Gene-gene interactions and prevalence of gene polymorphism associated with disorders of hemostasis and folate metabolism in patients with recurrent miscarriage
- Authors: Frolova N.I1, Belokrinitskaya T.E1, Strambovskaya N.N1, Belozertseva E.P1
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Affiliations:
- Chita State Medical Academy
- Issue: Vol 21, No 2 (2019)
- Pages: 18-22
- Section: Articles
- URL: https://ogarev-online.ru/2079-5831/article/view/33460
- DOI: https://doi.org/10.26442/20795696.2019.2.190345
- ID: 33460
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##article.viewOnOriginalSite##About the authors
Nataly I Frolova
Chita State Medical Academy
Email: *taasyaa@mail.ru
Cand. Sci. (Med.) Chita, Russia
Tatiana E Belokrinitskaya
Chita State Medical Academy
Email: tanbell24@mail.ru
D. Sci. (Med.), Full Prof. Chita, Russia
Nataliya N Strambovskaya
Chita State Medical Academy
Email: strambovskaya@yandex.ru
Cand. Sci. (Med.) Chita, Russia
Evgeniya P Belozertseva
Chita State Medical Academy
Email: belev.chita@mail.ru
Cand. Sci. (Med.) Chita, Russia
References
- Адамян Л.В., Артымук Н.В., Белокриницкая Т.Е. и др. Выкидыш в ранние сроки беременности: диагностика и тактика ведения. Клинические рекомендации (протокол) утв. Минздравом России 07.06.2016 №15-4/10/2-2482. М., 2016.
- Recurrent Pregnancy loss. ESHRE Guidline, November 2017.
- Kaiser J, Branch D.W. Recurrent Pregnancy Loss: Generally Accepted Causes and Their Management. Clin Obstet Gynecol 2016; 59 (3): 464-73. doi: 10.1097/GRF.0000000000000214
- Garrido-Gimenez C, Alijotas-Reig J. Recurrent miscarriage: causes, evaluation and management. Postgrad Med J 2015; 91 (1073): 51-62. doi: 10.1136/postgradmedj-2014-132672
- Sergi C, Al Jishi T, Walker M. Factor V Leiden mutation in women with early recurrent pregnancy loss: a meta-analysis and systematic review of the causal association. Arch Gynecol Obstet 2015; 291 (3): 671-9. doi: 10.1007/s00404-014-3443-x
- Farahmand K, Totonchi M, Hashemi M et al. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss. J Matern Fetal Neonatal Med 2016; 29 (8): 1269-73. doi: 10.3109/14767058.2015.1044431
- Kamali M, Hantoushzadeh S, Borna S et al. Association between Thrombophilic Genes Polymorphisms and Recurrent Pregnancy Loss Susceptibility in the Iranian Population: a Systematic Review and Meta-Analysis. Iran Biomed J 2018; 22 (2): 78-89.
- Al-Achkar W, Wafa A, Ammar S et al. Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women. Reprod Sci 2017; 24 (9): 1275-9. doi: 10.1177/1933719116682874
- Chen H, Yang X, Lu M. Methylenetetrahydrofolate reductase gene polymorphisms and recurrent pregnancy loss in China: a systematic review and meta-analysis. Arch Gynecol Obstet 2016; 293 (2): 283-90. doi: 10.1007/s00404-015-3894-8
- Yang Y, Luo Y, Yuan J et al. Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation. Arch Gynecol Obstet 2016; 293 (6): 1197-211. doi: 10.1007/s00404-015-3944-2
- Jeon Y.J, Kim Y.R, Lee B.E et al. Genetic association of five plasminogen activator inhibitor-1 (PAI-1) polymorphisms and idiopathic recurrent pregnancy loss in Korean women. Thromb Haemost 2013; 110 (4): 742-50.
- Chen H, Nie S, Lu M. Association between plasminogen activator inhibitor-1 gene polymorphisms and recurrent pregnancy loss: a systematic review and meta-analysis. Am J Reprod Immunol 2015; 73 (4): 292-300. doi: 10.1111/aji.12321
- Salazar Garcia MD, Sung N, Mullenix T.M et al. Plasminogen Activator Inhibitor-1 4G/5G Polymorphism is Associated with Reproductive Failure: Metabolic, Hormonal, and Immune Profiles. Am J Reprod Immunol 2016; 76 (1): 70-81. doi: 10.1111/aji.12516
- Guan L.X, Du X.Y, Wang J.X et al. Association of genetic polymorphisms in plasminogen activator inhibitor-1 gene and 5,10-methylenetetrahydrofolate reductase gene with recurrent early spontaneous abortion. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2005; 22 (3): 330-3.
- Parveen F, Tuteja M, Agrawal S. Polymorphisms in MTHFR, MTHFD, and PAI-1 and recurrent miscarriage among North Indian women. Arch Gynecol Obstet 2013; 288 (5): 1171-7.
- Li X, Liu Y, Zhang R et al. Meta-analysis of the association between plasminogen activator inhibitor-1 4G/5G polymorphism and recurrent pregnancy loss. Med Sci Monit 2015; 1051-6. doi: 10.12659/MSM.892898
- Moore J.H, Gilbert J.C, Tsai C.T et al. A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility. J Theoretic Biol 2006; 241: 252-61.
- Баранов В.С. Генетический паспорт - основа индивидуальной и предикативной медицины. СПб.: Н-Л, 2009. [Baranov V.S. Geneticheskii pasport - osnova individual'noi i predikativnoi meditsiny. Saint Petersburg: N-L, 2009 (in Russian).]
- Фролова Н.И., Белокриницкая Т.Е., Страмбовская Н.Н. Молекулярно-генетические предикторы осложнений беременности у молодых здоровых женщин. Дальневосточный мед. журн. 2015; 3: 29-30.
- Djurovic J, Stojkovic O, Todorovic J et al. Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations. Hum Fertil (Camb) 2017; 20 (2): 132-9. doi: 10.1080/14647273.2016.1255785
- Gonçalves R.O, Fraga L.R, Santos W.V et al. Association between the thrombophilic polymorphisms MTHFR C677T, Factor V Leiden, and prothrombin G20210A and recurrent miscarriage in Brazilian women. Genet Mol Res 2016; 15 (3). doi: 10.4238/gmr.15038156
- Cao Y, Xu J, Zhang Z et al. Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis. Gene 2013; 514 (2): 105-11. doi: 10.1016/j.gene.2012.10.091
- Nowak I, Bylińska A, Wilczyńska K et al. The methylenetetrahydrofolate reductase c.c.677 C>T and c.c.1298 A>C polymorphisms in reproductive failures: Experience from an RSA and RIF study on a Polish population. PLoS One 2017; 12 (10): e0186022. doi: 10.1371/journal.pone.0186022. eCollection 2017
- Момот А.П. Проблема тромбофилии в клинической практике. Рос. журн. детской гематологии и онкологии. 2015; 1: 36-48.
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