Abstract

BackgroundEndometrial hyperplasia (EH) occurs when the endometrium, the lining of the uterus, becomes too thick, causing abnormal uterine bleeding. In some cases, it can lead to endometrial carcinoma if untreated. Glutathione-S-transferases (GSTs) enzymes have a role in the metabolism of a lot of disease-causing carcinogens and mutagens that are present in environments of human. GSTP1–313 A>G gene polymorphism was associated with significantly high risk of endometrial carcinoma in some reports. The aim of this work is to assess the association of this polymorphism with the susceptibility of EH among a sample of Egyptian women. Subjects and methodsThis study included 84 unrelated EH Egyptian women who were compared to 134 healthy controls from the same locality. For all subjects, DNA was genotyped for GSTP1–313 A>G (Ile105Val) polymorphism using the PCR–RFLP technique. ResultsThe frequency of GSTP1–313 AG and GG genotypes was noted to be significantly higher among most of the cases with EH compared to controls (79.8% vs. 42.0%, OR=8.63, 95% CI=4.53–16.46, p<0.001). Also the frequency of the GSTP1–313 G allele was significantly higher among most of the cases compared to controls (24.9% vs. 16.8%, OR=3.72, 95% CI=2.39–5.79, p<0.001). Furthermore, there was a significant increase of endometrial thickness in the EH women compared to controls (p<0.001). ConclusionsGSTP1–313 G allele carriage was associated with susceptibility of EH among a sample of Egyptian women.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.