Antiphospholipid Syndrome
- PMID: 28613698
- Bookshelf ID: NBK430980
Antiphospholipid Syndrome
Excerpt
Antiphospholipid antibodies (APLAs) are autoantibodies that target phospholipid-binding proteins. Antiphospholipid syndrome (APS) is a multisystemic autoimmune disorder. The hallmark of APS comprises the persistent presence of APLAs in the setting of arterial and venous thrombus or pregnancy loss.
The most common sites for venous and arterial thrombosis are the lower limbs and cerebral arterial circulation, respectively. However, thrombosis can occur in any organ. Laboratory tests, including enzyme-linked immunosorbent assay (ELISA) and functional assays, are used to identify APS. The 3 known APLAs include:
Anticardiolipin antibodies IgG or IgM (ELISA)
Anti-beta-2-glycoprotein-I (anti-β2GPI) antibodies IgG or IgM (ELISA)
Lupus anticoagulants (functional clotting assays)
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Sections
- Continuing Education Activity
- Introduction
- Etiology
- Epidemiology
- Pathophysiology
- Histopathology
- History and Physical
- Evaluation
- Treatment / Management
- Differential Diagnosis
- Prognosis
- Complications
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References
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- Knight JS, Branch DW, Ortel TL. Antiphospholipid syndrome: advances in diagnosis, pathogenesis, and management. BMJ. 2023 Feb 27;380:e069717. - PubMed
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- Garcia D, Erkan D. Diagnosis and Management of the Antiphospholipid Syndrome. N Engl J Med. 2018 Sep 27;379(13):1290. - PubMed
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- Levine JS, Branch DW, Rauch J. The antiphospholipid syndrome. N Engl J Med. 2002 Mar 07;346(10):752-63. - PubMed
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- Arvieux J, Renaudineau Y, Mane I, Perraut R, Krilis SA, Youinou P. Distinguishing features of anti-beta2 glycoprotein I antibodies between patients with leprosy and the antiphospholipid syndrome. Thromb Haemost. 2002 Apr;87(4):599-605. - PubMed
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