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Task Force Report on “Criteria” Antiphospholipid Antibody Tests

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Abstract

A Task Force of experts in the Antiphospholipid Syndrome (APS) field met prior to the 13th International Congress on Antiphospholipid Antibodies and addressed a number of critical questions regarding the antiphospholipid antibody (aPL) tests included in current international consensus criteria for the classification of APS (anticardiolipin antibodies (aCL), anti-β2glycoprotein I antibodies (aβ2GPI), and lupus anticoagulant (LA) test, namely, the “criteria” aPL tests). The Task Force was divided into the following three subgroups: (1) aCL and aβ2GPI tests, (2) LA test, and (3) the role of aPL as thrombotic risk factors. Subgroup 1 reviewed and critiqued the current state of aCL/aβ2GPI testing and recommended developing international consensus guidelines for performance of these assays and establishing universal units of measurement for anti-β2GPI. Subgroup 2 reviewed recent guidelines for LA testing published by the International Society of Thrombosis and Haemostasis Standardization Subcommittee (ISTH-SSC) on Lupus Anticoagulants and Phospholipid-dependent Antibodies; the subgroup recommended continued close collaboration with ISTH-SSC to address remaining issues, including the role of TCT and PT in LA testing and the validity of integrated test systems that lack mixing studies. Subgroup 3 emphasized the need for more data on the risks associated with aPL and recommended collaborative studies using existing large, population-based, prospective cohorts with available data on thrombosis and/or pregnancy outcomes. Such studies should include a comprehensive panel of current and newer aPL assays, assess the effect of antibody titer, analyze the risks associated with combinations of aPL, and use state-of-the-art statistical approaches for assessment of risk factors.

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Acknowledgments

In addition to the authors, the members of the Task Force on Criteria Antiphospholipid Antibody Tests” include the following: Phillip G. de Groot, PhD (University Medical Center, Utrecht, The Netherlands), Jeffrey Dlott, MD (Quest Diagnostics Laboratories, Chantilly, VA, USA), Emmanuel Favaloro, PhD (Westmead Hospital,Westmead, NSW, Australia), E. Nigel Harris, MD (University of the West Indies. Office of the Vice Chancellor. University of the West Indies. Kingston, Jamaica, WI), Gabriella Lakos, MD, PhD (INOVA Diagnostics Inc. San Diego, CA) Pier Luigi Meroni, MD (Ist G. Pini and Istituto Auxologico Italiano, Milan, Italy), Thomas Ortel, MD (Duke University Medical Center, Durham, NC, USA), Kotaro Otomo, MD (Hokkaido University Graduate School of Medicine, Sapporo, Japan); Vittorio Pengo, MD (University of Padova, Padova, Italy), Angela Tincani, MD (Universty of Brescia, Italy), and Richard Wong, MD (Royal Brisbane and Women’s Hospital, Queensland, Australia). Conflict of InterestSilvia Pierangeli and E. Nigel Harris are co-owners of Louisville APL Diagnostics, Inc. Gabriella Lakos is an employee of INOVA Diagnostics Inc.

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Correspondence to Robert A. S. Roubey MD .

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Roubey, R.A.S., Pierangeli, S.S. (2012). Task Force Report on “Criteria” Antiphospholipid Antibody Tests. In: Erkan, D., Pierangeli, S. (eds) Antiphospholipid Syndrome. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-3194-7_7

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