| Literature DB >> 31401900 |
Valentina Grossi1, Maria Infantino1, Maurizio Benucci2, Francesca Li Gobbi2, Francesca Bandinelli2, Arianna Damiani2, Caterina Bodio3, Maria Orietta Borghi3,4, Michael Mahler5, Mary Ann Aure5, Chelsea Bentow5, Mariangela Manfredi1.
Abstract
In the present study, we evaluated two novel technologies, the chemiluminescent immunoassay (CIA) QUANTA Flash on BIO-FLASH (Inova Diagnostics, San Diego, CA, USA) and the addressable laser bead immunoassay (ALBIA) on BioPlex™ 2200 (Bio-Rad, Hercules, CA, USA) for the detection of anti-cardiolipin IgG/IgM (aCL) and anti-β2-glycoprotein IgG/IgM (aβ2GPI) antibodies. The study was performed on 134 samples from consecutive patients (59 males and 75 females, mean age 54 ± 10 years) who consulted a rheumatologist because thrombosis and/or pregnancy complications were present or another immunological disease (Sjogren's syndrome, inflammatory arthritis). Fourteen patients of the total fulfilled 25the Sydney criteria for APS and for these patients previous results of aPLs were available. Sera were tested for aCL and aβ2GPI of IgG and IgM isotypes using CIA (BIO-FLASH) and ALBIA (BioPlex™ 2200). Overall agreement between CIA and ALBIA ranged from 88.1% (aCL IgG) to 97.8% (aβ2GPI IgG). Cohen's kappa coefficient ranged from 0.53 to 0.91, implying moderate to almost perfect agreement. Almost perfect agreement was found between BioPlex™ 2200 and BIO-FLASH aβ2GPI IgG and aCL IgM with Cohen's kappa of 0.91 and 0.88, respectively. On the other hand, moderate agreement was found between BioPlex™ 2200 and BIO-FLASH aCL IgG and β2GPI IgM assays with Cohen's kappa of 0.57 and 0.53, respectively. The two novel technologies look promising and comparable but further studies with larger cohorts are needed to contribute to the better understanding of the new aPLs antibodies assays performance.Entities:
Keywords: Anti-cardiolipin; addressable laser bead immunoassay; anti-phospholipid antibodies; anti-β2-glycoprotein I; antiphospholipid syndrome; chemiluminescent immunoassays
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Year: 2019 PMID: 31401900 DOI: 10.1080/08820139.2019.1647233
Source DB: PubMed Journal: Immunol Invest ISSN: 0882-0139 Impact factor: 3.657