European Journal of Obstetrics & Gynecology and Reproductive Biology
Volume 139, Issue 1 , Pages 53-58, July 2008

The endothelial nitric oxide synthase Glu298Asp polymorphism is not a risk factor for endometriosis in south Indian women

  • Manjula Bhanoori

      Affiliations

    • Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500007, India1
  • ,
  • D.B. Kameshwari

      Affiliations

    • Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500007, India1
  • ,
  • K.T. Zondervan

      Affiliations

    • Wellcome Trust Centre for Human Genetics, University of Oxford, UK
  • ,
  • Mamata Deenadayal

      Affiliations

    • Infertility Institute and Research Centre, Hyderabad, India
  • ,
  • Stephen Kennedy

      Affiliations

    • Nuffield Department of Obstetrics & Gynaecology, University of Oxford, John Radcliffe Hospital, Oxford, UK
  • ,
  • S. Shivaji

      Affiliations

    • Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500007, India1
    • Corresponding Author InformationCorresponding author. Tel.: +91 40 27192504; fax: +91 40 27160591.

Received 12 July 2007; received in revised form 25 October 2007; accepted 13 January 2008. published online 04 March 2008.

Abstract 

Objective

To investigate whether the eNOS gene influences the risk of developing endometriosis in south Indian women.

Study design

The single nucleotide polymorphism, Glu298Asp, in exon7 of the eNOS gene was tested for association in a case–control study of 232 affected women and 210 women with no evidence of disease. All the women were infertile, ascertained from the same infertility clinic. The genotype frequencies of the polymorphism were compared, using polymerase chain reaction and sequencing analysis. The localization and expression of eNOS in the eutopic endometrium of five cases and four controls was also analyzed using immunohistochemistry and western blotting.

Results

No statistically significant differences were observed in the genotype distributions and allele frequencies (p=0.3) between the cases and controls according to codominant, dominant and recessive genotype models. The localization and expression of this protein were similar in the endometrium of cases and controls.

Conclusion

In the present study we could neither observe a difference in the eNOS expression nor establish an association between the eNOS Glu298Asp exon 7 polymorphism in south Indian women with endometriosis.

Keywords: Endometriosis, eNOS, Polymorphism

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PII: S0301-2115(08)00012-2

doi:10.1016/j.ejogrb.2008.01.006

European Journal of Obstetrics & Gynecology and Reproductive Biology
Volume 139, Issue 1 , Pages 53-58, July 2008