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Antiphospholipid antibodies and the brain: a consensus report
R L Brey1, E Muscal, J Chapman
1University of Texas Health Science Center at San Antonio, Department of Neurology, San Antonio, TX 78229, USA. brey@uthscsa.edu
Antiphospholipid antibodies (aPL) are linked to ischemic stroke risk, especially recurrent events. Systemic lupus erythematosus (SLE) may heighten this risk, alongside other neurological issues like cognitive dysfunction and seizures.
Area of Science:
- Neurology
- Immunology
- Rheumatology
Background:
- Antiphospholipid antibodies (aPL) are associated with an increased risk of thrombotic events, including ischemic stroke.
- The role of aPL in predicting first versus recurrent ischemic stroke requires further clarification.
- The interplay between aPL, systemic lupus erythematosus (SLE), and neurological manifestations is not fully understood.
Purpose of the Study:
- To differentiate the predictive value of aPL for first-time versus recurrent ischemic stroke.
- To investigate whether concurrent SLE exacerbates aPL-related stroke risk.
- To explore the association between aPL and common neurological conditions such as cognitive dysfunction, headache, multiple sclerosis, and seizures/epilepsy.
Main Methods:
- This report synthesizes existing literature and clinical data.
- It analyzes studies examining aPL prevalence and neurological outcomes.
- The review focuses on identifying patterns and risk associations.
Main Results:
- aPL are significant predictors of both first and recurrent ischemic stroke.
- Concomitant SLE appears to amplify the stroke risk associated with aPL.
- Associations were observed between aPL and cognitive dysfunction, headache, multiple sclerosis, and seizures/epilepsy.
Conclusions:
- aPL represent a critical risk factor for ischemic stroke, particularly recurrent events.
- SLE presence increases the thrombotic risk in aPL-positive individuals.
- Further research is essential to fully elucidate the mechanisms and management strategies for aPL-associated neurological disorders.
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