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Abstract Number: 2866

External Validation of the Global Anti-Phospholipid Syndrome Score in Comparison to IgG Antibodies Directed Against Domain I of ß2-Glycoprotein I. a Prospective Multicentre Cohort Study

Stephane Zuily1, Bas De Laat2, Veronique Regnault3, Pierre Kaminsky4, Hilde Kelchtermans5, Zakera Shums6, Roger Albesa7, Gary L Norman6, Philip de Groot8, Anne-Christine Rat9, Jacques Ninet10, Nadine Magy-Bertrand11, Jean-Louis Pasquali12, Marc Lambert13, Bernard Lorcerie14, Thomas Lecompte15, Francis Guillemin16 and Denis Wahl17, 1CHU de Nancy, Vascular Medicine Division and Regional Competence Center For Rare Vascular And Systemic Autoimmune Diseases, Nancy, F-54000, France; Inserm, UMR_S 1116, Nancy, F-54000, France; Université de Lorraine, Nancy, F-54000, France, Nancy, France, 2Biochemistry, CARIM, Maastricht University, Maastricht, Netherlands, 3Inserm, UMR_S 1116, Nancy, F-54000, France; Université de Lorraine, Nancy, F-54000, France; CHU de Nancy, Contrat d’interface, Nancy, F-54000, France, Nancy, France, 4Internal Medicine, CHU Nancy, Vandoeuvre, France, 5Biochemistry, CARIM, Maastricht University, The Netherlands; Synapse BV, Maastricht, The Netherlands, Maastricht, Netherlands, 6INOVA Diagnostics, San Diego, CA, 7Research, INOVA Diagnostics, San Diego, CA, 8Clinical Chemistry and Hematology, UMC Utrecht, The Netherlands, Utrecht, Netherlands, 9University Paris Descartes, EA 4360 APEMAC, University of Lorraine, Nancy, France, 10Department of Nephrology and Internal Medicine, Hôpital Edouard Herriot, Lyon, France, Lyon, France, 11Bensançon University Hospital, Besançon, France, 12Service de Medecine Interne, Nouvel Hospital Civil, Strasbourg Cedex, France, 13Lille University Hospital, Lille, France, 14Hopital Du Bocage, Service de Médecine Interne et Immunologie Clinique, Dijon, France, 15Inserm, UMR_S 1116, Nancy, F-54000, France; Université de Lorraine, Nancy, F-54000, France; CHU de Nancy, Haematology Laboratory, Nancy, F-54000, France; Division of Haematology, HUG, Geneva, Switzerland (current address), Geneva, Switzerland, 16INSERM, Centre d'Investigation Clinique - Epidémiologie Clinique (CIC-EC) CIE6, Nancy, France, 17Regional Competence Center For Rare Vascular And Systemic Autoimmune Diseases, Nancy University Hospital and INSERM U961, Vandoeuvre-Les-Nancy, France

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Antiphospholipid antibodies, antiphospholipid syndrome, systemic lupus erythematosus (SLE) and thrombosis

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Session Information

Title: Antiphospholipid Syndrome

Session Type: Abstract Submissions (ACR)

Background/Purpose: Our objectives were 1- to perform an external validation of the Global Anti-Phospholipid Syndrome Score (GAPSS) and 2- to compare prognostic significances of GAPPS and a novel assays IgG antibodies directed against domain I of ß2-glycoprotein I (antiDI) in patients with antiphospholipid antibodies (aPL) and/or systemic lupus erythematosus (SLE).

Methods: We performed a prospective cohort study in French University Hospitals. Consecutive patients with aPL and/or SLE according to ACR classification without ongoing anticoagulant treatment were enrolled. The outcome was the time to the first incident thrombotic event. Blood was drawn at baseline. ELISA antiDI and anti-phosphatidyl/prothrombin antibodies assays were performed together with traditional assays (lupus anticoagulant, anticardiolipin and anti-ß2-glycoprotein I antibodies). GAPSS was computed for each patient.

Results: One hundred and thirty eight patients (median age 43.5±15.3 years; 108 women) were followed-up for a mean duration of 43±20.7 months (493.9 patient-years). Thrombosis during follow-up occurred in 16 patients (3 strokes, 1 myocardial infarction, 1 splanchnic arterial thrombosis, 3 pulmonary embolisms, 3 deep vein, 5 small vessels thromboses). Higher values of GAPSS were seen in patients who experienced thrombosis compared to those without (10.9±4.8 vs 7.9±5.4, p=0.03). While triple positivity (HR=2.38 [CI95%; 0.83-6.80], p=0.11) and GAPSS above 10 (HR=1.56 [CI95%; 0.55-4.47], p=0.41) were not predictive of further incident thrombotic events, GAPSS above 16 (HR=5.27 [CI95%; 1.16-23.93], p=0.03) and high levels of antiDI above the 90th percentile of patients (HR=5.64 [CI95%; 1.94-16.42], p=0.002) were highly predictive of incident thrombotic events.

Conclusion: GAPSS and high levels of antiDI are significant predictors of thrombosis in aPL/SLE patients. These antibodies seem to add a substantial improvement in risk prediction of thrombosis independently of clinical variables assessed by GAPSS’ components.


Disclosure:

S. Zuily,
None;

B. De Laat,
None;

V. Regnault,
None;

P. Kaminsky,

SHIRE HGT,

6,

Genzyme Corporation,

6;

H. Kelchtermans,
None;

Z. Shums,

Inova Diagnostics, Inc.,

3;

R. Albesa,

Inova Diagnostics, Inc.,

3;

G. L. Norman,

Inova Diagnostics, Inc.,

3;

P. de Groot,
None;

A. C. Rat,
None;

J. Ninet,
None;

N. Magy-Bertrand,
None;

J. L. Pasquali,
None;

M. Lambert,
None;

B. Lorcerie,
None;

T. Lecompte,
None;

F. Guillemin,
None;

D. Wahl,
None.

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