Skip to main content
Log in

Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism

  • Review
  • Published:
European Journal of Pediatrics Aims and scope Submit manuscript

Abstract

Childhood thrombo-embolism is mostly the result of inherited thrombophilia or vascular insults combined with risk factors such as peripartal asphyxia, fetopathia diabetica, exsiccosis, septicaemia, central lines, congenital heart disease, cancer, trauma, surgery or elevated antiphospholipid antibodies. Inherited thrombophilia includes mainly defects of the protein C pathway, resistance to activated protein C, protein C or protein S deficiency. Resistance to activated protein C, in the majority of cases caused by the point mutation Arg 506 Gln of the factor V gene, has emerged as the most important hereditary cause of thrombo-embolism in adults and children. However, since an acquired risk of thrombo-embolic complications frequently masks the inherited deficiency in affected children, children with thrombo-embolism should have adequate laboratory evaluation for inherited coagulation disorders, especially the protein C pathway. Until more data on childhood thrombo-embolism are available, treatment recommendations will continue to be extrapolated from guidelines for adults.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

Abbreviations

APC :

activated protein C

APCR :

resistance to the anticoagulatory effect of protein C

aPTT :

activated partial thromboplastin time

C4bB :

C4b binding protein

FFP :

fresh frozen plasma

PC :

protein C

PS :

protein S

TF :

tissue factor

References

  1. Alessi MC, Aillaud MF, Paut O, Roquelaure B, Alhenc-Gelas M, Pellissier MC, Ghanen N, Juhan-Vague I (1996) Purpura fulminans in a patient homozygous for a mutation in the protein C gene — prenatal diagnosis in a subsequent pregnancy. Thromb Haemost 75:520–521

    Google Scholar 

  2. Allaart CF, Poort S, Rosendal F, Reitsma P, Bertina R (1993) Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect. Lancet 341:134–138

    Google Scholar 

  3. Amer L, Kisiel W, Searles RP, Williams RC Jr (1990) Impairment of the protein C anticoagulant pathway in a patient with systemic lupus erythematosus, anticardiolipin antibodies and thrombosis. Thromb Res 57:247–258

    Google Scholar 

  4. Andrew M (1995) Developmental hemostasis: relevance to thromboembolic complications in pediatric patients. Thromb Haemost 74:415–425

    Google Scholar 

  5. Andrew M, Paes B, Milner R, Johnston M (1990) Development of the hemostatic system in the neonate and young infant. Am J Pediatr Hematol Oncol 12:95–104

    Google Scholar 

  6. Andrew M, Vegh P, Johnston M, Bowker J, Ofosu F, Mitchell L (1992) Maturation of the hemostatic system during childhood. Blood 80:1998–2005

    Google Scholar 

  7. Andrew M, David M, Adams M (1993) Venous thromboembolic complications in children. J Pediatr 123:337–346

    Google Scholar 

  8. Arav-Bogner R, Reif S, Bujanover Y (1995) Portal vein thrombosis caused by protein C and protein S deficiency associated with cytomegalovirus infection. J Pediatr 126:586–588

    Google Scholar 

  9. Arnout J, Vanrusselt M, Vermylen J (1995) Resistance to activated protein C in a population of patients with antiphospholipid antibodies. Thromb Haemost 73:1275

    Google Scholar 

  10. Auberger K (1992) Evaluation of a new protein C concentrate and comparison of protein C assays in a child with congenital protein C deficiency. Ann Hematol 64:146–151

    Google Scholar 

  11. Baliga V, Thwaites R, Tillyer ML, Minford A, Parapia L, Allgrove J (1995) Homozygous protein C deficiency — management with protein C concentrate. Eur J Pediatr 154:534–535

    Google Scholar 

  12. Bandello F, D'Angelo SV, Parlavecchia M, Tavola A, Valle PD, Brancato R, D'Angelo A (1994) Hypercoagulability and high lipoprotein (a) levels in patients with central retinal vein occlusion. Thromb Haemost 72:39–43

