Download PDF
Thromb Haemost 2013; 109(03): 361-362
DOI: 10.1160/TH13-01-0039
Invited Editorial Focus
Schattauer GmbH

Family history of VTE: An easy tool to score the individual risk

Maurizio Margaglione
1   Medical Genetics, Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy
› Author Affiliations
Further Information

Publication History

Received: 15 January 2013

Accepted: 15 January 2013

Publication Date:
29 November 2017 (online)

    Permissions and Reprints

Editorial Focus on: Zöller et al. Thromb Haemost2013; 109: 458-463.

Refers to:

Familial risk of venous thromboembolism in first-, second- and third-degree relatives: a nationwide family study in SwedenThromb Haemost 2013; 109(03): 458-463
DOI: 10.1160/TH12-10-0743

 

  • References

  • 1 White RH. The epidemiology of venous thromboembolism. Circulation 2003; 107 (Suppl. 01) I4-8.
    PubMedGoogle Scholar
  • 2 Bezemer ID, van der Meer FJM, Eikenboom JC. et al. The value of family history as a risk indicator for venous thrombosis. Arch Intern Med 2009; 169: 610-615.
    CrossrefPubMedGoogle Scholar
  • 3 Margaglione M, Grandone E. Population genetics of venous thromboembolism. A narrative review. Thromb Haemost 2011; 105: 221-231.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 4 Larsen TB, Sorensen HT, Skytthe A. et al. Major genetic susceptibility for venous thromboembolism in men: a study of Danish twins. Epidemiology 2003; 14: 328-332.
    PubMedGoogle Scholar
  • 5 Rojnuckarin P, Uaprasert N, Vajragupta L. et al. Risk factors for symptomatic venous thromboembolism in Thai hospitalised medical patients. Thromb Haemost 2011; 106: 1103-1108.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 6 Zöller B, Ohlsson H, Sundquist J. et al. Familial risk of venous thromboembolism in first-, second- and third-degree relatives: a nationwide family study in Sweden. Thromb Haemost 2013; 109: 458-463.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 7 Zoller B, Li X, Sundquist J, Sundquist K. Age- and gender-specific familial risks for venous thromboembolism: a nationwide epidemiological study based on hospitalizations in Sweden. Circulation 2011; 124: 1012-1020.
    CrossrefPubMedGoogle Scholar
  • 8 Prandoni P, Prins MH, Ghirarduzzi A. et al. Family history of venous thrombosis or sudden death as a risk factor for venous thromboembolism. Thromb Haemost 2012; 107: 1191-1192.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 9 Stratton MR, Rahman N. The emerging landscape of breast cancer susceptibility. Nat Genet 2008; 40: 17-22.
    CrossrefPubMedGoogle Scholar
  • 10 Sorensen HT, Riis AH, Diaz LJ. et al. Familial risk of venous thromboembolism - a nationwide cohort study. J Thromb Haemost 2010; 9: 320-324.
    PubMedGoogle Scholar
  • 11 Rossi E, Ciminello A, Za T. et al. In families with inherited thrombophilia the risk of venous thromboembolism is dependent on the clinical phenotype of the proband. Thromb Haemost 2011; 106: 646-654.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 12 Villani M, Tiscia GL, Margaglione M. et al. Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias. J Thromb Haemost 2012; 10: 223-228.
    CrossrefPubMedGoogle Scholar
  • 13 McRae S, Tran H, Schulman S. et al. Effect of patient’s sex on risk of recurrent venous thromboembolism: a meta-analysis. Lancet 2006; 368: 371-378.
    CrossrefPubMedGoogle Scholar
  • 14 Douketis J, Tosetto A, Marcucci M. et al. Risk of recurrence after venous thromboembolism in men and women: patient level meta-analysis. Br Med J 2011; 342: d813.
    CrossrefPubMedGoogle Scholar
  • 15 Charchar FJ, Tomaszewski M, Lacka B. et al. Association of the human Y chromosome with cholesterol levels in the general population. Arterioscler Thromb Vasc Biol 2004; 24: 308-312.
    CrossrefPubMedGoogle Scholar
  • 16 Turner ME, Farkas J, Dunmire J. et al. Which Sry locus is the hypertensive Y chromosome locus?. Hypertension 2009; 53: 430-435.
    CrossrefPubMedGoogle Scholar
  • 17 Charchar FJ, Bloomer LDS, Barnes TA. et al. Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome. Lancet 2012; 379: 915-922.
    CrossrefPubMedGoogle Scholar
  • 18 Lemos B, Araripe LO, Hartl DL. Polymorphic Y chromosomes harbor cryptic variation with manifold functional consequences. Science 2008; 319: 91-93.
    CrossrefPubMedGoogle Scholar
  • 19 Spyropoulos AC, McGinn T, Khorana A. The use of weighted and scored risk assessment models for venous thromboembolism. Thromb Haemost 2012; 108: 1072-1076.
    Article in Thieme ConnectPubMedGoogle Scholar
  • 20 Kyrle PA, Eichinger S. Clinical scores to predict recurrence risk of venous thromboembolism. Thromb Haemost 2012; 108: 1061-1064.
    Article in Thieme ConnectPubMedGoogle Scholar