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Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies

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Abstract
Background Anti beta 2glycoprotein I (a beta 2GPI) and anticardiolipin (aCL) IgG/IgM show differences in positive/negative agreement and titers between solid phase platforms. Method-specific semiquantitative categorization of titers could improve and harmonize the interpretation across platforms. Aim To evaluate the traditional 40/80-unit thresholds used for aCL and a beta 2GPI for categorization into moderate/high positivity with different analytical systems, and to compare with alternative thresholds. Material and methods aCL and a beta 2GPI thresholds were calculated for two automated systems (chemiluminescent immunoassay [CLIA] and multiplex flow immunoassay [MFI]) by receiver operating characteristic curve analysis on 1108 patient samples, including patients with and without antiphospholipid syndrome (APS), and confirmed on a second population (n = 279). Alternatively, regression analysis on diluted standard material was applied to identify thresholds. Thresholds were compared to 40/80 threshold measured by an enzyme-linked immunosorbent assay (ELISA). Additionally, likelihood ratios (LR) were calculated. Results Threshold levels of 40/80 units show poor agreement between ELISA and automated platforms for classification into low/moderate/high positivity, especially for aCL/a beta 2GPI IgG. Agreement for semiquantitative interpretation of antiphospholipid antibodies (aPL) IgG between ELISA and CLIA/MFI improves with alternative thresholds. LR for aPL IgG increase for thrombotic and obstetric APS based on 40/80 thresholds for ELISA and adapted thresholds for the other systems, but not for IgM. Conclusion Use of 40/80 units as medium/high thresholds is acceptable for aCL/a beta 2GPI IgG ELISA, but not for CLIA and MFI. Alternative semiquantitative thresholds for non-ELISA platforms can be determined by a clinical approach or by using monoclonal antibodies. Semiquantitative reporting of aPL IgM has less impact on increasing probability for APS.
Keywords
antiphospholipid antibodies, classification, immunoassay, risk, thresholds, ANTIPHOSPHOLIPID ANTIBODIES, CLASSIFICATION CRITERIA, DIAGNOSIS, THROMBOSIS, ASSAY, MULTICENTER, CONSENSUS, GUIDANCE, DEFINE, UPDATE

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Citation

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MLA
Vandevelde, Arne, et al. “Semiquantitative Interpretation of Anticardiolipin and Antiβ2glycoprotein I Antibodies Measured with Various Analytical Platforms : Communication from the ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies.” JOURNAL OF THROMBOSIS AND HAEMOSTASIS, vol. 20, no. 2, 2022, pp. 508–24, doi:10.1111/jth.15585.
APA
Vandevelde, A., Chayoua, W., de Laat, B., Gris, J., Moore, G. W., Musiał, J., … Devreese, K. (2022). Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 20(2), 508–524. https://doi.org/10.1111/jth.15585
Chicago author-date
Vandevelde, Arne, Walid Chayoua, Bas de Laat, Jean‐Christophe Gris, Gary W. Moore, Jacek Musiał, Stéphane Zuily, Denis Wahl, and Katrien Devreese. 2022. “Semiquantitative Interpretation of Anticardiolipin and Antiβ2glycoprotein I Antibodies Measured with Various Analytical Platforms : Communication from the ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies.” JOURNAL OF THROMBOSIS AND HAEMOSTASIS 20 (2): 508–24. https://doi.org/10.1111/jth.15585.
Chicago author-date (all authors)
Vandevelde, Arne, Walid Chayoua, Bas de Laat, Jean‐Christophe Gris, Gary W. Moore, Jacek Musiał, Stéphane Zuily, Denis Wahl, and Katrien Devreese. 2022. “Semiquantitative Interpretation of Anticardiolipin and Antiβ2glycoprotein I Antibodies Measured with Various Analytical Platforms : Communication from the ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies.” JOURNAL OF THROMBOSIS AND HAEMOSTASIS 20 (2): 508–524. doi:10.1111/jth.15585.
Vancouver
1.
Vandevelde A, Chayoua W, de Laat B, Gris J, Moore GW, Musiał J, et al. Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies. JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 2022;20(2):508–24.
IEEE
[1]
A. Vandevelde et al., “Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies,” JOURNAL OF THROMBOSIS AND HAEMOSTASIS, vol. 20, no. 2, pp. 508–524, 2022.
@article{8728596,
  abstract     = {{Background Anti beta 2glycoprotein I (a beta 2GPI) and anticardiolipin (aCL) IgG/IgM show differences in positive/negative agreement and titers between solid phase platforms. Method-specific semiquantitative categorization of titers could improve and harmonize the interpretation across platforms. Aim To evaluate the traditional 40/80-unit thresholds used for aCL and a beta 2GPI for categorization into moderate/high positivity with different analytical systems, and to compare with alternative thresholds. Material and methods aCL and a beta 2GPI thresholds were calculated for two automated systems (chemiluminescent immunoassay [CLIA] and multiplex flow immunoassay [MFI]) by receiver operating characteristic curve analysis on 1108 patient samples, including patients with and without antiphospholipid syndrome (APS), and confirmed on a second population (n = 279). Alternatively, regression analysis on diluted standard material was applied to identify thresholds. Thresholds were compared to 40/80 threshold measured by an enzyme-linked immunosorbent assay (ELISA). Additionally, likelihood ratios (LR) were calculated. Results Threshold levels of 40/80 units show poor agreement between ELISA and automated platforms for classification into low/moderate/high positivity, especially for aCL/a beta 2GPI IgG. Agreement for semiquantitative interpretation of antiphospholipid antibodies (aPL) IgG between ELISA and CLIA/MFI improves with alternative thresholds. LR for aPL IgG increase for thrombotic and obstetric APS based on 40/80 thresholds for ELISA and adapted thresholds for the other systems, but not for IgM. Conclusion Use of 40/80 units as medium/high thresholds is acceptable for aCL/a beta 2GPI IgG ELISA, but not for CLIA and MFI. Alternative semiquantitative thresholds for non-ELISA platforms can be determined by a clinical approach or by using monoclonal antibodies. Semiquantitative reporting of aPL IgM has less impact on increasing probability for APS.}},
  author       = {{Vandevelde, Arne and Chayoua, Walid and de Laat, Bas and Gris, Jean‐Christophe and Moore, Gary W. and Musiał, Jacek and Zuily, Stéphane and Wahl, Denis and Devreese, Katrien}},
  issn         = {{1538-7933}},
  journal      = {{JOURNAL OF THROMBOSIS AND HAEMOSTASIS}},
  keywords     = {{antiphospholipid antibodies,classification,immunoassay,risk,thresholds,ANTIPHOSPHOLIPID ANTIBODIES,CLASSIFICATION CRITERIA,DIAGNOSIS,THROMBOSIS,ASSAY,MULTICENTER,CONSENSUS,GUIDANCE,DEFINE,UPDATE}},
  language     = {{eng}},
  number       = {{2}},
  pages        = {{508--524}},
  title        = {{Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies}},
  url          = {{http://doi.org/10.1111/jth.15585}},
  volume       = {{20}},
  year         = {{2022}},
}

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