Thromb Haemost 2008; 99(01): 223-228
DOI: 10.1160/TH07-08-0515
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Thrombin generation in first-degree relatives of patients with venous thromboembolism who have factor V Leiden

A pilot study
Francis Couturaud
1   G.E.T.B.O. (Groupe d’Etude de la Thrombose de Bretagne Occidentale), EA 3878, Department of Internal Medicine and Chest Diseases
,
Jèrôme Duchemin
2   Haematology Unit, University Hospital of Brest, Brest, Francew
,
Christophe Leroyer
1   G.E.T.B.O. (Groupe d’Etude de la Thrombose de Bretagne Occidentale), EA 3878, Department of Internal Medicine and Chest Diseases
,
Bènèdicte Delahousse
3   Haematology Unit, University Hospital of Tours, Tours, France
,
Jean François Abgrall
2   Haematology Unit, University Hospital of Brest, Brest, Francew
,
Dominique Mottier
1   G.E.T.B.O. (Groupe d’Etude de la Thrombose de Bretagne Occidentale), EA 3878, Department of Internal Medicine and Chest Diseases
,
for the Groupe d’Etude de la Thrombose de Bretagne Occidentale (G.E.T.B.O)› Author Affiliations
Further Information

Correspondence to:

Dr. Francis Couturaud
GETBO, EA 3878
Department of Internal Medicine and Chest Diseases
University Hospital Centre La Cavale Blanche
29609 Brest, cedex, France
Phone: +33 2 98 34 73 48   
Fax: +33 2 98 34 79 44   

Publication History

Received: 22 August 2007

Accepted after major revision: 15 November 2007

Publication Date:
24 November 2017 (online)

 

Summary

The thrombin generation test appears to be a highly sensitive and specific test in the detection of thrombophilia in patients with venous thromboembolism. We aimed to determine the accuracy of the thrombin generation test to detect factorV Leiden and/or other prothrombotic states in first-degree relatives of patients with venous thromboembolism and factor V Leiden. Sixty-two first-degree relatives of 21 index cases were tested for factor V Leiden, the G20210A prothrombin gene mutation and thrombin generation. Information about oestrogen therapy and previousVTE was also collected. The normalized Thrombomodulin sensitivity ratio (n-TMsr) was defined as the ratio of endogenous thrombin potential determined in the presence and absence of thrombomodulin which was normalized against the same ratio determined in normal control plasma. The mean n-TMsr was 1.37 (± 0.33) in the 45 relatives with one or more prothrombotic state (factor V Leiden, G20210A prothrombin mutation, oestrogen therapy or hormonal therapy) and 1.02 (± 0.34) in the 17 relatives without prothrombotic state (p = 0.001). The positive predictive value was 90.3 (95%CI, 73.1 – 97.4). In relatives with an abnormal n-TMsr, the adjusted odds ratio for having a prothrombotic state was 8.3 (95%CI, 1.9 – 36.9) and the adjusted odds ratio for having the factor V Leiden was 14.3 (95%CI, 2.9 – 71.2).An abnormal thrombin generation test appears highly predictive for having factor V Leiden and/or other prothrombotic states in first-degree relatives of patients with venous thromboembolism and factor V Leiden.


 



Correspondence to:

Dr. Francis Couturaud
GETBO, EA 3878
Department of Internal Medicine and Chest Diseases
University Hospital Centre La Cavale Blanche
29609 Brest, cedex, France
Phone: +33 2 98 34 73 48   
Fax: +33 2 98 34 79 44