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FRI0292 Anti-phosphatidylserine/prothrombin (APS/PT) antibodies in primary antiphospholipid syndrome
  1. P Bermudez-Bermejo1,
  2. G Hernandez-Molina1,
  3. DF Hernandez-Ramirez1,
  4. V Zamora-Legoff1,
  5. E Olivares-Martínez1,
  6. AR Cabral2,
  7. CA Núñez-Alvarez1
  1. 1Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico
  2. 2Department of Medicine, The Ottawa Hospital. University of Ottawa, Ottawa, Canada

Abstract

Background Several studies have showed conflicting results regarding the presence and meaning of anti-phosphatidylserine/prothrombin (aPS/PT). However aPS/PT antibodies seem to be a risk factor for thrombosis. Nevertheless, most of the studies have focused on patients with SLE and secondary antiphospholipid syndrome (APS).

Objectives To assess the prevalence of aPS/PT antibodies, as well as their association with other antiphospholipid (aPL) antibodies (specially lupus anticoagulant [LA]) and thrombosis, in a well-established cohort of primary APS from a single center.

Methods We included 96 consecutive patients with primary APS according the Sydney classification criteria and/or patients with hematological features (thrombocytopenia and hemolytic anemia) attending a referral center in Mexico City. Patients from both groups fulfilled the Sydney laboratory criteria for APS. We registered demographics, disease duration and type of manifestation. aCL (IgG and IgM), antibodies to purified human anti-β2GP-I (IgG and IgM) and aPS/PT antibodies (IgG and IgM) were assessed by ELISA (INOVA Diagnostics). LA was determined by LA/1 screening reactant and a confirmatory test LA/2 according to published guidelines. We used chi-square (χ2) test, Spearman correlation analysis and logistic regression.

Results Most patients were females (69.7%), mean age 44.5±14.6 and median disease duration 7.3 years. The main clinical features were thrombosis (n=74, 77%), hematologic involvement (n=49 patients, 51%) and obstetric events (n=24, 25%) (non-exclusive groups). The prevalence of LA was 69.8%, aCL-IgG 56.8%, anti-β2GP-l IgG 43.1%, aCL-IgM 31.5% and anti-β2GP-I IgM 21%. The frequency of aPS/PT antibodies was 61.2% and 61.6% for IgG and IgM isotype, respectively. When we compared patients with LA+ (n=58) vs. LA- (n=25), the first group had a higher prevalence of aPS/PT-IgG (79.3% vs.16%, p=0.0001) and aPS/PT-IgM antibody (81.5% vs. 31.8%, p=0.001), as well as higher titers (aPS/PT-IgG 130.5 U vs. 8.2 U and aPS/PT-IgM 58.5 U vs. 16.6 U, p=0.0001). aPS/PT-IgG antibodies correlated with aPS/PT-IgM (ρ=0.59, p=0.0001), aCL-IgG (ρ=0.62, p=0.0001), anti-β2GP-l IgG (ρ=0.63, p=0.001) and anti-β2GP-l IgM (ρ=0.35, p=0.001). On the other hand, aPS/PT IgM antibodies correlated with aCL-IgG (ρ=0.57, p=0.0001), aCL-IgM (ρ=0.42, p=0.001), anti-β2GP-l IgG (ρ=0.48, p=0.001) and anti-β2GP-l IgM (ρ =0.59, p=0.0001). We found moderate agreement between the presence of LA and both aPS/PT isotypes (k=0.58 p=0.0001 for IgG, and k=0.47 p=0.001 for IgM). Thrombosis was associated with aPS/PT-IgG antibodies (87.7% vs. 61.1%, p=0.003) but not with aPS/PT IgM (73.6% vs. 81.8%, p=0.37). At the logistic regression analysis, the aPS/PT IgG antibodies remained associated with thrombosis after adjusting by all other aPL antibodies, OR 8.6 95% CI 2.1–33.8, p=0.002.

Conclusions In this cohort of patients with primary APS, aPS/PT antibodies were highly prevalent, correlated with other aPL antibodies and were associated independently with thrombosis.

References

  1. Sciascia S, Sanna G, Marru V, et al. Anti-prothrombin (aPT) and anti-phosphatidylserine/prothrombin (aPS/PT) antibodies and the risk of thrombosis in the antiphospholipid syndrome. Thrombosis Haemostasis 2014; 111:354–64.

References

Disclosure of Interest None declared

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