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ProC Global: the first functional screening assay for the complete protein C pathway.
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Citations
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References
1997
Year
ImmunologyMolecular BiologyPathologyLeiden MutationProteomic TechnologyThrombosisVenous ThrombosisProtein ExpressionProtein C PathwayHematologyProc GlobalClinical ChemistryBleeding DisorderLaboratory MedicineMolecular DiagnosticsAtherosclerosisProteomicsCell SignalingProtein FunctionProtein CVascular BiologyPathway AnalysisGene ExpressionCell BiologyThrombopoiesisNatural SciencesHemostasisCoagulopathyCellular BiochemistryMedicine
In clinical practice, venous thromboembolic complications are much more frequent than bleeding disorders. In fact, disturbances within the protein C pathway due to coagulation factor V (FV) Leiden mutation and deficiency of protein C or protein S are the most frequent abnormalities in hereditary thrombophilia. Furthermore, acquired dysfunctions of the protein C system may predispose the single individual to an increased thrombotic risk. A routine-suited screening assay that would allow the monitoring of the proper interplay of factors in the protein C pathway could add an important factor to the basic coagulation profile. This consists of the prothrombin time and of the activated partial thromboplastin time, which currently allow only a screening for increased risk for bleeding but not for venous thromboembolism. A new functional screening test for the protein C system such as the presented ProC Global should therefore facilitate detection of FV Leiden as well as deficiency of protein C and protein S. The results of the present evaluation indicate that ProC Global is highly sensitive to activated protein C resistance/FV Leiden (100%) and protein C deficiency (90%) and sensitive to protein S deficiency (63%). Furthermore, the assay gives a quantitative measure of the net potential of the protein C pathway in relation to the intrinsic procoagulant system. The use of this assay for a prospective assessment of thromboembolic risk is the subject of current studies.
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