Comparison of current methods for anti‐dsDNA antibody detection and reshaping diagnostic strategies

التفاصيل البيبلوغرافية
العنوان: Comparison of current methods for anti‐dsDNA antibody detection and reshaping diagnostic strategies
المؤلفون: Maria Infantino, Boaz Palterer, Giulia Previtali, Maria‐Grazia Alessio, Danilo Villalta, Teresa Carbone, Stefan Platzgummer, Giusi Paura, Caterina Castiglione, Martina Fabris, Giampaola Pesce, Brunetta Porcelli, Lucia Terzuoli, Maria‐Romana Bacarelli, Marilina Tampoia, Luigi Cinquanta, Ignazio Brusca, Francesca Buzzolini, Maurizio Benucci, Matteo Tortora, Lorenzo Tronchin, Valerio Guarrasi, Paolo Soda, Mariangela Manfredi, Nicola Bizzaro
المصدر: Scandinavian Journal of Immunology. 96
بيانات النشر: Wiley, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Sjogren's Syndrome, Antibodies, Antinuclear, Immunology, Humans, Lupus Erythematosus, Systemic, General Medicine, Autoimmune Diseases
الوصف: Anti-double-stranded DNA antibodies (anti-dsDNA) are considered a specific marker for systemic lupus erythematosus (SLE). Though the Farr technique was once the reference method for their detection, it has been almost entirely replaced by more recently developed assays. However, there is still no solid evidence of the commutability of these methods in terms of diagnostic accuracy and their correlation with the Crithidia luciliae immunofluorescence test (CLIFT). Anti-dsDNA antibody levels were measured in 80 subjects: 24 patients with SLE, 36 disease controls drawn from different autoimmune rheumatic diseases (14 systemic sclerosis, 10 Sjögren's syndrome, nine autoimmune myositis, three mixed connective tissue disease), 10 inflammatory arthritis and 10 apparently healthy blood donors by eight different methods: fluorescence enzyme immunoassay, microdot array, chemiluminescent immunoassay (two assays), multiplex flow immunoassay, particle multi-analyte technology immunoassay and two CLIFT. At the recommended manufacturer cut-off, the sensitivity varied from 67% to 92%, while the specificity ranged from 84% to 98%. Positive agreement among CLIFT and the other assays was higher than negative agreement. Mean agreement among methods assessed by the Cohen's kappa was 0.715, ranging from moderate (0.588) to almost perfect (0.888). Evaluation of the concordance among quantitative values by regression analysis showed a poor correlation index (mean r2, 0.66). The present study shows that current technologies for anti-dsDNA antibody detection are not fully comparable. In particular, their different correlation with CLIFT influences their positioning in the diagnostic algorithm for SLE (either in association or sequentially). Considering the high intermethod variability, harmonization and commutability of anti-dsDNA antibody testing remains an unachieved goal.
تدمد: 1365-3083
0300-9475
DOI: 10.1111/sji.13220
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c58cc4e4034b494edeca5af01703666
https://doi.org/10.1111/sji.13220
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....7c58cc4e4034b494edeca5af01703666
قاعدة البيانات: OpenAIRE
الوصف
تدمد:13653083
03009475
DOI:10.1111/sji.13220