Anti-prothrombin (aPT) and anti-phosphatidylserine/prothrombin (aPS/PT) antibodies and the risk of thrombosis in the antiphospholipid syndrome

作者：Sciascia Savino; Sanna Giovanni; Murru Veronica; Roccatello Dario; Khamashta Munther A; Bertolaccini Maria Laura^*

来源：Thrombosis and Haemostasis, 2014, 111(2): 354-364.

DOI：10.1160/TH13-06-0509

• Antiphospholipid antibodies
• antiphospholipid syndrome
• venous thrombosis
• stroke

Antibodies to prothrombin are detected by directly coating prothrombin on irradiated ELISA plates (aPT) or by using the phosphatidylserine/prothrombin complex as antigen (aPS/PT). Although these anti bodies have both been associated with antiphospholipid syndrome; (APS) and a correlation between the two assays have been reported, it seems that aPT and aPS/PT belong to different populations of autoantibodies. It was our objective to systematically review the available 1 evidence on aPT and aPS/PT antibodies and the risk of thrombosis in APS. Medline-reports published between 1988 and 2013 investigating aPT and aPS/PT as a risk factor for thrombosis were included. When, ever possible, antibody isotype(s) and site of thrombosis were analysed. This systematic review is based on available data from more; than 7,000 patients and controls from 38 studies analysing aPT and 10 aPS/PT. Antibodies to prothrombin (both a PT and aPS/PT) increased the risk of thrombosis (odds ratio [OR] 2.3; 95% confidence interval [Cl] 1.72-3.5). aPS/PT seemed to represent a stronger risk factor for thrombosis, both arterial and/or venous than aPT (OR 5.11; 95%CI 4.2-6.3 and OR 1.82; 95%CI 1.44-2.75, respectively). In conclusion, routine measurement of aPS/PT (but not aPT) might be useful in establishing the thrombotic risk of patients with previous thrombosis and/or systemic lupus erythematosus. Their inclusion as laboratory criteria for the APS should be indisputably further explored.

• 出版日期2014-2