Thromb Haemost 1997; 77(03): 472-476
DOI: 10.1055/s-0038-1655991
Clinical Studies
Schattauer GmbH Stuttgart

Increased Tissue Factor Pathway Inhibitor (TFPI) and Coagulation in Patients with Insulin-dependent Diabetes mellitus

Authors

  • Paul B Leurs

    The Department of Internal Medicine, Division of Endocrinology and Metabolism, and Division of Hematology, University Hospital, Maastricht, The Netherlands
  • Rene van Oerle

    The Department of Internal Medicine, Division of Endocrinology and Metabolism, and Division of Hematology, University Hospital, Maastricht, The Netherlands
  • Bruce H R Wolffenbuttel

    The Department of Internal Medicine, Division of Endocrinology and Metabolism, and Division of Hematology, University Hospital, Maastricht, The Netherlands
  • Karly Hamulyak

    The Department of Internal Medicine, Division of Endocrinology and Metabolism, and Division of Hematology, University Hospital, Maastricht, The Netherlands
Further Information

Publication History

Received 10 June 1996

Accepted after revision 30 October 1996

Publication Date:
11 July 2018 (online)

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Summary

Recently, we found an increase in tissue factor pathway inhibitor (TFPI) activity in patients with insulin-dependent diabetes mellitus (IDDM). This increase in TFPI activity could be the result of increased thrombin formation and/or altered binding of TFPI to glycosaminoglycans. We studied TFPI activity (chromogenic assay) in relation to prothrombin F1+2 fragments and endogenous thrombin potential (ETP), in 46 IDDM patients, and 18 age and sex-matched healthy controls. Prothrombin, antithrombin and thrombomodulin were also determined. In IDDM patients, TFPI activity and F1+2 levels were significantly higher, while ETP, prothrombin antigen levels, and antithrombin activity were lower as compared to the controls. In IDDM patients with microalbuminuria, a manifestation of generalized angiopathy, TFPI activity, F1+2 and thrombomodulin levels were higher than in patients with only retinopathy or patients without complications. No correlation between TFPI activity, F1+2 levels and thrombomodulin was found, while TFPI activity was negatively correlated with ETP (r = -0.27). Microalbuminuria was significantly correlated with TFPI activity (r = 0.46), F1+2 (r = 0.56), and thrombomodulin (r = 0.52). In TFPI-depleted plasma, ETP increased, indicating that ETP is affected by TFPI. In conclusion, the increase in TFPI activity in IDDM patients may not be considered to be a reaction on a procoagulant state. It is hypothesized that vascular damage, leading to alterations in glycosaminoglycans, is in part responsible for the changes in TFPI activity, F1+2 levels and ETP.