    Google Scholar 

  13. Bertina RM, Ploos Van Amstel HK, Wijngaarden A van, Coenen J, Leemhuis MP, Deutz Terlouw PP, Linden IK van der, Reitsma PH (1990) Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460. Blood 76:538–548

    Google Scholar 

  14. Bertina RM, Koeleman BPC, Koster T, Rosendaal FR, Dirven RJ, Ronde H de, Velden PA van der, Reitsma PH (1994) Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 369:64–67

    Google Scholar 

  15. Bick RL, Baker WF (1994) The antiphospholipid and thrombosis syndromes. Med Clin North Am 78:667–684

    Google Scholar 

  16. Bick R, Ucar K (1992) Hypercoagulability and thrombosis. Hematol Oncol Clin North Am 6:1421–1429

    Google Scholar 

  17. Bovill EG, Bauer KA, Dickermann JD, Callas P, West B (1989) The clinical spectrum of heterozygous protein C deficiency in a large New England kindred. Blood 73:712–717

    Google Scholar 

  18. Cooper PC, Hampton KK, Makris M, Abuzenadah A, Paul B, Preston FE (1994) Further evidence that activated protein C resistance can be misdiagnosed as inherited functional protein S deficiency. Br J Haematol 88:201–203

    Google Scholar 

  19. Dahlbäck B (1986) Inhibition of protein C cofactor function of human and bovine protein S by C4b-binding protein. J Biol Chem 261:12022–12027

    Google Scholar 

  20. Dahlbäck B (1991) Protein S and C4b-binding protein: components involved in the regulation of the protein C anticoagulant system. Thromb Haemost 66:49–61

    Google Scholar 

  21. Dahlbäck B (1995) New molecular insights into the genetics of thrombophilia. Resistance to activated protein C caused by Arg 506 to Gln mutation in factor V as a pathogenetic risk factor. Thromb Haemost 74:139–148

    Google Scholar 

  22. Dahlbäck B (1995) Factor V gene mutation causing inherited resistance to activated protein C as a basis for venous thromboembolism. J Int Med 237:221–227

    Google Scholar 

  23. Dahlbäck B, Carlsson M (1991) Factor VIII defect associated with familial thrombophilia. Thromb Haemost 65:658

    Google Scholar 

  24. Dahlbäck B, Carlsson M, Svensson PJ (1993) Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 90:1004–1008

    Google Scholar 

  25. D'Angelo SV, Mazzola G, Valle PD, Testa S, Pattarini E, D'Angelo A (1995) Variable interference of activated protein C resistance in the measurement of protein S activity by commercial assays. Thromb Res 77:375–378

    Google Scholar 

  26. David M, Andrew M (1993) Venous thromboembolic complications in children. J Pediatr 123:337–346

    Google Scholar 

  27. David M, Manco-Johnson M, Andrew M (1995) Diagnosis and treatment of venous thromboembolism in children and adolescents. On behalf of the subcommittee on perinatal haemostasis of the scientific and standardization committee of the ISTH. Thromb Haemost 74:791–792

    Google Scholar 

  28. Dreyfuß M, Magny JF, Bridey F, Schwarz HP, Planche C, Dehan M, Tchernia G (1991) Treatment of homozygous protein C deficiency and neonatal purpura fulminans with purified protein C concentrate. N Engl J Med 325:1565–1568

    Google Scholar 

  29. Edenbrandt CM, Lindwall A, Wydro R, Stenflo J (1990) Molecular analysis of the gene for vitamin K-dependent protein S and its pseudogene. Cloning and partial gene organization. Biochemistry 29:7861–7868

    Google Scholar 

  30. Esmon CT (1989) The role of protein C and thrombomodulin in the regulation of blood coagulation. J Biol Chem 264:4743–4749

    Google Scholar 

  31. Faioni EM, Boyer-Neumann C, Franchi F, Wolf M, Meyer D, Mannucci P (1994) Another protein S functional assay is sensitive to resistance to activated protein C. Thromb Haemost 72:643–651

