Prekallikrein (PK), also known as Fletcher factor, is a 85,000 Mr serine protease that complexes with HK. PK is the precursor of plasma kallikrein, which is a serine protease that activates kinins. PK is cleaved to produce kallikrein by Factor XII (Hageman factor). [1]
Prekallikrein Deficiency
Hereditary deficiencies in PK are very rare. They can cause a prolonged APTT, which can be corrected by incubation of the patient’s plasma.
Deficiencies in PK can also be acquired due to some disease states, such as angioedema, infection, DIC, and sickle-cell disease.[1]
Although most cases of prekallikrein deficiency are asymptomatic, a few reports link severe prekallikrein deficiency with thrombotic phenomena and recurrent pregnancy loss. More recently, a case of prekallikrein deficiency was shown to be associated with severe mucosal bleeding.[2]
Discovery of Prekallikrein
PK was initially described by Hathaway et al. in 1965 after encountering a Kentucky family who exhibited strikingly abnormal APTT results, but showed no bleeding symptoms. The family appeared to have a hereditary deficiency in an unknown coagulation factor, dubbed “Fletcher factor” after the family. In 1973 Kirk Wuepper determined that Fletcher factor and prekallikrein were the same.[3]
References
- ^ a b Goodnight, SH Jr, Hathaway, WE. "Disorders of Hemostasis and Thrombosis." Second edition. 2001.
- ^ Dasanu CA, et al. "A Case of Prekallikrein Deficiency Resulting in Severe Recurrent Mucosal Hemorrhage". American Journal of Medical Sciences, 2009.
- ^ OMIM article on prekallikrein deficiency
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