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No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran

Background: Endometriosis is one of the most common gynecologic disorders. It is a complex trait and both genetic and environmental factors have been implicated in its pathogenesis. There is growing evidence indicating that exposure to environmental contaminants is a risk factor for endometriosis. G...

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Autores principales: Seifati, Seyed Morteza, Parivar, Kazem, Aflatoonian, Abbas, Dehghani Firouzabadi, Razieh, Sheikhha, Mohammad Hasan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163259/
https://www.ncbi.nlm.nih.gov/pubmed/25242970
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author Seifati, Seyed Morteza
Parivar, Kazem
Aflatoonian, Abbas
Dehghani Firouzabadi, Razieh
Sheikhha, Mohammad Hasan
author_facet Seifati, Seyed Morteza
Parivar, Kazem
Aflatoonian, Abbas
Dehghani Firouzabadi, Razieh
Sheikhha, Mohammad Hasan
author_sort Seifati, Seyed Morteza
collection PubMed
description Background: Endometriosis is one of the most common gynecologic disorders. It is a complex trait and both genetic and environmental factors have been implicated in its pathogenesis. There is growing evidence indicating that exposure to environmental contaminants is a risk factor for endometriosis. Glutathione-S-Transferase M1 (GSTM1) is one of the genes involved in detoxification of endogenous and exogenous compounds. Objective: Several studies have indicated an association between GSTM1 null mutation and endometriosis. In this study, the possible association between the GSTM1 gene null genotype and susceptibility to endometriosis in woman from central and southern Iran was investigated. Materials and Methods: One hundred and one unrelated premenopausal women with endometriosis and 142 unrelated healthy premenopausal women without endometriosis were enrolled in the study. Genomic DNA was extracted from Peripheral blood in all subjects. GSTM1 null genotyping was performed by polymerase chain reaction (PCR). Results: There was no significant difference between frequencies of GSTM1 null genotype in case and control groups (50.5% Vs. 52.1%, p=0.804). Furthermore, this genotype was not associated with severity of endometriosis in our sample (p=0.77). Conclusion : further studies involving gene-environment and gene-gene interactions, particularly combination of GSTM1 and other GST gene family polymorphisms are needed.
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spelling pubmed-41632592014-09-19 No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran Seifati, Seyed Morteza Parivar, Kazem Aflatoonian, Abbas Dehghani Firouzabadi, Razieh Sheikhha, Mohammad Hasan Iran J Reprod Med Original Article Background: Endometriosis is one of the most common gynecologic disorders. It is a complex trait and both genetic and environmental factors have been implicated in its pathogenesis. There is growing evidence indicating that exposure to environmental contaminants is a risk factor for endometriosis. Glutathione-S-Transferase M1 (GSTM1) is one of the genes involved in detoxification of endogenous and exogenous compounds. Objective: Several studies have indicated an association between GSTM1 null mutation and endometriosis. In this study, the possible association between the GSTM1 gene null genotype and susceptibility to endometriosis in woman from central and southern Iran was investigated. Materials and Methods: One hundred and one unrelated premenopausal women with endometriosis and 142 unrelated healthy premenopausal women without endometriosis were enrolled in the study. Genomic DNA was extracted from Peripheral blood in all subjects. GSTM1 null genotyping was performed by polymerase chain reaction (PCR). Results: There was no significant difference between frequencies of GSTM1 null genotype in case and control groups (50.5% Vs. 52.1%, p=0.804). Furthermore, this genotype was not associated with severity of endometriosis in our sample (p=0.77). Conclusion : further studies involving gene-environment and gene-gene interactions, particularly combination of GSTM1 and other GST gene family polymorphisms are needed. Research and Clinical Center for Infertility 2012-01 /pmc/articles/PMC4163259/ /pubmed/25242970 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Seifati, Seyed Morteza
Parivar, Kazem
Aflatoonian, Abbas
Dehghani Firouzabadi, Razieh
Sheikhha, Mohammad Hasan
No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title_full No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title_fullStr No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title_full_unstemmed No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title_short No association of GSTM1 null polymorphism with endometriosis in women from central and southern Iran
title_sort no association of gstm1 null polymorphism with endometriosis in women from central and southern iran
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163259/
https://www.ncbi.nlm.nih.gov/pubmed/25242970
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