Literature DB >> 20728041

Endothelial nitric oxide synthase gene polymorphisms (-786T>C, 4a4b, 894G>T) and haplotypes in Korean patients with recurrent spontaneous abortion.

Seung Ju Shin1, Hyun Haing Lee, Sun Hee Cha, Ji Hyang Kim, Sung Han Shim, Dong Hee Choi, Nam Keun Kim.   

Abstract

OBJECTIVE: To investigate the association of three common polymorphisms (-786T>C, 4a4b, 894G>T) of the endothelial nitric oxide synthase (eNOS) gene with idiopathic recurrent spontaneous abortion (RSA). STUDY
DESIGN: In a prospective case-control study, 340 patients with unexplained recurrent spontaneous abortion and 115 controls with at least one live birth and no history of pregnancy loss were enrolled. Polymerase chain reaction and restriction fragment length polymorphism analysis were performed to identify the genotypes.
RESULTS: The recurrent spontaneous abortion patients exhibited a significantly higher frequency of the eNOS 894GT+TT genotype (Odds ratio (OR), 2.39; 95% confidence interval (CI), 1.25-4.58; p=0.008) compared to the control group; no significant differences in the -786T>C and 4a4b genotype frequencies were observed. The eNOS 894GT genotype (OR, 1.94; 95% CI, 1.00-3.75; p=0.056) was marginally different between recurrent spontaneous abortion and control groups. The frequency of the -786T-4b-894T haplotype (p=0.001) was significantly higher in the idiopathic RSA group than in the control group.
CONCLUSION: The eNOS 894GT+TT genotype and the -786T-4b-894T haplotype are significantly associated with idiopathic recurrent spontaneous abortion in Korean women. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20728041     DOI: 10.1016/j.ejogrb.2010.05.014

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  5 in total

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Journal:  Mol Biol Rep       Date:  2014-02-23       Impact factor: 2.316

2.  The incidence of NOS3 gene polymorphisms on newborns with large and small birth weight.

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3.  The interaction effect of angiogenesis and endothelial dysfunction-related gene variants increases the susceptibility of recurrent pregnancy loss.

Authors:  E A Trifonova; M G Swarovskaya; O A Ganzha; O V Voronkova; T V Gabidulina; V A Stepanov
Journal:  J Assist Reprod Genet       Date:  2019-01-24       Impact factor: 3.412

Review 4.  Genetics of recurrent pregnancy loss among Iranian population.

Authors:  Meysam Moghbeli
Journal:  Mol Genet Genomic Med       Date:  2019-07-30       Impact factor: 2.183

5.  Methylenetetrahydrofolate Reductase C677T and A1298C Mutations in Women with Recurrent Spontaneous Abortions in the Northwest of Iran.

Authors:  Ahmad Poursadegh Zonouzi; Nader Chaparzadeh; Mehrdad Asghari Estiar; Mahzad Mehrzad Sadaghiani; Laya Farzadi; Alieh Ghasemzadeh; Masoud Sakhinia; Ebrahim Sakhinia
Journal:  ISRN Obstet Gynecol       Date:  2012-11-14
  5 in total

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