LEIDEN FACTOR V AND G2021 OA IN RECURRENT SPONTANEOUS ABORTION AND STILLBIRTH

Authors

  • Renata Zaccaria
  • Egle Couto
  • Ricardo Barini
  • Joyce Maria Annicchino-Bizzacchi
  • José Carlos Gama da Silva
  • João Luiz Pinto e Silva

Keywords:

spontaneous abortion, Leiden factor V, stillbirth, prothrombin, thrombophilia

Abstract

Objective
Fetal losses and other pregnancy complications have been associated with maternal thrombosis. Inherited thrombophilia factors are possible causes for these events. To evaluate the association between inherited thrombophilia and gestational losses

Methods
A retrospective cohort study included 42 women patients at the Hematology ambulatory, who were carriers of Leiden factor V (Group 1 ) and 94 women without this factor, patients at the Family Planning ambulatory (Group 2). Personal history of gestational losses and personal and familiar history of thromboembolic disease were Énvestigated on clinical charts and by phone interviews. Descriptive analyses were carried out by using frequency tables, and position and dispersion measurements. To check for associations or to compare proportions. the Chi-square or the Fisher exact tests were used

Results
There were no statistical differences between studied groups on the occurrence of stillbirth. In Group 1, of 109 pregnanctes, 26.6% ended as abortion. In Group 2, of 226 pregnancies, 9.6% ended as abortÊon (p<0.0001). Women from Group
1 had a higher prevalence of recurrent abortion and familiar history of thromboembolic events (p<0,0001 ). They were heterozygous Leiden factor V carriers, and three of them were also carriers of heterozygous G20210A mutation
in prothrombin gene

Conclusion
The frequency of spontaneous abortion and recurrent abortion was higher in carriers of inherited thrombophiIÊc factors, and these women showed a higher tendency to personal thromboembolic events.

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References

Rai R, Reagan L, Hadley E, Dave M, Cohen H. Second-trimester pregnancy loss is associated with activated protein C resistance. Br J Haematol. 1996; 92(2): 489-90.

Forastiero R, Martinuzzo M, Adamczuk Y, Iglesias Varela ML, Pombo G, Carreras LO. The combination of thrombophilic genotypes is associated with definite antiphospholipid syndromes. Haematologica. 2001; 86(7):735-41

Brenner B, MandeI H, Lanir N. Yonis J. Rothbart H Ohel G, Blumenfeld Z' Activated protein C resistance can be associated with recurrent fetal loss. Br J Haematol. 1997; 97(3):551-4.

Lane DA, Manucci PM, Bauer KA. Bertina RM, Bochkov NP, Boulyjenkov V, et al, Inherited thrombophilia: part 1. Thromb Haemost. 1996; 76(5):651-62

Arruda VR, Figueiredo MS, Biologia molecular para o hematologista clínico. Temas Hematol Clin. 1997; 187-99. Autor: indicar o volume e o fascículo

Bertina RM, Koeleman BP, Koster T. Rosendaal FR. Dirven RJ, Ronde H. et al, Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature. 1994; 369(6475):64-7.

Dalhbach B. Inherited thrombophilia: Resistance to activated protein C as a pathogenic factor of venous thromboembolism. Blood, 1995; 85(3):607-14.

Kujovich J, Goodnigt S. Factor V de Leiden Thrombophilia: Hereditary resistence to actived proteinC; factor V R506Q. Seattle: University of Washington; 1999

Foka ZJ, Lambropoulos AF. Saravelos H, Karas GB, Karavida A, Agorastos T, ef a/. Factor V Leiden and prothrombin G20210A mutations, but not methylene tetrahydrofolate reductase C677T, are associated with recurrent rniscarriages, Hum Reprod. 2000; 15(2)

-62

Dizon-Townson DS, Meline L. Nelson LM, Varner M. Ward K. Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction. Am J Obstet Gynecol. 1997; 177(2):402-5

Poort FE, Rosendal FR, Reitsma PH. Bertina RM. A common genetic variation in the 3“-unstralated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood. 1996; 88:3698-703

Kupferrninc MJ, Eldor A, Steinman N, Many A, Bar-Am A, Jaffa A, et al. Increased frequency of genetic thrornbofilia in women with complications of pregnancy. N Engl J Med. 1999; 340(1):9-13

Sambrook i, Fritsch EF, Maniaüs T. Molecular cloning A laboratory manual. 2nd ed, New York: Cold Spring Harbor; 1989

Couto E, Barini R, Annichino-Bizzacchi JM, Negrão P, Oliveira G. Comparative study of the frequency of thrombogenic factors in spontaneous aborting and fertile women. J Autoimmun. 2000; 15(2):A66

Rooney B. Racism, poverty, abortion, and other reproductive outcomes. Epidemiology. 2000; 11 (6):740-2

Stirling SS, Woolf L, North WR, Seghatchian MJ, Meade TW. Homeostasis in normal pregnancy, Throwb Haemost. 1984; 52(2):176-82

Dulícek P, Chrobák L, Kalousek l. Pesavová L. Pecka M, Stránsk9 P. Is factor V Leiden a risk factor for fetal loss? Acta Med. 1999; 42(3):93-6

Koster T, Rosendal FR, Ronde HD. Briet E. Vandenbroucke JP, Bertina RM. Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study. Lancet. 1993; 342(8886-8887): 1 503-6.

Published

2005-02-28

How to Cite

Zaccaria, R., Couto, E., Barini, R., Annicchino-Bizzacchi, J. M., Silva, J. C. G. da, & Silva, J. L. P. e. (2005). LEIDEN FACTOR V AND G2021 OA IN RECURRENT SPONTANEOUS ABORTION AND STILLBIRTH. Revista De Ciências Médicas, 14(1). Retrieved from https://periodicos.puc-campinas.edu.br/cienciasmedicas/article/view/1190

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