    Google Scholar 

  32. Foster DC, Yoshitake S, Davie EW (1985) The nucleotide sequence of the gene for human protein C. Proc Natl Acad Sci USA 82:4673–4677

    Google Scholar 

  33. Gandrille S, Borgel D, Eschwege-Gufflet V, Aillaud MF, Dreyfuß M, Matheron C, Gaussem P, Abgrall JF, Jude B, Sie P, Toulon P, Aiach M (1995) Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene. Blood 85:130–139

    Google Scholar 

  34. Gladson CL, Scharrer I, Hach V, Beck KM, Griffin JH (1988) The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis. Thromb Haemost 59:18–22

    Google Scholar 

  35. Göbel U (1994) Inherited or acquired disorders of blood coagulation in children with neurovascular complications. Neuropediatrics 25:4–7

    Google Scholar 

  36. Gomez E, Ledford MR, Pegelow CH, Reitsma PH, Bettina RM (1994) Homozygous protein S deficiency caused by one base pair deletion that leads to a stop codon in exon III of the protein S gene. Thromb Haemost 71:723–726

    Google Scholar 

  37. Gurewich V, Pannell R, Louie S, Kelley P, Suddith RL, Greenlee R (1984) Effective and fibrin-specific clot lysis by a zymogen precursor form of urokinase (pro-urokinase). A study in vitro and in two animal species. J Clin Invest 73:1731–1739

    Google Scholar 

  38. Hayashi T, Nishioka J, Shigekiyo T, Saito S, Suzuki K (1994) Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S. Blood 83:683–690

    Google Scholar 

  39. Haverkate F, Samama M (1995) Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC subcommittee on fibrinogen. Thromb Haemost 73:151–161

    Google Scholar 

  40. Heijboer H, Brandjed D, Buller H, Sturk A, Wouter ten Cate J (1990) Deficiencies of coagulation inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis. N Engl J Med 323:1512–1516

    Google Scholar 

  41. Hirsch J (1991) Oral anticoagulant drugs. N Engl J Med 342:1865–1875

    Google Scholar 

  42. Ichinose A, Fujikawa K, Suyama T (1986) The activation of prourokinase by plasma kallikrein and ist inactivation by thrombin. J Biol Chem 261:3486–3489

    Google Scholar 

  43. Jaffe EA (1991) Endothelial structure and function. In: Hoffman R, Benz EJ Jr, Shattil SJ, Furie B, Cohen HJ (eds) Hematology, basic principles and practice. Churchill-Livingstone, New York, pp 1198–1213

    Google Scholar 

  44. Kluft C (1994) Constitutive synthesis of tissue-type plasminogen activator (tPA) and plasminogen activator inhibitor type 1 (PAT-1): conditions and therapeutic targets. Fibrinolysis 8(2):1–7

    Google Scholar 

  45. Kodish E, Potter C, Kirschbaum N, Foster P (1995) Activated protein C resistance in a neonate with venous thrombosis. J Pediatr 127:645–648

    Google Scholar 

  46. Koster T, Rosendaal FR, Ronde H de, Briet E, Vandenbroucke JP, Bertina RM (1993) Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study. Lancet 342:1503–1506

    Google Scholar 

  47. Levy M, Benson L, Burrows PE, Bentur Y, Strong DK, Smith J, Johnson D, Jacobson S, Koren G (1991) Tissue plasminogen activator for the treatment of thromboembolism in infants and children. J Pediatr 118:467–472

    Google Scholar 

  48. Mahn J, Laurell M, Nilsson I, Dahlbäck B (1992) Thromboembolic disease — critical evaluation of laboratory investigation. Thromb Haemost 8:7–13

    Google Scholar 

  49. Mannucci PM, Tripodi A (1987) Laboratory screening of inherited thrombotic syndromes. Thromb Haemost 57:247–251

    Google Scholar 

  50. Marlar RA, Neumann A (1990) Neonatal purpura fulminans due to homozygous protein C or S deficiencies. Sem Thromb Hemost 16:299–309

