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Analysis of C667T polymorphism of MTHFR gene in women with preterm labor

https://doi.org/10.1234/XXXX-XXXX-2015-11-36-39

Abstract

An analysis of the presence of C677T mutant allele of MTHFR gene among the women with preterm labor was performed. The difference in the frequency of heterozygous C677T polymorphism in the MTHFR locus between the general groups of women with preterm labor and the controls was statistically unreliable. However, the carrier state of the homozygous mutant allele T in this locus determined increased risk of early and very early preterm labor in comparison with the control group (OR = 2.3; 95%CI 1.22-3.32). This finding indicates that this genetic marker is involved in the progression of venous thrombosis.

About the Authors

N. I. Lubchich
Republican specialized scientific-practice medical center of obstetrics and gynecology
Russian Federation


K. T. Boboev
Scientific-research institute of hematology and hemotransfusiology
Russian Federation


References

1. Баранов В.С. Генетический паспорт - основа индивидуальной и предиктивной медицины. - СПб.: Изд-во научной лит-ры, 2009. - 527 с.

2. Блинецкая С.Л. Основные наследственные тромбофилии и их роль при привычном невынашивании беременности: Автореф. дисс. на соискание ученой степени к.м.н. - М., 2009. - 21 с.

3. Канева Ф.М., Ахметова В.Г., Фролов А.Л. и др. Анализ мутаций G20210A гена PRТ, G1691А гена FV и С677Т гена MTHFR у женщин с невынашиванием беременности // Клин. лаб. диагностика. - 2006. - №9. - С. 45.

4. Макацария А.Д., Пшеничникова Е.Б., Пшеничникова Г.Б. и др. Метаболический синдром и тромбофилия в акушерстве и гинекологии. - М.: Мед. информ. агентство, 2006. - №1. - С. 44-46.

5. Репина М.Ф., Сумская Г.Ф., Лапина Е.М. и др. Особенности течения беременности у женщин с наследственными формами тромбофилии // Журн. акуш. и жен. бол. - 2007. - T. LV1. - Вып. 2. - С. 3-9.

6. Решетняк T.M. Тромбофилии, тромбозы и беременность // Проблемы гемостазиологии в акушерстве и гинекологии // Человек и лекарство: Тез. докл 13-го Рос. нац. конгресса. - М., 2006. - С. 4-16.

7. Baglin T., Gray E., Greaves M. Clinical guidelines for testing for heritable thrombophilia // Brit. J. Haematol. - 2010. - Vol. 149. - P. 209-220.

8. Botto N., Maffei S., Manfredi S. et al. Prothrombotic mutations, family history and the risk of thrombosis in postmenopausal women: implications for hormone replacement therapy // Climacteric. - 2011. - Vol. 13, №6. - P. 25-30.

9. Folkeringa N., Brouwer J.L., Korteweg F.J. et al. High risk of pregnancy-related venous thromboembolism in women with multiple thrombophilic defects // Brit. J. Haematol. - 2007. - Vol. 138, №1. - P. 110-116.

10. Khan S. Hereditary thrombophilia // Thromb. J. - 2006. - Vol. 4. - P. 234-236.

11. Kovac M., Mitic G., Mikovic Z. et al. Thrombophilia in Women with Pregnancy-Associated Complications: Fetal Loss and Pregnancy-Related Venous Thromboembolism // Gynec. Obstet. Invest. - 2010. - Vol. 69. - P. 233-238.

12. Kosar A., Kasapoglu B., Kalyoncu S. Et all. Treatment of adverse perinatal outcome in inherited thrombophilias: a clinical study // Blood Coagulation & Fibrinolysis. - 2011. - Vol. 22. - P. 14.18.

13. Rodger M.A., Paidas M., McLintock C. et al. Inherited thrombophilia and pregnancy complications revisited // Obstet. Gynec. - 2008. - Vol. 112. - P. 320-324.


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For citations:


Lubchich N.I., Boboev K.T. Analysis of C667T polymorphism of MTHFR gene in women with preterm labor. Medical Genetics. 2015;14(11):36-39. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2015-11-36-39

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