Thromb Haemost 1984; 51(01): 001-005
DOI: 10.1055/s-0038-1660995
Original Article
Schattauer GmbH Stuttgart

The Use of a Functional and Immunologic Assay for Plasma Protein C in the Study of the Heterogeneity of Congenital Protein C Deficiency

Authors

  • R M Bertina

    The Haemostasis and Thrombosis Research Unit, Department of internal Medicine, Leiden University Hospital, Leiden, The Netherlands
  • A W Broekmans

    The Haemostasis and Thrombosis Research Unit, Department of internal Medicine, Leiden University Hospital, Leiden, The Netherlands
  • C Krommenhoek-van Es

    The Haemostasis and Thrombosis Research Unit, Department of internal Medicine, Leiden University Hospital, Leiden, The Netherlands
  • A van Wijngaarden

    The Haemostasis and Thrombosis Research Unit, Department of internal Medicine, Leiden University Hospital, Leiden, The Netherlands
Further Information

Publication History

Received 30 August 1983

Accepted 12 October 1983

Publication Date:
19 July 2018 (online)

Preview

Summary

Protein C is a vitamin K dependent protein involved in blood coagulation. A congenital deficiency in protein C antigen - which inherits as an autosomal dominant disorder - has been reported to be associated with a high risk for thrombo-embolic disease at relatively young age. In the present paper we report on the development of a functional assay for plasma protein C. In this assay protein C is adsorbed to Al(OH)3, eluted and activated by thrombin, after which the concentration of the activated protein C is measured with a peptide substrate (S2366). Normal values for protein C activity and protein C antigen were determined in healthy volunteers and patients on stable oral anticoagulant treatment. Protein C activity and antigen levels were compared in 28 patients from 9 different pedigrees with both congenital protein C deficiency and thrombotic disease. Two types of protein C deficiency could be recognized: in type I the deficiency is due to the absence or reduced presence of protein C molecules, while in type II the deficiency is caused by the presence of an abnormal protein C molecule with strongly reduced functional activity.