Key result
Heparin interaction with platelet factor 4 (PF4) triggers an immune-mediated, prothrombotic response causing heparin-induced thrombocytopenia (HIT), more commonly with UFH than LMWH.
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Heparin, a negatively charged glycosaminoglycan (3,000-30,000 Da), is an anticoagulant released by mast cells and basophils during the normal clotting process [ 1 ]. Heparin is widely used for the treatment and prophylaxis of thromboembolic diseases in medical and surgical patients [ 1 ]. Heparin-induced thrombocytopenia (HIT) is one of the most serious adverse events associated with this drug. HIT is an immune-mediated, prothrombotic complication that occurs with unfractionated heparin (UFH) and to a lesser extent with low-molecular-weight heparin (LMWH) [ 2 ]. The fundamental paradox of HIT results from a platelet-activating immune response triggered by the interaction of heparin with a specific platelet protein, platelet factor 4 (PF4) [ 3 ].
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Yasser Sakr (2011) conducted a review in Heparin-induced thrombocytopenia (HIT). Heparin (unfractionated heparin and low-molecular-weight heparin) was evaluated. Heparin interaction with platelet factor 4 (PF4) triggers an immune-mediated, prothrombotic response causing heparin-induced thrombocytopenia (HIT), more commonly with UFH than LMWH.
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