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Semin Thromb Hemost 2013; 39(06): 607-612
DOI: 10.1055/s-0033-1349224
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Parahemophilia: New Insights into Factor V Deficiency

Nabil Thalji
1   Division of Hematology, Department of Pediatrics, The Children's Hospital of Philadelphia, Perelman School of Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania
,
Rodney M. Camire
1   Division of Hematology, Department of Pediatrics, The Children's Hospital of Philadelphia, Perelman School of Medicine, The University of Pennsylvania, Philadelphia, Pennsylvania
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Publikationsdatum:
26. Juli 2013 (online)

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Abstract

Blood coagulation factor V (FV) plays a pivotal role in blood coagulation. It is found in both plasma and in platelets and has a profound impact on thrombin generation. Deficiency of this clotting factor due to inherited or acquired conditions results in a broad spectrum of bleeding symptoms. Surprisingly however, some patients with undetectable levels of FV experience relatively mild bleeding. The aim of this review is to highlight this rare coagulation factor disorder and touch upon its clinical manifestations, diagnosis, and treatment. Furthermore, recent advances that shed new light on the importance of platelet FV and other modifiers which influence bleeding tendencies in severe FV deficiency will be discussed.

Keywords

factor V - factor V deficiency - hemostasis - bleeding phenotype
 

  • References

  • 1 Owren PA. Parahaemophila: haemorrhagic diathesis due to absence of a previously unknown clotting factor. Lancet 1947; 249: 446-448
    CrossrefPubMedSuche in Google Scholar
  • 2 Stormorken H. The discovery of factor V: a tricky clotting factor. J Thromb Haemost 2003; 1 (2) 206-213
    CrossrefPubMedSuche in Google Scholar
  • 3 Mann KG, Kalafatis M. Factor V: a combination of Dr Jekyll and Mr Hyde. Blood 2003; 101 (1) 20-30
    CrossrefPubMedSuche in Google Scholar
  • 4 Camire RM, Bos MHA. The molecular basis of factor V and VIII procofactor activation. J Thromb Haemost 2009; 7 (12) 1951-1961
    CrossrefPubMedSuche in Google Scholar
  • 5 Cripe LD, Moore KD, Kane WH. Structure of the gene for human coagulation factor V. Biochemistry 1992; 31 (15) 3777-3785
    CrossrefPubMedSuche in Google Scholar
  • 6 Kane WH, Davie EW. Cloning of a cDNA coding for human factor V, a blood coagulation factor homologous to factor VIII and ceruloplasmin. Proc Natl Acad Sci U S A 1986; 83 (18) 6800-6804
    CrossrefPubMedSuche in Google Scholar
  • 7 Jenny RJ, Pittman DD, Toole JJ , et al. Complete cDNA and derived amino acid sequence of human factor V. Proc Natl Acad Sci U S A 1987; 84 (14) 4846-4850
    CrossrefPubMedSuche in Google Scholar
  • 8 Kane WH, Ichinose A, Hagen FS, Davie EW. Cloning of cDNAs coding for the heavy chain region and connecting region of human factor V, a blood coagulation factor with four types of internal repeats. Biochemistry 1987; 26 (20) 6508-6514
    CrossrefPubMedSuche in Google Scholar
  • 9 Wilson DB, Salem HH, Mruk JS, Maruyama I, Majerus PW. Biosynthesis of coagulation Factor V by a human hepatocellular carcinoma cell line. J Clin Invest 1984; 73 (3) 654-658
    CrossrefPubMedSuche in Google Scholar
  • 10 Mazzorana M, Baffet G, Kneip B, Launois B, Guguen-Guillouzo C. Expression of coagulation factor V gene by normal adult human hepatocytes in primary culture. Br J Haematol 1991; 78 (2) 229-235
