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Prepublished online as a Blood First Edition Paper on October 3, 2002; DOI 10.1182/blood-2002-02-0441.
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Blood, 1 March 2003, Vol. 101, No. 5, pp. 1827-1832
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
Lupus anticoagulants are stronger risk factors for
thrombosis than anticardiolipin antibodies in the antiphospholipid
syndrome: a systematic review of the literature
Monica Galli,
Davide Luciani,
Guido Bertolini, and
Tiziano Barbui
From the Division of Hematology, Ospedali Riuniti,
Bergamo, Italy; and Laboratory of Clinical Epidemiology,
Mario Negri Institute, Ranica (Bergamo), Italy.
To formally establish the risk of lupus anticoagulants and
anticardiolipin antibodies for arterial and venous thrombosis, we ran a
MEDLINE search of the literature from 1988 to 2000. Studies were
selected for their case-control (11), prospective (9), cross-sectional (3), and ambispective (2) design. They provided or enabled us to
calculate the odds ratio with 95% confidence interval (CI) of lupus
anticoagulants and/or anticardiolipin antibodies for thrombosis in 4184 patients and 3151 controls. Studies were grouped according to the
antibody investigated. Five studies compared lupus anticoagulants with
anticardiolipin antibodies: the odds ratio with 95% CI of lupus
anticoagulants for thrombosis was always significant. None of them
found anticardiolipin antibodies were associated with thrombosis. Four
studies analyzed only lupus anticoagulants: the odds ratio with 95% CI
was always significant. The risk of lupus anticoagulants was
independent of the site and type of thrombosis, the presence of
systemic lupus erythematosus, and the coagulation tests employed to
detect them. Sixteen studies served to assess 28 associations between
anticardiolipin antibodies and thrombosis: the odds ratio with 95% CI
was significant in 15 cases. Anticardiolipin titer correlated with the
odds ratio of thrombosis. In conclusion, the detection of lupus
anticoagulants and, possibly, of immunoglobulin G (IgG) anticardiolipin
antibodies at medium or high titers helps to identify patients at risk
for thrombosis. However, to take full advantage of the conclusions
provided by the available evidence, there is an urgent need to
harmonize investigational methods.

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