Preview

Medical Genetics

Advanced search

STUDY OF THE ROLE OF POLYMORPHISM OF GENE OF HAEMOSTASIS SYSTEM IN OCCURRENCE OF PRETERM BIRTH AMONG WOMEN OF UZBEK POPULATION

https://doi.org/10.1234/XXXX-XXXX-2015-5-37-41

Abstract

There has been performed analysis of the presence of mutagenic allele «1691А» gene FV Leiden and C677T gene MTGFR among the women with preterm labor. The carriers of mutant allele «1691А» in the hetero- or homozygous state among the women with preterm labors accounted for 8,5% that corresponded to 4,5 fold increase of the risk factor for development of venous thrombosis in comparison with control group (OR = 4.64; 95% CI 0.98—22.02). Differences in the frequency of prevalence of heterozygous variant of polymorphism C677T gene MTGFR between general groups of women with preterm labor and controls had statistic unreliable character. However, the carrying of the homozygous allele of this marker defined more than 4-fold increase in risk of the development of the venous thrombosis in comparison with control group (OR = 4.08: 95%CI 0,05—19,7), that indicated about participation of this marker in the development of venous thrombosis.

 

About the Authors

N. I. Lubchich
Republican specialized scientific-practice medical center of obstetrics and gynecology, Tashkent
Uzbekistan

100124 Mirzo Ulugbek street 132a



K. T. Boboev
Scientific-research institute of hematology and hemotransfusiology
Uzbekistan
100059, Usman Nasir street 138, Tashkent


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 учёной 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 al. 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.


Review

For citations:


Lubchich N.I., Boboev K.T. STUDY OF THE ROLE OF POLYMORPHISM OF GENE OF HAEMOSTASIS SYSTEM IN OCCURRENCE OF PRETERM BIRTH AMONG WOMEN OF UZBEK POPULATION. Medical Genetics. 2015;14(5):37-41. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2015-5-37-41

Views: 651


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2073-7998 (Print)