    Google Scholar 

  51. Miletich J, Sherman L, Broze G (1987) Absence of thrombosis in subjects with heterozygous protein C deficiency. N Engl J Med 317:991–996

    Google Scholar 

  52. Müller EM, Ehrenthal W, Hafner G, Schranz D (1996) Purpura fulminans in severe congenital protein C deficiency: monitoring of treatment with protein C concentrate. Eur J Pediatr 155:20–25

    Google Scholar 

  53. Nowak-Göttl U, Schwabe D, Schneider W, Schlösser R, Kreuz W (1992) Thrombolysis with recombinant tissue type plasminogen activator in renal venous thrombosis in infancy. Lancet 340:1105

    Google Scholar 

  54. Nowak-Göttl U, Funk M, Mosch G, Wegerich B, Kornhuber B, Breddin HK (1994) Univariate tolerance regions for fibrinogen, antithrombin III, protein C, protein S, plasminogen and α2-antiplasmin in children using the new automated coagulation laboratory (ACL) method. Klin Pädiatr 206:437–439

    Google Scholar 

  55. Nowak-Göttl U, Ashka I, Koch HG, Boos J, Dockhorn-Dworniczak B, Deufel T, Jürgens H, Kohlhase B, Kuhn N, Laupert A, Rath B, Wolff JEA, Schneppenheim R (1995) Resistance to activated protein C (APCR) in children with acute lymphoblastic leukaemia — the need for a prospective multicentre study. Blood Coag Fibrinol 6:761–764

    Google Scholar 

  56. Nowak-Göttl U, Koch HG, Aschka I, Kohlhase B, Vielhaber H, Kurlemann G, Oleszuk-Rasche K, Kehl HG, Jürgens H, Schneppenheim R (1996) Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism. Br J Haematol 92:992–998

    Google Scholar 

  57. Nowak-Göttl U, Kohlhase B, Vielhaber H, Aschka I, Schneppenheim R, Jürgens H (1996) APC resistance in neonates and infants: adjustment of the aPTT-based method. Thromb Res 81:665–670

    Google Scholar 

  58. Nuss R, Hys T, Manco-Johnson M (1995) Childhood thrombosis. Pediatrics 96:291–294

    Google Scholar 

  59. Petäjä J, Jalanko H, Holmberg C, Kinmmen S, Syrjälä (1995) Resistance to activated protein C as an underlying cause of recurrent venous thrombosis during relapsing nephrotic syndrome. J Pediatr 127:103–105

    Google Scholar 

  60. Ploos Van Amstel HK, Zanden AL van der, Bakker E, Reitsma PH, Bettina RM (1987) Two genes homologous with human protein S cDNA are located on chromosome 3. Thromb Haemost 58:982–987

    Google Scholar 

  61. Ploos Van Amstel HK, Huisman MV, Reitsma PH, Wouter ten Cate J, Bettina RM (1989) Partial protein S gene deletion in a family with hereditary thrombophilia. Blood 73:479–483

    Google Scholar 

  62. Ploos Van Amstel HK, Reitsma PH, Bertina RM (1989) The human protein S locus: identification of the PS alpha gene as a site of liver protein S messenger RNA synthesis. Biochem Biophys Res Commun 157:1033–1038

    Google Scholar 

  63. Ploos Van Amstel HK, Reitsma PH, Hamulyak K, Smulders CE de, Mannucci PM, Bettina RM (1989) A mutation in the protein S pseudogene is linked to protein S deficiency in a thrombophilic family. Thromb Haemost 62:897–901

    Google Scholar 

  64. Ploos Van Amstel HK, Reitsma PH, Logt CP van der, Bertina RM (1990) Intron-exon organisation of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolution. Biochemistry 29:7853–7861

    Google Scholar 

  65. Plutzky J, Hoskins JA, Long GL, Crabtree GR (1986) Evolution and organization of the human protein C gene. Proc Natl Acad Sci USA 83:546–550

    Google Scholar 

  66. Reitsma PH, Poort SR, Allaart CF, Briet E, Bettina RM (1991) The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: Heterogenity and founder effects. Blood 78:890–894

