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Letter to the Editors-in-Chief| Volume 224, P1-3, April 2023

Recurrent thrombotic events after disappearance of antiphospholipid autoantibodies: A long-term longitudinal study in patients with antiphospholipid syndrome

  • Thomas Ballul
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Arthur Mageau
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Pascale Roland Nicaise
    Affiliations
    Département de Immunologie, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Nadine Ajzenberg
    Affiliations
    Laboratoire d'Hématologie, AP-HP, Hôpital Bichat-Claude Bernard, F-75018 Paris, France

    Université Paris Cité and Université Sorbonne Paris Nord, INSERM1148, LVTS, F-75018 Paris, France
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  • Andrey Strukov
    Affiliations
    Département d'Information Médicale (DIM), Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Antoine Dossier
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Diane Rouzaud
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Thomas Papo
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France
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  • Karim Sacré
    Correspondence
    Corresponding author at: Department of Internal Medicine, Bichat Hospital, APHP, 46 rue Henri Huchard, 75018 Paris, France.
    Affiliations
    Département de Médecine Interne, Hôpital Bichat, Assistance Publique Hôpitaux de Paris, Université Paris Cité, Paris, France

    Université Paris Cité, Centre de Recherche sur l'Inflammation, INSERM UMR1149, CNRS ERL8252, Faculté de Médecine site Bichat, Laboratoire d'Excellence Inflamex, Paris, France.
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Published:February 09, 2023DOI:https://doi.org/10.1016/j.thromres.2023.02.005
      Antiphospholipid syndrome (APS) is an autoimmune disease characterized by the occurrence of thrombosis and/or pregnancy morbidity related to the presence of persistent antiphospholipid autoantibodies (aPL) [
      • Miyakis S.
      • Lockshin M.D.
      • Atsumi T.
      • Branch D.W.
      • Brey R.L.
      • Cervera R.
      • et al.
      International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS).
      ]. The most frequent clinical manifestations of APS are thrombotic events and death may be caused by stroke, myocardial infarction, pulmonary embolism or catastrophic APS [
      • Cervera R.
      • Serrano R.
      • Pons-Estel G.J.
      • Ceberio-Hualde L.
      • Shoenfeld Y.
      • de Ramón E.
      • et al.
      Morbidity and mortality in the antiphospholipid syndrome during a 10-year period: a multicentre prospective study of 1000 patients.
      ]. APS treatment is based on long term anticoagulation [
      • Tektonidou M.G.
      • Andreoli L.
      • Limper M.
      • Amoura Z.
      • Cervera R.
      • Costedoat-Chalumeau N.
      • et al.
      EULAR recommendations for the management of antiphospholipid syndrome in adults.
      ].

      Keywords

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