NOVA View®, and likelihood ratios were calculated for fluorescence intensity result intervals.

Results: There was a significant correlation between end-point titer and fluorescence intensity. Likelihood ratios for a systemic rheumatic disease increased with increasing fluorescence intensity. The likelihood ratio for a systemic rheumatic disease was 0.06, 0.18, 0.51, 5.3, and 37.5 for a fluorescence intensity of ≤66, 67–150, 151–300, 301–1000, >1000, respectively. A range of 31%–37% of the patients with Sjögren’s syndrome, systemic sclerosis or systemic lupus erythematosus had fluorescence intensities >1000.

Conclusions: Estimation of fluorescence intensity by automated antinuclear antibody analysis offers clinically useful information. Likelihood ratios based on fluorescence intensity test result intervals aid with the interpretation of automated antinuclear antibody analysis and allow value-added reporting.

Keywords: antinuclear antibodies; automation; indirect immunofluorescence; likelihood ratio

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About the article

Corresponding author: Xavier Bossuyt, Laboratory Medicine, University Hospitals Leuven and Experimental Laboratory Immunology, Department of Microbiology and Immunology, KU Leuven, Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium, Phone: +32 16 347009, Fax: +32 16 347931, E-mail:


Received: 2013-07-31

Accepted: 2013-10-13

Published Online: 2013-11-13

Published in Print: 2014-04-01


Citation Information: Clinical Chemistry and Laboratory Medicine, Volume 52, Issue 4, Pages 547–551, ISSN (Online) 1437-4331, ISSN (Print) 1434-6621, DOI: https://doi.org/10.1515/cclm-2013-0610.

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