    CrossrefPubMedSuche in Google Scholar
  • 11 Tracy PB, Eide LL, Bowie EJW, Mann KG. Radioimmunoassay of factor V in human plasma and platelets. Blood 1982; 60 (1) 59-63
    PubMedSuche in Google Scholar
  • 12 Mann KG, Nesheim ME, Church WR, Haley PE, Krishnaswamy S. Surface-dependent reactions of the vitamin K-dependent enzyme complexes. Blood 1990; 76 (1) 1-16
    PubMedSuche in Google Scholar
  • 13 Asselta R, Peyvandi F. Factor V deficiency. Semin Thromb Hemost 2009; 35 (4) 382-389
    Thieme ConnectPubMedSuche in Google Scholar
  • 14 Duckers C, Simioni P, Rosing J, Castoldi E. Advances in understanding the bleeding diathesis in factor V deficiency. Br J Haematol 2009; 146 (1) 17-26
    CrossrefPubMedSuche in Google Scholar
  • 15 Cui J, O'Shea KS, Purkayastha A, Saunders TL, Ginsburg D. Fatal haemorrhage and incomplete block to embryogenesis in mice lacking coagulation factor V. Nature 1996; 384 (6604) 66-68
    CrossrefPubMedSuche in Google Scholar
  • 16 Mannucci PM, Peyvandi F, Franchini M, Rare inherited coagulation disorders other than hemophilia. In: Marder VJ, Aird WC, Bennett JS, Schulman S, White GC. , eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2013: 684-692
    Suche in Google Scholar
  • 17 Acharya SS, Coughlin A, Dimichele DM. North American Rare Bleeding Disorder Study Group. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2 (2) 248-256
    CrossrefPubMedSuche in Google Scholar
  • 18 Zhang B. Recent developments in the understanding of the combined deficiency of FV and FVIII. Br J Haematol 2009; 145 (1) 15-23
    CrossrefPubMedSuche in Google Scholar
  • 19 Zhang B, Cunningham MA, Nichols WC , et al. Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex. Nat Genet 2003; 34 (2) 220-225
    CrossrefPubMedSuche in Google Scholar
  • 20 Nichols WC, Seligsohn U, Zivelin A , et al. Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping. J Clin Invest 1997; 99 (4) 596-601
    CrossrefPubMedSuche in Google Scholar
  • 21 Neerman-Arbez M, Antonarakis SE, Blouin JL , et al. The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103. Am J Hum Genet 1997; 61 (1) 143-150
    CrossrefPubMedSuche in Google Scholar
  • 22 Franchini M, Lippi G. Acquired factor V inhibitors: a systematic review. J Thromb Thrombolysis 2011; 31 (4) 449-457
    CrossrefPubMedSuche in Google Scholar
  • 23 Ortel TL. Clinical and laboratory manifestations of anti-factor V antibodies. J Lab Clin Med 1999; 133 (4) 326-334
    CrossrefPubMedSuche in Google Scholar
  • 24 Weiss HJ. Impaired platelet procoagulant mechanisms in patients with bleeding disorders. Semin Thromb Hemost 2009; 35 (2) 233-241
    Thieme ConnectPubMedSuche in Google Scholar
  • 25 Blavignac J, Bunimov N, Rivard GE, Hayward CP. Quebec platelet disorder: update on pathogenesis, diagnosis, and treatment. Semin Thromb Hemost 2011; 37 (6) 713-720
    Thieme ConnectPubMedSuche in Google Scholar
  • 26 ThoMurray JM, Rand MD, Egan JO, Murphy S, Kim HC, Mann KG. Factor VNew Brunswick: Ala221-to-Val substitution results in reduced cofactor activity. Blood 1995; 86 (5) 1820-1827
    PubMedSuche in Google Scholar
  • 27 Paraboschi EM, Kayiran SM, Özbek N , et al. Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency. Haemophilia 2012; 18 (2) 205-210
    CrossrefPubMedSuche in Google Scholar
  • 28 Lak M, Sharifian R, Peyvandi F, Mannucci PM. Symptoms of inherited factor V deficiency in 35 Iranian patients. Br J Haematol 1998; 103 (4) 1067-1069
