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Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis

It has been reported that oxidative and nitrative stress might be the pathogenesis of endometriosis. This prospective case-control study attempted to check the connection between single nucleotide polymorphism (SNP) of three antioxidant enzymes (glutathione peroxidase 4 (GPX4), thioredoxin 2 (TXN2),...

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Autores principales: Huang, Yun-Yao, Wu, Cheng-Hsuan, Liu, Chung-Hsien, Yang, Shun-Fa, Wang, Po-Hui, Lin, Long-Yao, Lee, Tsung-Hsien, Lee, Maw-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400372/
https://www.ncbi.nlm.nih.gov/pubmed/32679649
http://dx.doi.org/10.3390/ijerph17145089
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author Huang, Yun-Yao
Wu, Cheng-Hsuan
Liu, Chung-Hsien
Yang, Shun-Fa
Wang, Po-Hui
Lin, Long-Yao
Lee, Tsung-Hsien
Lee, Maw-Sheng
author_facet Huang, Yun-Yao
Wu, Cheng-Hsuan
Liu, Chung-Hsien
Yang, Shun-Fa
Wang, Po-Hui
Lin, Long-Yao
Lee, Tsung-Hsien
Lee, Maw-Sheng
author_sort Huang, Yun-Yao
collection PubMed
description It has been reported that oxidative and nitrative stress might be the pathogenesis of endometriosis. This prospective case-control study attempted to check the connection between single nucleotide polymorphism (SNP) of three antioxidant enzymes (glutathione peroxidase 4 (GPX4), thioredoxin 2 (TXN2), thioredoxin reductase 1 (TXNRD1)) and endometriosis. We recruited 90 patients with histology-approved endometriosis as the case group and 130 age-matched women for an annual pap smear examination as the control group. The stage of endometriosis was evaluated with revised ASRM score. Both groups were genotyped in the peripheral leukocytes for the SNP of GPX4 (rs713041), TXN2 (rs4821494) and TXNRD1 (rs1128446) by PCR-based methods. An X(2) test was used to analysis of the difference of allele frequency and SNP distribution between two groups. The results revealed GPX4 (rs713041) has a significantly different distribution between two groups (C:T = 116 (44.6%):144 (55.4%) in control and C:T = 104 (57.8%): 76 (42.2%) in endometriosis groups, p = 0.007). The SNP in TXN2 (rs4821494) also showed a difference in allele frequency (G:T = 180 (69.2%):80 (30.8%) in control and G:T = 141 (78.3%):39 (21.6%) in endometriosis group, p = 0.030). In addition, the SNP GPX4 (rs713041) was associated with the severity of the endometriosis. Women who have advanced stage endometriosis were different from mild endometriosis in genetic variants of GPX4 gene (p = 0.001). In conclusion, the relationship between endometriosis and SNP of antioxidant enzymes, GPX4 and TXN2, was confirmed by the present study. According to the result, we suggested that the GPX4 might contribute to the pathogenesis of endometriosis.
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spelling pubmed-74003722020-08-23 Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis Huang, Yun-Yao Wu, Cheng-Hsuan Liu, Chung-Hsien Yang, Shun-Fa Wang, Po-Hui Lin, Long-Yao Lee, Tsung-Hsien Lee, Maw-Sheng Int J Environ Res Public Health Article It has been reported that oxidative and nitrative stress might be the pathogenesis of endometriosis. This prospective case-control study attempted to check the connection between single nucleotide polymorphism (SNP) of three antioxidant enzymes (glutathione peroxidase 4 (GPX4), thioredoxin 2 (TXN2), thioredoxin reductase 1 (TXNRD1)) and endometriosis. We recruited 90 patients with histology-approved endometriosis as the case group and 130 age-matched women for an annual pap smear examination as the control group. The stage of endometriosis was evaluated with revised ASRM score. Both groups were genotyped in the peripheral leukocytes for the SNP of GPX4 (rs713041), TXN2 (rs4821494) and TXNRD1 (rs1128446) by PCR-based methods. An X(2) test was used to analysis of the difference of allele frequency and SNP distribution between two groups. The results revealed GPX4 (rs713041) has a significantly different distribution between two groups (C:T = 116 (44.6%):144 (55.4%) in control and C:T = 104 (57.8%): 76 (42.2%) in endometriosis groups, p = 0.007). The SNP in TXN2 (rs4821494) also showed a difference in allele frequency (G:T = 180 (69.2%):80 (30.8%) in control and G:T = 141 (78.3%):39 (21.6%) in endometriosis group, p = 0.030). In addition, the SNP GPX4 (rs713041) was associated with the severity of the endometriosis. Women who have advanced stage endometriosis were different from mild endometriosis in genetic variants of GPX4 gene (p = 0.001). In conclusion, the relationship between endometriosis and SNP of antioxidant enzymes, GPX4 and TXN2, was confirmed by the present study. According to the result, we suggested that the GPX4 might contribute to the pathogenesis of endometriosis. MDPI 2020-07-15 2020-07 /pmc/articles/PMC7400372/ /pubmed/32679649 http://dx.doi.org/10.3390/ijerph17145089 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huang, Yun-Yao
Wu, Cheng-Hsuan
Liu, Chung-Hsien
Yang, Shun-Fa
Wang, Po-Hui
Lin, Long-Yao
Lee, Tsung-Hsien
Lee, Maw-Sheng
Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title_full Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title_fullStr Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title_full_unstemmed Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title_short Association between the Genetic Variants of Glutathione Peroxidase 4 and Severity of Endometriosis
title_sort association between the genetic variants of glutathione peroxidase 4 and severity of endometriosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400372/
https://www.ncbi.nlm.nih.gov/pubmed/32679649
http://dx.doi.org/10.3390/ijerph17145089
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