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

Bibliographic Data

ID15467744
AuthorsYun-Yao Huang (Chung Shan Medical University Hospital), Cheng-Hsuan Wu (0000-0002-3610-5993, Kaohsiung Medical University), Chung-Hsien Liu (0000-0002-2938-8454, Chung Shan Medical University Hospital), Shun‐Fa Yang (0000-0002-0365-7927, Chung Shan Medical University Hospital), Po-Hui Wang (Chung Shan Medical University Hospital), Long-Yao Lin (Chung Shan Medical University Hospital), Tsung‐Hsien Lee (0000-0001-8858-0916, Chung Shan Medical University Hospital, corresponding author), Maw‐Sheng Lee (0000-0001-6234-5432, Chung Shan Medical University Hospital), Maw-Sheng Lee (Department of Obstetrics and Gynecology, Chung Shan Medical University Hospital, Taichung 40203, Taiwan)
Year2020
Volume17
Issue14
Pages5089-5089
Publication date2020-07-15
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph17145089
PMID32679649
OpenAlexW3043021456
LanguageEN
References cited24

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

Allele · Allele frequency · Biology · Endometriosis · Gene · Genotype · Glutathione peroxidase · GPX4 · Oxidative stress · Single-nucleotide polymorphism · SNP · Endometriosis Research and Treatment · Genomics, phytochemicals, and oxidative stress · Glutathione Transferases and Polymorphisms · