Anticardiolipin Syndrome
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Definition of Anticardiolipin Syndrome
The antiphospholipid (anticardiolipin) syndrome (APS) is characterized by recurrent venous or arterial thrombosis (clots), recurrent fetal loss, and thrombocytopenia (a reduction in the number of platelets). Antiphospholipid antibody syndrome can be either primary or secondary to other diseases such as lupus.
Description of Anticardiolipin Syndrome
Antiphospholipid antibody (aPL) is an antibody that reacts with negatively charged phospholipids, molecules which are common constituents of cell membranes. Two primary aPLs are lupus anticoagulant and anticardiolipin antibody. Although the term 'anticoagulant' would imply a tendency for bleeding (anti (against) + coagulant (clotting)), in fact, these antibodies tend to increase clot formation. Such antibodies are often found in association with pathological conditions, including thrombosis (clotting), fetal loss, and thrombocytopenia (low platelets). However, such antibodies are also found in some individuals with no apparent ill effects, so that the role of these antibodies remains unclear.
The primary consequence of the antiphospholipid antibody is non-inflammatory thromboembolic (clotting) disease. Virtually all venous and arterial systems have been cited, including large, medium, and small vessels.
The most common site for venous thrombosis is in the leg, in the femoral and popliteal (the posterior region of the knee) systems, whereas cerebral ischemia (low blood blow to the brain), manifested as embolic strokes and transient ischemic attacks (TIAs), is the most commonly reported arterial presentation.
Anticardiolipin Antibodies and Pregnancy.
Pregnant patients who have anticardiolipin antibodies are at increased risk for miscarriage, fetal growth retardation and stillbirth.
Anticardiolipin Antibodies and Heart Attacks (Myocardial Infarction).
The presence of lupus anticoagulants and anticardiolipin antibodies (aCL) has been associated with young victims of myocardial infarction (heart attack).
