scholarly journals Association of VEGFA, factor V and prothrombin gene polymorphisms with early pregnancy loss

2021 ◽  
Vol 7 (2) ◽  
Author(s):  
Abdulbary A.M. Ahmed ◽  
◽  
Madina M. Azova ◽  
2015 ◽  
Vol 5 (5) ◽  
pp. 500-506
Author(s):  
E. V. Mashkina ◽  
K. A. Kovalenko ◽  
N. V. Fomina ◽  
T. P. Shkurat

2020 ◽  
Vol 56 (3) ◽  
pp. 379-382
Author(s):  
A. A. M. Ahmed ◽  
M. M. Azova ◽  
F. U. Ramazanova ◽  
O. B. Gigani

2005 ◽  
Vol 274 (2) ◽  
pp. 119-124 ◽  
Author(s):  
Venkata Suryanarayana ◽  
Lakshmi Rao ◽  
Murthy Kanakavalli ◽  
Venkata Padmalatha ◽  
Mamata Deenadayal ◽  
...  

2019 ◽  
Vol 23 (4) ◽  
pp. 381-389
Author(s):  
A. A. M. Ahmed ◽  
A. A. Muradian ◽  
M. M. Azova

Background. A variety of biological processes regulated by differential gene expression are required to maintain a normal gestation and accordingly, the mutations and polymorphisms in such genes may cause miscellaneous biological disorders that eventually result in early pregnancy loss. Many studies reported that aberrant fetal DNA methylation as well as embryonic chromosome abnormalities may lead to impairment of fetal early growth and development. Therefore, we have aimed to genotype several gene polymorphisms might be involved in the above-mentioned biological disorders to screen their prevalence in Russian population. Materials and methods. 81 Russian women without previous history of normal pregnancy or early abortion were recruited into this population study to determine the genotype and allele frequencies through genotyping using RFLP-PCR method for DNMT3B rs2424913, DNMT3B rs1569686, DNMT3A rs7590760, DNMT1 rs2228611, DNMT1 rs8101626, DNMT3L rs2276248, and DNMT3L rs2070565, allele-specific PCR for SYCP3 T657C, and real-time PCR for MTHFR rs1801133, MTHFR rs1801131, MTR rs1805087, and MTRR rs1801394. Results. Minor homozygous genotypes and minor alleles of the polymorphisms DNMT3B rs2424913 (TT: 11.1%, T: 37.05%), DNMT1 rs2228611 (GG: 18.5%, G: 40.75%), and DNMT1 rs8101626 (GG: 16.0%, G: 40.1%) were quite prevalent in Russian women and as frequent as those of the well-studied polymorphisms: MTRR rs1801394 (GG: 27.2%, G: 50.65%), MTHFR rs1801131 (CC: 17.3%, C: 40.15%), and MTHFR rs1801133 (TT: 11.1%, T: 29.0%).The heterozygous genotype of SYCP3 T657C (CT: 12.3%, T: 6.15%) was also quite frequent. Conclusion. Based on our study and literature data, we suggest that DNMT3B rs2424913, DNMT1 rs2228611, DNMT1 rs8101626, and SYCP3 T657C polymorphisms along with the common folate cycle gene polymorphisms can be potential genetic predictors for early pregnancy loss in Russian women.


2019 ◽  
Vol 167 (4) ◽  
pp. 475-478
Author(s):  
M. M. Azova ◽  
A. A. Ahmed ◽  
A. Ait Aissa ◽  
M. L. Blagonravov

2014 ◽  
Vol 12 (1) ◽  
pp. 19
Author(s):  
Yelena Vladimirovna Mashkina ◽  
Konstantin Alekseyevich Kovalenko ◽  
Nadezhda Vladimirovna Fomina ◽  
Tatyana Pavlovna Shkurat

2018 ◽  
Vol 6 (3) ◽  
pp. 85-88
Author(s):  
Shaima S. Mohammed ◽  
Rana A. Al-Timimy ◽  
Jinan N. Hassan ◽  
Najat T. Mahmood

Genetic causes of thrombophilia have been suggested as a possible cause of recurrent pregnancy loss (RPL). Fifty female patients aged between 21- 40 years and experienced at least two times early pregnancy loss were enrolled in the current study. Blood samples were aspirated, infectious (TORCH), hormonal (gonadotrophines, steroids, and thyroid hormones), ultrasonic, and serological (anti-lupus and anti-phospholipid antibodies) evaluations were conducted to exclude any individual candidate who had been suspected to have causes of early pregnancy loss rather than the genetic attribute. DNA from each particular sample was extracted by components of (FVL-PTH and MTHFR)StripAssay®A kit Vienna Lab Diagnostics GmbH, Vienna, Austria).this kit includes three steps: (1) DNA isolation, (2) Multiplex PCR amplification was performed by using biotinylated primers, for detecting different mutations in the three genes of interest (FVL-PTH and MTHFR) (3) Hybridization of amplification products to a test strip containing allele-specific oligonucleotide probes immobilized as an array of parallel lines. The results revealed that 24 samples out of 50 had MTHFR C677T mutations while 2 samples only had   FV (G1691A)mutation while prothrombin mutation (G20210A)has not been detected. In conclusion: genetic mutation had significant impact in patients suffered recurrent pregnancy loss.


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