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Antiphospholipid syndrome and systemic lupus erythematosus: Are they separate entities or just clinical presentations on the same scale?
Current Opinion in Rheumatology, 08/17/09
Shoenfeld Y et al. - A multiorgan involvement that cannot be explained by the thrombophilic state per se and similar to the well known clinical manifestations in lupus is reported in patients with primary antiphospholipid syndrome (APS). Further genetic studies, will better underline the proximity between primary APS and systemic lupus erythematosus (SLE).
Methods- APS was originally recognized only as a primary APS w/o any underlying autoimmune disease in most case
- This article addresses the issue if APS is somehow related to SLE as more than half of the APS cases later evolved into SLE
- Peculiar biological SLE markers such as an autoantibody response against chromatin antigens and complement activation have been also described in pts with primary APS
- Distinct polymorphisms of common genetic factors have been associated with SLE and primary APS supporting the notion that these entities are indeed variants within a continuum of the same disease
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