Testing for
antiphospholipid antibodies could be an important part in determining the cause of a cerebrovascular event (CVE). Currently, it is also unknown whether
antiphospholipid antibodies represent a risk factor for the development of a CVE and whether the selected
therapy options are efficacious. So, this study aimed at (1) determining the frequency of patients experiencing a CVE and fulfilling the laboratory criterion for an
antiphospholipid syndrome (APS), (2) investigating whether the persistent presence of
antiphospholipid antibodies represented a risk factor for a CVE, and (3) focusing on the efficacy of the selected treatment strategy in the first year after the CVE. Eighty-nine patients with an acute CVE were prospectively followed for 1 year. At least two sera from each were tested for lupus
anticoagulants, anticardiolipin, anti-β2-glycoprotein I, anti-
phosphatidylserine/
prothrombin and anti-
annexin V antibodies. Twenty out of eighty-nine (22%) of CVE patients fulfilled the criteria for APS (17/20 for definitive and 3 for probable APS). There was a significant association between persistently present
antiphospholipid antibodies and the CVE (OR, 4.62). No statistically significant difference was found in the CVE recurrence rate between APS-CVE and non-APS-CVE patients being treated mainly with acetyl
salicylic acid.
Antiphospholipid antibodies represent an independent risk factor for a CVE. In the first year after the CVE, antiplatelet
therapy seemed to be sufficient in secondary CVE thromboprophylaxis in most APS patients.