@article{16184,
  author = {Heritier Stephane and Ioannou Y. and Zhang J. and Qi M. and Gao L. and Qi J. and Yu D. and Lau H. and Sturgess A. and Vlachoyiannopoulos P. and Moutsopoulos H. and Pericleous C. and Atsumi T. and Koike T. and Giannakopoulos B. and Krilis S. and Rahman A.},
  title = {Novel assays of thrombogenic pathogenicity in the antiphospholipid syndrome based on the detection of molecular oxidative modification of the major autoantigen beta2-glycoprotein I},
  abstract = {<p>
OBJECTIVE: Beta-2-glycoprotein I (beta2 GPI) constitutes the major autoantigen in the antiphospholipid syndrome (APS), a common acquired cause of arterial and venous thrombosis. We recently described the novel observation that beta2 GPI may exist in healthy individuals in a free thiol (biochemically reduced) form. The present study was undertaken to quantify the levels of total, reduced, and posttranslationally modified oxidized beta2 GPI in APS patients compared to various control groups. METHODS: In a retrospective multicenter analysis, the proportion of beta2 GPI with free thiols in serum from healthy volunteers was quantified. Assays for measurement of reduced as well as total circulating beta2 GPI were developed and tested in the following groups: APS (with thrombosis) (n=139), autoimmune disease with or without persistent antiphospholipid antibodies (aPL) but without APS (n=188), vascular thrombosis without APS or aPL (n=38), and healthy volunteers (n=91). RESULTS: Total beta2 GPI was significantly elevated in patients with APS (median 216.2 mug/ml [interquartile range 173.3-263.8]) as compared to healthy subjects (median 178.4 mug/ml [interquartile range 149.4-227.5] [P&lt;0.0002]) or control patients with autoimmune disease or vascular thrombosis (both P&lt;0.0001). The proportion of total beta2 GPI in an oxidized form (i.e., lacking free thiols) was significantly greater in the APS group than in each of the 3 control groups (all P&lt;0.0001). CONCLUSION: This large retrospective multicenter study shows that posttranslational modification of beta2 GPI via thiol-exchange reactions is a highly specific phenomenon in the setting of APS thrombosis. Quantification of posttranslational modifications of beta2 GPI in conjunction with standard laboratory tests for APS may offer the potential to more accurately predict the risk of occurrence of a thrombotic event in the setting of APS.
</p>
},
  year = {2011},
  journal = {Arthritis and Rheumatism},
  volume = {63},
  edition = {2011/05/28},
  number = {9},
  pages = {2774-82},
  isbn = {1529-0131 (Electronic)0004-3591 (Linking)},
  note = {Ioannou, YiannisZhang, Jing-YunQi, MiaoGao, LuQi, Jian ChengYu, De-MinLau, HermanSturgess, Allan DVlachoyiannopoulos, Panayiotis GMoutsopoulos, Haralampos MRahman, AnisurPericleous, CharisAtsumi, TatsuyaKoike, TakaoHeritier, StephaneGiannakopoulos, BillKrilis, Steven A17821/Arthritis Research UK/United Kingdom18491/Arthritis Research UK/United KingdomMulticenter StudyResearch Support, Non-U.S. Gov'tUnited StatesArthritis Rheum. 2011 Sep;63(9):2774-82. doi: 10.1002/art.30383.},
  language = {eng},
}