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Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion

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Abstract

Factor V Leiden (FVL) G1691A, methylenetetrahydrofolate reductase (MTHFR) C677T, and factor II (FII) G20210A mutations are three important causes of thrombophilia, the condition that might be related to infertility and recurrent spontaneous abortion (RSA). In this study we evaluated the presence of these three mutations in 36 female patients with unexplained infertility, 65 female patients with unexplained RSA, and 62 healthy fertile women as control group. DNA was extracted from peripheral blood samples and PCR-RFLP was performed for the molecular diagnosis of each mutation. In addition, activated protein C resistance (APC-R) was also evaluated. The frequencies of FVL, MTHFR, and FII mutations (heterozygous and homozygous) in the control group were 0.0%, 38.7%, and 3.2%, respectively. The frequency of FVL mutation in patients with infertility (30.6%) or RSA (20.0%) was significantly higher than that of the control group. A significantly higher MTHFR mutation rate was also observed in patients with RSA (63.1%) as compared to controls. However, the mutation rate of MTHFR in patients with infertility (50.0%) was not statistically different from that in controls. No significant difference was observed in the frequencies of FII mutations between the patients and controls. Decreased levels of APC-R were observed in 25.0% of infertile patients and 18.9% of patients with RSA. In conclusion, our results show a skew towards higher mutation frequencies of FVL and MTHFR in patients that may necessitate detection of such mutations in these Iranian patients.

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References

  1. Kovalevsky G, Gracia CR, Berlin JA, Sammel MD, Barnhart KT (2004) Evaluation of the association between hereditary thrombophilias and recurrent pregnancy loss: a meta-analysis. Arch Intern Med 164(5):558−563

    Article  PubMed  Google Scholar 

  2. Lane DA, Mannucci PM, Bauer KA, Bertina RM, Bochkov NP, Boulyjenkov V et al (1996) Inherited thrombophilia: part 1. Thromb Haemost 76:651−662

    PubMed  CAS  Google Scholar 

  3. Lane DA, Mannucci PM, Bauer KA, Bertina RM, Bochkov NP, Boulyjenkov V et al (1996) Inherited thrombophilia: part 2. Thromb Haemost 76:824−834

    PubMed  CAS  Google Scholar 

  4. De Stefano V, Finazzi G, Mannucci PM. (1996) Inherited thrombophilia: pathogenesis, clinical syndromes, and management. Blood 87:3531−3544

    PubMed  CAS  Google Scholar 

  5. Vefring H, Lie RT, ODegard R, Mansoor MA, Nilsen ST (2004) Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia. Epidemiology 15(3):317−322

    Article  PubMed  Google Scholar 

  6. Wisotzkey JD, Bayliss P, Rutherford E, Bell T (1999) Placental genotyping of the factor V Leiden, prothrombin 20210A and the methylenetetrahydrofolate reductase (MTHFR) C677T alleles in IUGR pregnancies. Thromb Haemost 81(5):844−845

    PubMed  CAS  Google Scholar 

  7. Zoller B, Svensson PJ, He X, Dahlback B (1994) Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. J Clin Invest 94:2521−2524

    Article  PubMed  CAS  Google Scholar 

  8. Major DA, Sane DC, Herrington DM (2000) Cardiovascular implications of the factor V Leiden mutation. Am Heart J 140(2):189−195

    Article  PubMed  CAS  Google Scholar 

  9. Candito M, Magnaldo S, Bayle J, Dor JF, Gillet Y, Bongain A et al (2003) Clinical B12 deficiency in one case of recurrent spontaneous pregnancy loss. Clin Chem Lab 41(8):1026−1027

    Article  CAS  Google Scholar 

  10. Poort SR, Rosendaal FR, Reitsma PH, Bertina RM (1996) A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 88:3698−3703

    PubMed  CAS  Google Scholar 

  11. Prandoni P, Lensing AWA, Cogo A, Cuppini S, Villalta S, Carta M et al (1996) The long-term clinical course of acute deep venous thrombosis. Ann Intern Med 125:1−7

    PubMed  CAS  Google Scholar 

  12. Van den Belt AGM, Sanson BJ, Simioni P, Prandoni P, Buller HR, Girolami A et al (1997) Recurrence of venous thromboembolism in patients with familial thrombophilia. Arch Intern Med 157:2227−2232

