PubMed · 2004 · 74 citations · 15 references
MedicineHematologyHemostasisMedical GeneticsMolecular DiagnosticsBleeding DisordersCoagulation AbnormalitiesCoagulation DisordersCoagulation Factor DeficienciesHemostatic DisordersThrombosisBleedingBleeding Phenotype AssessmentHereditary Bleeding DisordersInherited Coagulation Factor DeficienciesRare Bleeding DisordersRare Coagulation Factor DeficienciesRecombinant Activated Factor ViiTissue Factor Pathway Inhibitor Deficiency
BACKGROUND AND OBJECTIVES: Inherited factor VII (FVII) deficiency is a rare bleeding disorder characterized by a poor relationship between reported FVII clotting activity (FVII:C) and bleeding tendency. Our study was aimed at defining biological parameters that are possibly predictive for bleeding risk in this condition. DESIGN AND METHODS: Forty-two FVII-deficient patients (FVII:C <30%) were classified into two opposite clinical groups defined as severe and non-or-mild bleeders. For each patient, plasma samples were collected and then investigated for FVII:C (using a sensitive method and human recombinant thromboplastin as the reagent), FVII antigen, activated FVII coagulant activity (FVIIa:C) and the free-form of tissue factor pathway inhibitor. RESULTS: None of these tests could be used as highly accurate predictors of bleeding. Nevertheless, both FVII:C and FVIIa:C differed significantly between the two clinical groups. Using ROC-curve analysis, two critical values of 8% and 3mIU/mL for FVII:C and FVIIa:C, respectively, could be proposed to discriminate between severe bleeders and non-or-mild bleeders. INTERPRETATION AND CONCLUSIONS: A highly accurate diagnostic test for predicting bleeding tendency in inherited FVII deficiency still eludes definition, highlighting the fact that factors other than FVII itself interfere with the expression of bleeding phenotypes in this condition. Nevertheless, potential critical values using sensitive FVII:C and FVIIa:C methods may be useful in clinical laboratories for FVII-deficient patients. Those patients with FVII:C levels higher than 8% FVII:C or FVIIa:C higher than 3 mIU/mL, with no other hemostatic defect, seem to have a minimal risk of severe bleeding. Extended clinical studies are needed to support these findings.
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Saulius Butenas, Cornelis van’t Veer, Kenneth G. Mann · Blood · 1999 · 381 citations
Medicine, Biochemistry, Hematology +17
The genetics of haemostasis: a twin study
Marlies de Lange, Harold Snieder, Robert A.S. Ariëns et al. · The Lancet · 2001 · 293 citations
Triplett Da, JT Brandt, MA Batard et al. · Blood · 1985 · 169 citations · Full text
Measurement of basal levels of factor VIIa in hemophilia A and B patients [see comments]
P Wildgoose, Yale Nemerson, L. L. Hansen et al. · Blood · 1992 · 164 citations · Full text