Literature DB >> 19085768

Standardization and clinical utility of thrombin-generation assays.

Erik Berntorp1, Gian Luca Salvagno.   

Abstract

Thrombin generation is a key process that determines the extent of a hemostatic plug or a thrombotic process. The ensuing thrombin burst is crucial for the formation of a stable fibrin clot. During its active life, thrombin exerts a multitude of highly regulated actions on the blood and the vessel wall, including the clotting of fibrinogen. The inappropriate generation of thrombin may lead to pathologic processes, foremost of which are hemorrhagic or thrombotic diseases. The coagulation system is usually investigated by means of two in vitro classic clotting tests, the activated partial thromboplastin time (APTT) and prothrombin time (PT), which assess only time to initiation of clot formation and do not entirely reflect global hemostatic balance. The APTT and PT permit identification of connectivity between the component activities identified as required for plasma coagulation and define the concept of intrinsic and extrinsic coagulation pathways, which converge at the point of formation of the prothrombinase complex. However, the mechanisms established by in vitro tests are not always mirrored in the human pathologies associated with bleeding or thrombosis. The recent development of newer tests based on the continuous registration of thrombin generation under in vitro conditions that mimic more closely what occurs in vivo prompt a reinvestigation of the balance between procoagulants and anticoagulants in patients with various hemostatic disorders. Thrombin-generation assays not only provide an overall assessment of hemostasis but also target potential extrahemostatic effects of the generated thrombin, a potent agonist of a multitude of cellular activation pathways. Moreover, estimation of an individual's thrombin-generation potential may correlate more closely with a hypercoagulable or hypocoagulable phenotype when compared with traditional coagulation tests. In this review, we discuss to what extent thrombin generation can be expected to reflect the clotting function of blood, the development and use of different thrombin-generation assay systems suitable for detecting changes in the kinetics of thrombin generation, and the clinical utility of thrombin generation.

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Year:  2008        PMID: 19085768     DOI: 10.1055/s-0028-1104546

Source DB:  PubMed          Journal:  Semin Thromb Hemost        ISSN: 0094-6176            Impact factor:   4.180


  17 in total

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Review 4.  Coagulopathy in liver disease: Lack of an assessment tool.

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5.  Tailored glycopolymers as anticoagulant heparin mimetics.

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Journal:  Angew Chem Int Ed Engl       Date:  2013-10-09       Impact factor: 15.336

6.  Factor Xa generation by computational modeling: an additional discriminator to thrombin generation evaluation.

Authors:  Kathleen E Brummel-Ziedins; Thomas Orfeo; Matthew Gissel; Kenneth G Mann; Frits R Rosendaal
Journal:  PLoS One       Date:  2012-01-11       Impact factor: 3.240

7.  Thrombin generation assays for global evaluation of the hemostatic system: perspectives and limitations.

Authors:  Rita Carolina Figueiredo Duarte; Cláudia Natália Ferreira; Danyelle Romana Alves Rios; Helton José Dos Reis; Maria das Graças Carvalho
Journal:  Rev Bras Hematol Hemoter       Date:  2017-05-09

8.  The prothrombotic phenotypes in familial protein C deficiency are differentiated by computational modeling of thrombin generation.

Authors:  Kathleen E Brummel-Ziedins; Thomas Orfeo; Peter W Callas; Matthew Gissel; Kenneth G Mann; Edwin G Bovill
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

9.  Thrombin generation as marker to estimate thrombosis risk in patients with abnormal test results in lupus anticoagulant routine diagnostics.

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Journal:  Thromb J       Date:  2013-11-12

10.  Thrombin Generating Capacity and Phenotypic Association in ABO Blood Groups.

Authors:  Romy M W Kremers; Abdulrahman B O Mohamed; Leonie Pelkmans; Salwa Hindawi; H Coenraad Hemker; H Bas de Laat; Dana Huskens; Raed Al Dieri
Journal:  PLoS One       Date:  2015-10-28       Impact factor: 3.240

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