Severe hemophilia with mild bleeding phenotype: Molecular characterization and global coagulation profile

E. Santagostino, M. E. Mancuso, A. Tripodi, V. Chantarangkul, M. Clerici, I. Garagiola, P. M. Mannucci

Research output: Contribution to journalArticlepeer-review


Background: Patients with severe hemophilia may show very varied bleeding tendencies, and the reasons for this heterogeneous clinical expression are unclear. The factor VIII/FIX genotype is the main determinant of the residual factor activity; however, different bleeding phenotypes have also been reported in patients sharing the same mutation. Such global coagulation tests as thrombin generation assays are tools with which to investigate different coagulation profiles among severe hemophiliacs. Objectives, patients and methods: This case-control study was aimed at comprehensively evaluating the role of genotype and endogenous thrombin potential (ETP) as predictors of the clinical phenotype in severe hemophiliacs with an extremely mild bleeding tendency (cases, n = 22), in comparison with those showing a typical bleeding tendency (controls, n = 50). Results: Cases were more frequently affected by hemophilia B than by hemophilia A, and showed a lower incidence of severe FVIII/FIX gene defects (referred to as null mutations), higher FVIII and FIX antigen levels and higher ETP values in platelet-rich plasma than controls (P <0.05). By multivariate logistic regression, only non-null mutations were confirmed as an independent predictor of a mild clinical phenotype. Conclusions: These results indicate that non-null mutations represent the main determinant of the bleeding tendency, and that ETP measurement in platelet-rich plasma is able to identify severe hemophiliacs with a mild clinical phenotype.

Original languageEnglish
Pages (from-to)737-743
Number of pages7
JournalJournal of Thrombosis and Haemostasis
Issue number4
Publication statusPublished - Apr 2010


  • Endogenous thrombin potential
  • Genotype
  • Hemophilia A
  • Hemophilia B
  • Phenotype

ASJC Scopus subject areas

  • Hematology


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