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Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy.

Abstract
Bleeding complications are the most common and unwanted side-effect of oral anticoagulant therapy. We report three patients in whom mutations in the factor IX (FIX) propeptide were found to cause severe bleeding during coumarin therapy. Strikingly, the bleeding occurred within the therapeutic ranges of the prothrombin time (PT) and international normalized ratio (INR). In all three patients coumarin therapy caused an unusually selective decrease of FIX activity (FIX:C) to levels below 1-3%. Upon withdrawal of coumarin, FIX:C increased to subnormal or normal values of 55%, 85% and 125%, respectively. Analysis of the FIX gene revealed two different missense mutations affecting the Ala-10 residue in the propeptide coding region: Ala[GCC] to Val[GTC] in two patients and Ala[GCC] to Thr[ACC] in one patient. No further mutation was detected by screening 195 random blood donors for mutations at Ala-10, thus excluding a frequent polymorphism at this position. The mutation in the FIX propeptide at a position which is essential for the carboxylase recognition site causes a reduced affinity of the carboxylase enzyme to the propeptide. This effect leads to an impaired carboxylase epoxidase reaction which is decisively triggered by the vitamin K concentration. Determination of FIX and APTT in addition to PT and INR is therefore recommended in coumarin-treated patients with an uncommon bleeding pattern.
AuthorsJ Oldenburg, E M Quenzel, U Harbrecht, A Fregin, W Kress, C R Müller, H J Hertfelder, R Schwaab, H H Brackmann, P Hanfland
JournalBritish journal of haematology (Br J Haematol) Vol. 98 Issue 1 Pg. 240-4 (Jul 1997) ISSN: 0007-1048 [Print] England
PMID9233593 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anticoagulants
  • Peptide Fragments
  • Factor IX
Topics
  • Administration, Oral
  • Adult
  • Aged
  • Anticoagulants (adverse effects)
  • Exons (genetics)
  • Factor IX (genetics)
  • Hemorrhage (chemically induced, genetics)
  • Humans
  • Mutation
  • Peptide Fragments (genetics)

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