Rheumatology Advance Access published online on May 31, 2005
Rheumatology, doi:10.1093/rheumatology/keh698
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1 Department of Neurology, Division of Angiology, University Hospital, JW Goethe University Frankfurt, Germany
* To whom correspondence should be addressed. Objective. Antiphospholipid antibodies (APLA) are established risk factors for venous thrombosis but their role in the pathogenesis of cerebral ischaemia is unclear. The purpose of the present study was to evaluate the relevance of various APLA in patients with cryptogenic stroke (group A, n = 21) and determined causes of stroke (group B, n = 104) according to the TOAST classification in comparison with healthy volunteers without any thrombotic or ischaemic event in their history (group C, n = 84). Methods. Median ages were 52 yr (A), 60 yr (B) and 51 yr (C). Blood samples were tested for lupus anticoagulant (LA) using phospholipid-dependent coagulation tests (activated partial thromboplastin time, diluted Russell viper venom time). Confirmatory tests were performed if necessary. Furthermore, we assessed the presence of specific APLA and their antibody subclasses against cardiolipin (AclA), phosphatidylserine (ApsA), phosphatidylinositol (ApiA) and beta-2-glycoprotein I (A Results. For ApsA IgG we found a significantly higher prevalence in stroke patients (57.7%) compared with normal subjects (4.8%; P<0.001). Similarly, A Conclusion. The results of this study suggest a relevant role for antiphosphatidylserine IgG and anti-
Received December 29, 2004
Accepted April 29, 2005
Original Papers
Phosphatidylserine IgG and beta-2-glycoprotein I IgA antibodies may be a risk factor for ischaemic stroke
2 Department of Neurology, Division of Angiology, University Hospital, JW Goethe University Frankfurt, Germany; Department of Internal Medicine, Division of Angiology, University Hospital, JW Goethe University Frankfurt, Germany
3 Department of Internal Medicine, Division of Angiology, University Hospital, JW Goethe University Frankfurt, Germany
T. Kahles, E-mail: t.kahles{at}em.uni-frankfurt.de
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Abstract
2A) using enzyme-linked immunosorbent assay.
2A IgA was significantly more prevalent in stroke patients (20.8%) in comparison with normals (3.6%; P<0.001). For all other APLAs tested, no significant differences emerged after adjustment for multiple comparisons. We did not find significant differences between stroke subtypes for any APLA.
2-glycoprotein I IgA in stroke aetiology.
2-GP I; Antiphosphatidylserine.
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