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Beta-2-glycoprotein I antibodies in patients with thrombosis

The laboratory diagnosis of antiphospholipid antibody syndrome currently requires two consecutive positive results in either lupus anticoagulant or anticardiolipin antibody assays. Antibodies against beta-2-glycoprotein I (a 2-GPI) are suggested as a new marker for the syndrome. The inclusion of a 2...

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Bibliographic Details
Published in:Scandinavian journal of clinical and laboratory investigation 2003, Vol.63 (2), p.111-118
Main Authors: EBELING, F., PETTERSSON, T., MUUKKONEN, L., VAHTERA, E., RASI, V.
Format: Article
Language:English
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Summary:The laboratory diagnosis of antiphospholipid antibody syndrome currently requires two consecutive positive results in either lupus anticoagulant or anticardiolipin antibody assays. Antibodies against beta-2-glycoprotein I (a 2-GPI) are suggested as a new marker for the syndrome. The inclusion of a 2-GPI in the official diagnostic criteria has so far been precluded owing to lack of an international standard and also technical difficulties. Samples from 5367 consecutive patients sent to a national reference laboratory mainly because of various thrombotic events were studied. An IgG a 2-GPI ELISA assay was performed in addition to lupus anticoagulant (dRVVT and PTT-LA) and IgG anticardiolipin antibody determinations to evaluate patient groups in which the new assay might be of value. From a total of 90 patients, 2.2% of the samples were a 2-GPI positive; 51 patients had a 2-GPI as the only positive antiphospholipid antibody marker; 20 patients had had a venous thrombosis and 14 an arterial thrombosis, 4 had pregnancy complications and 2 had thrombocytopenia. Relatively young patients with cerebrovascular ischaemic events seemed especially to present sole a 2-GPI positivity. The a 2-GPI positivity remained fairly constant in the 23 patients from whom follow-up samples were taken. It is concluded that the IgG a 2-GPI assay seems to be a potentially important additional diagnostic tool for the antiphospholipid antibody syndrome.
ISSN:0036-5513
1502-7686
DOI:10.1080/00365510310002086