Cited by 73Systemic Lupus Erythematosus ResearchSystemic Sclerosis and Related DiseasesVasculitis and related conditions

Four Anti-dsDNA Antibody Assays in Relation to Systemic Lupus Erythematosus Disease Specificity and Activity

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Enocsson, Helena, Sjöwall, Christopher, Wirestam, Lina, Dahle, Charlotte, Kastbom, Alf, Rönnelid, Johan, Wetterö, Jonas, Skogh, Thomas·2015·The Journal of Rheumatology

Abstract

Objective.: Analysis of antibodies against dsDNA is an important diagnostic tool for systemic lupus erythematosus (SLE), and changes in anti-dsDNA antibody levels are also used to assess disease activity. Herein, 4 assays were compared with regard to SLE specificity, sensitivity, and association with disease activity variables. Methods.: Cross-sectional sera from 178 patients with SLE, of which 11 were followed consecutively, from a regional Swedish SLE register were analyzed for immunoglobulin G (IgG) anti-dsDNA by bead-based multiplex assay (FIDIS; Theradig), fluoroenzyme-immunoassay (EliA; Phadia/Thermo Fisher Scientific), Crithidia luciliae immunofluorescence test (CLIFT; ImmunoConcepts), and line blot (EUROLINE; Euroimmun). All patients with SLE fulfilled the 1982 American College of Rheumatology and/or the 2012 Systemic Lupus International Collaborating Clinics (SLICC-12) classification criteria. Healthy individuals (n = 100), patients with rheumatoid arthritis (n = 95), and patients with primary Sjögren syndrome (n = 54) served as controls. Results.: CLIFT had the highest SLE specificity (98%) whereas EliA had the highest sensitivity (35%). When cutoff levels for FIDIS, EliA, and EUROLINE were adjusted according to SLICC-12 (i.e., double the reference limit when using ELISA), the specificity and sensitivity of FIDIS was comparable to CLIFT. FIDIS and CLIFT also showed the highest concordance (84%). FIDIS performed best regarding association with disease activity in cross-sectional and consecutive samples. Fisher’s exact test revealed striking differences between methods regarding associations with certain disease phenotypes. Conclusion.: CLIFT remains a good choice for diagnostic purposes, but FIDIS performs equally well when the cutoff is adjusted according to SLICC-12. Based on results from cross-sectional and consecutive analyses, FIDIS can also be recommended to monitor disease activity.

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  • All studies that evaluated correlation with disease activity showed a positive correlation between SLEDAI and anti-dsDNA autoantibody titers measured by bead-based multiplex assay.

    “All studies that evaluated correlation with disease activity showed a positive correlation between SLEDAI and anti-dsDNA autoantibody titers measured by bead-based multiplex assay [48], [52], [59], [64], [75], [76].”

    From Laboratory evaluation of anti-dsDNA antibodies. (2022) · cites this paper as [59]

    The Discussion reports positive correlations between anti-dsDNA levels and some disease-activity variables, but explicitly says these were not recorded for SLEDAI-2K or PGA. FIDIS was the bead-based multiplex assay, so this study does not support the citing sentence’s claim of a positive SLEDAI correlation. Page numbers are unavailable in our copy. (LLM, conf=0.87)

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  • Enocsson et al. compared CLIFT, FEIA, multiplexed immunoassay and line blot at a cutoff that corresponded to a specificity of 98% and found that the multiplexed assay had the highest sensitivity.

    “Enocsson et al. compared CLIFT, FEIA, multiplexed immunoassay and line blot at a cutoff that corresponded to a specificity of 98% and found that the multiplexed assay had the highest sensitivity [59].”

    From Laboratory evaluation of anti-dsDNA antibodies. (2022) · cites this paper as [59]

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References 37 · Cited by 73

Authors
Enocsson, H., Sjöwall, C., Wirestam, L., Dahle, C., Kastbom, A., Rönnelid, J., Wetterö, J., & Skogh, T.
Affiliations
Linköping University (SE)
Venue
The Journal of Rheumatology
Published
2015-02-15
Volume
42
Issue
5
Pages
817-825
ISSN
  • 0315-162X (ISSN-L)
  • 1499-2752
OpenAlex
W2149255315
Cited by
73
References
37
Citations by year
2026: 6 · 2025: 1 · 2024: 5 · 2023: 8 · 2022: 8 · 2021: 11 · 2020: 2 · 2019: 6 · 2018: 6 · 2017: 5 · 2016: 8 · 2015: 7
FWCI
7.28
Type
journal article
Language
en
Open access
Locations
  • The Journal of Rheumatology (publishedVersion)
  • PubMed (publishedVersion)
  • DiVA (Linkoping University) (submittedVersion, other-oa)
Funders
  • Svenska Sällskapet för Medicinsk Forskning
  • Linköpings Universitet
  • Vetenskapsrådet (K2011-68X-20611-04-3)
  • Uppsala Universitet
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, assay comparison, sensitivity and specificity, disease activity monitoring, disease phenotypes
MeSH terms
Adolescent, Adult, Aged, Aged, 80 and over, Cross-Sectional Studies, DNA, Female, Humans, Immunoassay, Lupus Erythematosus, Systemic, Male, Middle Aged, Sensitivity and Specificity, Severity of Illness Index, Young Adult

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