    CrossrefPubMedSuche in Google Scholar
  • 29 Delev D, Pavlova A, Heinz S, Seifried E, Oldenburg J. Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency. Haemophilia 2009; 15 (5) 1143-1153
    CrossrefPubMedSuche in Google Scholar
  • 30 Dahlbäck B, Villoutreix BO. Molecular recognition in the protein C anticoagulant pathway. J Thromb Haemost 2003; 1 (7) 1525-1534
    CrossrefPubMedSuche in Google Scholar
  • 31 Simioni P, Scudeller A, Radossi P , et al. “Pseudo homozygous” activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds. Thromb Haemost 1996; 75 (3) 422-426
    PubMedSuche in Google Scholar
  • 32 Camire RM, Pollak ES, Kaushansky K, Tracy PB. Secretable human platelet-derived factor V originates from the plasma pool. Blood 1998; 92 (9) 3035-3041
    PubMedSuche in Google Scholar
  • 33 Thomassen MC, Castoldi E, Tans G , et al. Endogenous factor V synthesis in megakaryocytes contributes negligibly to the platelet factor V pool. Haematologica 2003; 88 (10) 1150-1156
    PubMedSuche in Google Scholar
  • 34 Gould WR, Simioni P, Silveira JR, Tormene D, Kalafatis M, Tracy PB. Megakaryocytes endocytose and subsequently modify human factor V in vivo to form the entire pool of a unique platelet-derived cofactor. J Thromb Haemost 2005; 3 (3) 450-456
    CrossrefPubMedSuche in Google Scholar
  • 35 Bouchard BA, Williams JL, Meisler NT, Long MW, Tracy PB. Endocytosis of plasma-derived factor V by megakaryocytes occurs via a clathrin-dependent, specific membrane binding event. J Thromb Haemost 2005; 3 (3) 541-551
    CrossrefPubMedSuche in Google Scholar
  • 36 Bouchard BA, Meisler NT, Nesheim ME, Liu CX, Strickland DK, Tracy PB. A unique function for LRP-1: a component of a two-receptor system mediating specific endocytosis of plasma-derived factor V by megakaryocytes. J Thromb Haemost 2008; 6 (4) 638-644
    CrossrefPubMedSuche in Google Scholar
  • 37 Gould WR, Silveira JR, Tracy PB. Unique in vivo modifications of coagulation factor V produce a physically and functionally distinct platelet-derived cofactor: characterization of purified platelet-derived factor V/Va. J Biol Chem 2004; 279 (4) 2383-2393
    PubMedSuche in Google Scholar
  • 38 Duckers C, Simioni P, Spiezia L , et al. Residual platelet factor V ensures thrombin generation in patients with severe congenital factor V deficiency and mild bleeding symptoms. Blood 2010; 115 (4) 879-886
    CrossrefPubMedSuche in Google Scholar
  • 39 Castoldi E, Duckers C, Radu C , et al. Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma. J Thromb Haemost 2011; 9 (5) 959-968
    CrossrefPubMedSuche in Google Scholar
  • 40 Yang TL, Cui J, Taylor JM, Yang A, Gruber SB, Ginsburg D. Rescue of fatal neonatal hemorrhage in factor V deficient mice by low level transgene expression. Thromb Haemost 2000; 83 (1) 70-77
    PubMedSuche in Google Scholar
  • 41 Mann KG. How much factor V is enough?. Thromb Haemost 2000; 83 (1) 3-4
    PubMedSuche in Google Scholar
  • 42 Duckers C, Simioni P, Spiezia L , et al. Low plasma levels of tissue factor pathway inhibitor in patients with congenital factor V deficiency. Blood 2008; 112 (9) 3615-3623
    CrossrefPubMedSuche in Google Scholar
  • 43 Talbot K, Song J, Hewitt J , et al. A novel compensating mechanism for homozygous coagulation factor V deficiency suggested by enhanced activated partial thromboplastin time after reconstitution with normal factor V. Br J Haematol 2010; 151 (2) 198-200
    CrossrefPubMedSuche in Google Scholar