
Semiquantitative interpretation of anticardiolipin and antiβ2glycoprotein I antibodies measured with various analytical platforms : communication from the ISTH SSC subcommittee on lupus anticoagulant/antiphospholipid antibodies
- Author
- Arne Vandevelde (UGent) , Walid Chayoua, Bas de Laat, Jean‐Christophe Gris, Gary W. Moore, Jacek Musiał, Stéphane Zuily, Denis Wahl and Katrien Devreese (UGent)
- Organization
- 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
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8728596
- 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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