International multi-center evaluation of a novel chemiluminescence assay for the detection of anti-dsDNA antibodies
Open accessAbstract
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 of > 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 ( p < 0.0001) in active SLE (SLEDAI-2K > 4; n = 232; median value 83.0 IU/mL) versus the inactive patients ( n = 573; median value 22.3 IU/mL), and the SLEDAI-2K scoring correlated with their dsDNA antibody levels (Spearman’s rho = 0.44, p < 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.
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For CIA using INOVA Diagnostics, the median diagnostic specificity for SLE is 96.0% (range 89.8-97.7).
“| INOVA Diagnostics | 96.0 [89.8-97.7] | 39.3 [20.0-54.3] | 60, 61, 67 | CIA |”
From Laboratory evaluation of anti-dsDNA antibodies. (2022) · cites this paper as [67]
The Clinical performance section reports 89.8% specificity for the INOVA QUANTA Flash dsDNA CIA, matching the table’s lower bound. The Discussion reports 96.0% from a previous study, but this paper does not establish the cited table’s median of 96.0% or its upper bound of 97.7%. (LLM, conf=0.88)
Experimental — accuracy not yet measuredFor CIA using INOVA Diagnostics, the median diagnostic sensitivity for SLE is 39.3% (range 20.0-54.3).
“| INOVA Diagnostics | 96.0 [89.8-97.7] | 39.3 [20.0-54.3] | 60, 61, 67 | CIA |”
From Laboratory evaluation of anti-dsDNA antibodies. (2022) · cites this paper as [67]
The Clinical performance section reports 54.3% sensitivity for the INOVA chemiluminescence assay in this study, and the Discussion reports 39.3% from an Italian study. Our copy does not establish 39.3% as the median across studies or document the 20.0% lower end of the cited range. Page numbers were not provided. (LLM, conf=0.88)
Experimental — accuracy not yet measuredThe specificities reported for CIA from INOVA Diagnostics were higher than those reported from DiaSorin, while the reported sensitivities for CIA from DiaSorin were higher than those reported from INOVA.
“The specificities reported for CIA from INOVA Diagnostics (3 studies: 89.8%, 96.0%, 97.7% [60], [61], [67]) were higher than those reported from DiaSorin (2 studies: 82.9%, 84.9% [39], [47]), while the reported sensitivities for CIA from DiaSorin (78.6%, 84.6%) were higher than those reported from INOVA (20%, 39.9%, 54.3%) (Table 2).”
From Laboratory evaluation of anti-dsDNA antibodies. (2022) · cites this paper as [67]
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References 32 · Cited by 37
- Authors
- Bentow, C., Lakos, G., Martis, P., Wahl, E., Garcia, M., Viñas, O., Espinosa, G., Cervera, R., Sjöwall, C., Carmona-Fernandes, D., Santos, M. J., Hanly, J. G., & Mahler, M.
- Affiliations
- Department of Research, Inova Diagnostics, San Diego, CA, USA
- Immunology Department, Centre Diagnostic Biomedic CDB, Hospital Clinic Barcelona, Barcelona, Spain
- Hospital Clínic de Barcelona (ES)
- Linköping University (SE)
- University of Lisbon (PT)
- Dalhousie University (CA)
- ORCID
- Venue
- Lupus
- Publisher
- SAGE Publications
- Published
- 2016-05-31
- Volume
- 25
- Issue
- 8
- Pages
- 864-872
- ISSN
- 0961-2033 (ISSN-L)
- 1477-0962
- OpenAlex
- W2418607842
- Semantic Scholar
- c5f1b4ca6aa616745c79f67009777edfa8e19f41
- Cited by
- 37
- References
- 32
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 3 · 2021: 8 · 2020: 3 · 2019: 4 · 2018: 5 · 2017: 4
- FWCI
- 4.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Lupus (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Health Sciences › Medicine › Pathology and Forensic Medicine › Systemic Sclerosis and Related Diseases
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Vasculitis and related conditions
- Keywords
- anti-dsDNA antibodies, systemic lupus erythematosus, chemiluminescence immunoassay, SLEDAI-2K, disease activity monitoring, ELISA comparison, sensitivity and specificity, autoantibody quantification
- MeSH terms
- Adult, Antibodies, Antinuclear, Canada, DNA, Enzyme-Linked Immunosorbent Assay, Female, Humans, Luminescent Measurements, Lupus Erythematosus, Systemic, Male, Middle Aged, Portugal, Sensitivity and Specificity, Spain, Sweden, United States
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