    Google Scholar 

  67. Reitsma PH, Ploos Van Amstel HK, Bertina RM (1994) Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I. J Clin Invest 93:486–492

    Google Scholar 

  68. Reitsma PH, Bernardi F, Doig RG, Gandrille S, Greengard JS, Ireland H, Krawczak M, Lind B, Long GL, Poort SR, Saito H, Sala N, Witt I, Cooper DN (1995) Protein C deficiency: a database of mutations, 1995 update. Thromb Haemost 73:786–879

    Google Scholar 

  69. Rodgers L, Luther C. Streptokinase therapy for deep vein thrombosis: a comprehensive review of the English literature. Am J Med 88:389–395

  70. Rosenbaum T, Rammos S, Kniemeyer HW, Göbel U (1993) Extended deep vein and inferior vena cava thrombosis in a 15-year-old boy: successful lysis with recombinant tissue type plasminogen activator 2 weeks after onset symptoms. Eur J Pediatr 152:978–980

    Google Scholar 

  71. Ryan CA, Andrew M (1992) Failure of thrombolytic therapy in four children with extensive thrombosis. Am J Dis Child 146:187–193

    Google Scholar 

  72. Schmidel DK, Nelson RM, Broxson EH, Comp PC, Marlar RA, Long GL (1991) A 5.3-kb deletion including exon XIII of the protein S a gene occurs in two protein S-deficient families. Blood 77:551–559

    Google Scholar 

  73. Schmidt B, Andrew M (1995) Neonatal thrombosis: report of a prospective Canadian and international registry. Pediatrics 96:939–943

    Google Scholar 

  74. Schwabe D, Schlösser R, Auberger K, Kries R von, Nowak-Göttl U (1996) Thrombolyse mit rt-PA im 1. Lebensjahr. Hämostaseologie (in press)

  75. Shen L, Dahlbäck B (1994) Factor V and protein C in degradation of factor VIIIa. J Biol Chem 269:18735–18738

    Google Scholar 

  76. Simioni P, De Ronde H, Prandoni P, Saladini M, Bertina RM, Girolami A (1995) Ischemic stroke in young patients with activated protein C resistance. A report of three cases belonging to three different kindreds. Stroke 26:885–890

    Google Scholar 

  77. Svensson PJ, Dahlbäck B (1994) Resistance to activated protein C as a basis for venous thrombosis. N Engl J Med 330:517–522

    Google Scholar 

  78. Taberno M, Tomas J, Alberca I, Orfao A, Borrasca A, Vincente V (1991) Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis. Am J Hematol 36:249–254

    Google Scholar 

  79. Uziel Y, Laxer RM, Blaser S, Andrew M, Schneider R, Silverman ED (1995) Cerebral vein thrombosis in childhood systemic lupus erythematosus. J Pediatr 126:722–727

    Google Scholar 

  80. Vielhaber H, Kohlhase B, Kehl HG, Fliedner M, Kececioglu D, Dockhorn-Dworniczak B, Kehrel B, Veltmann H, Vogt J, Nowak-Göttl U (1996) Flush heparin during cardiac catherisation prevents long-term coagulation activation in children without APC-resistance — preliminary results. Thromb Res 81:651–656

    Google Scholar 

  81. Whitlock J, Janco R, Phillips J (1989) Inherited hypercoagulable states in children. Am J Pediatr Hematol Oncol 11:170–173

    Google Scholar 

  82. Wiman B, Hamsten A (1990) The fibrinolytic enzyme system and its role in the etiology of thromboembolic disease. Sem Thromb Haemost 16:207–214

    Google Scholar 

  83. Zenz W, Muntean W, Gallistl S, Leschnik B, Beitzke A (1994) Inherited resistance to activated protein C in a boy with multiple thromboses in early infancy. Eur J Pediatr 154:285–288

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nowak-Göttl, U., Auberger, K., Göbel, U. et al. Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism. Eur J Pediatr 155, 921–927 (1996). https://doi.org/10.1007/BF02282879

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02282879

Key words

Navigation