Create Account Sign In
Added value of antiphosphatidylserine/prothrombin antibodies in the workup of obstetric antiphospholipid syndrome: communication from the ISTH SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies
Author(s): ,
Katrien M.J. Devreese
Affiliations:
Department of Diagnostic Sciences, Ghent University, Ghent, Belgium
Katrien M.J. Devreese, Coagulation Laboratory, Ghent University Hospital, Corneel Heymanslaan, 10, B-9000 Ghent, Belgium.
,
Denis Wahl
Affiliations:
Université de Lorraine, Inserm, DCAC and Centre Hospitalier Regional Universitaire de Nancy, Vascular Medicine Division and Regional Competence Center for Rare Vascular and Systemic Autoimmune Diseases, Nancy, France
,
Stéphane Zuily
Affiliations:
Université de Lorraine, Inserm, DCAC and Centre Hospitalier Regional Universitaire de Nancy, Vascular Medicine Division and Regional Competence Center for Rare Vascular and Systemic Autoimmune Diseases, Nancy, France
,
Jacek Musiał
Affiliations:
Department of Internal Medicine, Jagiellonian University Medical College, Kraków, Poland
,
Gary W. Moore
Affiliations:
Department of Natural Sciences, Faculty of Science and Technology, Middlesex University, London, United Kingdom
,
Jean-Christophe Gris
Affiliations:
Department of Obstetrics and Gynecology, I.M. Sechenov First Moscow State Medical University, Moscow, Russian Federation
Arne Vandevelde
Affiliations:
Department of Diagnostic Sciences, Ghent University, Ghent, Belgium
ISTH Academy. Devreese K. 07/01/23; 409330
Katrien Devreese
Katrien Devreese
Login now to access Regular content available to all registered users.

Access to Premium content is currently a membership benefit.

Click here to join ISTH or renew your membership.

Journal Abstract
Discussion Forum (0)
Rate & Comment (0)
Background

The added value of antiphosphatidylserine/prothrombin antibodies (aPS/PT) in the diagnostic workup of antiphospholipid syndrome (APS) is unclear. Currently, diagnosis of thrombotic APS (TAPS) and obstetric APS (OAPS) requires persistent presence of lupus anticoagulant (LAC), anticardiolipin (aCL) immunoglobulin (Ig) G/IgM, or anti-β2-glycoprotein I (aβ2GPI) IgG/IgM antibodies.

Objectives

To evaluate the role of aPS/PT IgG and IgM in OAPS.

Methods

aPS/PT IgG/IgM, aCL IgG/IgM, aβ2GPI IgG/IgM, and LAC were determined in 653 patients (OAPS, TAPS, and controls). In-house aPS/PT cut-off values were calculated, titers and prevalence were compared between OAPS, TAPS, and controls and type of pregnancy morbidity. Sensitivity, specificity, likelihood ratios, and odds ratios (OR) with 95% CI were calculated.

Results

In OAPS, aPS/PT IgG and IgM showed an OR of 4.32 (95% CI, 2.54-7.36) and 3.37 (95% CI, 1.93-5.89), respectively, but the association was not independent of LAC. Prevalence and titers of aPS/PT IgG and IgM were lower in OAPS than in patients with TAPS. aPS/PT were more prevalent and showed higher titers in patients with late pregnancy loss than in patients with early pregnancy loss with a positivity of 86.4% and 39.3%, respectively. Higher aPS/PT titers did not increase the likelihood of having OAPS.

Conclusion

The added value of aPS/PT testing in the current diagnostic workup of OAPS seems limited compared with LAC, aCL, and aβ2GPI. aPS/PT might be useful in specific subsets of patients with OAPS. However, future multicentric studies are needed to elucidate the risk of less frequent and most severe obstetrical manifestations.

Abstract

Antiphosphatidylserine/prothrombin antibodies (aPS/PT) were investigated in obstetric antiphospholipid syndrome (OAPS). Prevalence and titers of aPS/PT are lower in OAPS than in thrombotic APS. aPS/PT prevalence and titers are higher in late pregnancy loss than in early pregnancy loss. Added value of aPS/PT testing in OAPS seems limited compared with current diagnostic strategies.

Code of conduct/disclaimer available in General Terms & Conditions

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies