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International multi-center evaluation of a novel chemiluminescence assay for the detection of anti-dsDNA antibodies

Bentow, C. (författare)
Inova Diagnost, CA USA
Lakos, G. (författare)
Inova Diagnost, CA USA
Martis, P. (författare)
Inova Diagnost, CA USA
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Wahl, E. (författare)
Inova Diagnost, CA USA
Garcia, M. (författare)
Hospital Clin Barcelona, Spain
Vinas, O. (författare)
Hospital Clin Barcelona, Spain
Espinosa, G. (författare)
Hospital Clin Barcelona, Spain
Cervera, R. (författare)
Hospital Clin Barcelona, Spain
Sjöwall, Christopher (författare)
Linköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten,Region Östergötland, Reumatologiska kliniken i Östergötland
Carmona-Fernandes, D. (författare)
University of Lisbon, Portugal
Santos, M. J. (författare)
University of Lisbon, Portugal
Hanly, J. G. (författare)
Dalhousie University, Canada
Mahler, M. (författare)
Inova Diagnost, CA USA
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 (creator_code:org_t)
2016-05-31
2016
Engelska.
Ingår i: Lupus. - : SAGE PUBLICATIONS LTD. - 0961-2033 .- 1477-0962. ; 25:8, s. 864-872
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objective: Anti-double stranded desoxyribonucleic acid (anti-dsDNA) antibodies are considered fairly specific for systemic lupus erythematosus (SLE) and their quantification is useful for the clinical management of SLE patients. We assessed the diagnostic performance of the QUANTA Flash dsDNA chemiluminescent immunoassay (CIA) in comparison to an ELISA, using patients from five participating countries. The main focus was to evaluate the correlation between anti-dsDNA antibody results from the CIA and global SLE disease activity, as measured by the SLE Disease Activity Index 2000 (SLEDAI-2K). Patients and methods: A total of 1431 samples (SLE, n=843; disease controls, n=588) from five countries (Canada, USA, Portugal, Sweden and Spain) were tested with QUANTA Flash dsDNA (Inova Diagnostics, San Diego, CA, USA). Data obtained with the QUANTA Lite dsDNA SC ELISA (Inova Diagnostics) were available for samples from three sites (Canada, USA and Sweden, n=566). The SLEDAI-2K scores were available for 805 SLE patients and a cut-off ofamp;gt;4 was used to define active disease. Results: QUANTA Flash dsDNA had a sensitivity of 54.3% for the diagnosis of SLE, combined with 89.8% specificity. Anti-dsDNA antibody levels were significantly higher (pamp;lt;0.0001) in active SLE (SLEDAI-2Kamp;gt;4; n=232; median value 83.0IU/mL) versus the inactive patients (n=573; median value 22.3IU/mL), and the SLEDAI-2K scoring correlated with their dsDNA antibody levels (Spearmans rho=0.44, pamp;lt;0.0001). Similar but less pronounced findings were also found for the ELISA, in relation to disease activity. Conclusions: The QUANTA Flash dsDNA assay showed good clinical performance in a large international multi-center study. Additionally, the strong correlation between anti-dsDNA antibody results and SLEDAI-2K scores supported the potential utility of QUANTA Flash dsDNA for monitoring disease activity.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

anti-dsDNA antibodies; autoantibodies; autoimmune disease; comparative study; diagnostic test; immunoassay; lupus; multicenter study; systemic lupus erythematosus

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