Thromb Haemost 2002; 88(01): 66-73
DOI: 10.1055/s-0037-1613156
Review Article
Schattauer GmbH

Inter-laboratory Variability of Anti-β2-glycoprotein I Measurement

A Collaborative Study in the Frame of the European Forum on Antiphospholipid Antibodies Standardization Group
Guido Reber
1   Haemostasis Unit, Geneva University Hospital, Switzerland
,
Inger Schousboe
2   The Panum Institute, Copenhagen, Denmark
,
Angela Tincani
3   Clinical Immunology Unit, Brescia Hospital, Italy
,
Marielle Sanmarco
4   Laboratoire d’Immunologie, Hôpital de la Conception, Marseille, France
,
Tanja Kveder
5   University Medical Center, Ljubljana, Slovenia
,
Philippe de Moerloose
1   Haemostasis Unit, Geneva University Hospital, Switzerland
,
Marie-Claire Boffa
6   Department of Internal Medicine JC Piette, Hôpital de la Pitié, Paris, France
,
Josiane Arvieux
7   Laboratoire d’Immunologie, CHU de Brest, France
› Author Affiliations
Further Information

Publication History

Received 12 February 2002

Accepted after resubmission 15 April 2002

Publication Date:
09 December 2017 (online)

Summary

Inter-laboratory variability of anti-β2-glycoprotein I antibody measurements (IgG and IgM) was investigated in the frame of the European Forum on Antiphospholipid Antibodies and its Standardization Group. Twenty-eight samples from patients with autoimmune diseases, two samples from blood donors and a set of six calibrators obtained by dilution with normal plasma of a pool of patient samples were sent to 21 European centers. Six of them used commercial kits and the others home-made assays. Marked differences in the steepness of the calibration curves obtained with the calibrator provided were observed. The standard deviations of sample measurement were high. Cut-off of positivity varied from 7 to 90 Forum Units (FU) for IgG and from 10 to 138 FU for IgM, whereas the rate of positivity varied from 50 to 93% for IgG and from 13 to 70% for IgM. No clear relationship between cut-off values and positivity rate could be established for either isotype. Adopting a common cut-off did not markedly improve the overall agreement between centers in positive/negative sample classification. Because of the majority of low positive samples, excellent concordance between centers (as defined by kappa values from 0.8 and 1) occurred only in 13% of cases for IgG and in 6% of cases for IgM, because many selected samples were low-positive. Despite the large variability of anti-β2-glycoprotein I measurements between centers, the agreement on results with highand medium-positive samples was good.

 
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