    Article  PubMed  CAS  Google Scholar 

  13. Sarig G, Younis JS, Hoffman R, Lanir N, Blumenfeld Z, Brenner B (2002) Thrombophilia is common in women with idiopathic pregnancy loss and is associated with late pregnancy wastage. Fertil Steril 77(2):342−347

    Article  PubMed  Google Scholar 

  14. Finan RR, Tamim H, Ameen G, Sharida HE, Rashid M, Almawi WY (2002) Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population. Am J Hematol 71(4):300−305

    Article  PubMed  CAS  Google Scholar 

  15. Rand JH, Luong TH (1999) Thrombophilias: diagnosis and treatment of thrombophilia relating to contraception and pregnancy. Semin Hematol 36:2−9

    PubMed  CAS  Google Scholar 

  16. Rosendaal FR (1999) Venous thrombosis: a multicausal disease. Lancet 353:1167−1173

    Article  PubMed  CAS  Google Scholar 

  17. Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG et al (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10(1):111−113

    Article  PubMed  CAS  Google Scholar 

  18. Morita H, Kurihara H, Tsubaki S, Sugiyama T, Hamada C, Kurihara Y et al (1998) Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese. Arterioscler Thromb Vasc Biol 18(9):1465−1469

    PubMed  CAS  Google Scholar 

  19. Adjalla CE, Amouzou EK, Sanni A, Abdelmouttaleb I, Chabi NW, Namour F et al (2003) Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populations. Clin Chem Lab Med 41(8):1028−1032

    Article  PubMed  CAS  Google Scholar 

  20. Rousseau F, Rehel R, Rouillard P, DeGranpre P, Khandjian EW (1994) High throughput and economical mutation detection and RFLP analysis using a minimethod for DNA preparation from whole blood and acrylamide gel electrophoresis. Hum Mutat 4(1):51−54

    Article  PubMed  CAS  Google Scholar 

  21. Pauler HU, Voigt-Tschirschwitz T, Hinney B, Burfeind P, Wolf C, Emons G (2003) Analyzes of three common thrombophilic gene mutations in German women with recurrent abortions. Acta Obstet Gynecol Scand 82:942−947

    Article  PubMed  Google Scholar 

  22. Zeinali S, Duca F, Zarbakhsh B, Tagliabue L, Mannucci PM (2000) Thrombophilic mutations in Iran. Thromb Haemost 83(2):351−352

    PubMed  CAS  Google Scholar 

  23. Souza SS, Ferriani RA, Pontes AG, Zago MA, Franco RF (1999) Factor V leiden and factor II G20210A mutations in patients with recurrent abortion. Hum Reprod 14(10):2448−2450

    Article  PubMed  CAS  Google Scholar 

  24. Glueck CJ, Wang P, Goldenberg N, Sieve L (2004) Pregnancy loss, polycystic ovary syndrome, thrombophilia, hypofibrinolysis, enoxaparin, metformin. Clin Appl Thromb Hemost 10(4):323−334

    Article  PubMed  CAS  Google Scholar 

  25. Hashimoto K, Shizusawa Y, Shimoya K, Ohashi K, Shimizu T, Azuma C et al (1999) The factor V Leiden mutation in Japanese couples with recurrent spontaneous abortion. Hum Reprod 14(7):1872−1874

    Article  PubMed  CAS  Google Scholar 

  26. Golbahar J, Hamidi A, Aminzadeh MA, Omrani GR (2004) Association of plasma folate, plasma total homocysteine, but not methylenetetrahydrofolate reductase C667T polymorphism, with bone mineral density in postmenopausal Iranian women: a cross-sectional study. Bone 35(3):760−765

    Article  PubMed  CAS  Google Scholar 

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Acknowledgement

We would like to express our sincerest appreciation to Dr. Akhondi as the chairman of Avesina Research Institute for his kindness in providing all of the expenses of this project.

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Correspondence to Mohammad Hossein Modarressi.

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Behjati, R., Modarressi, M.H., Jeddi-Tehrani, M. et al. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion. Ann Hematol 85, 268–271 (2006). https://doi.org/10.1007/s00277-005-0021-0

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  • DOI: https://doi.org/10.1007/s00277-005-0021-0

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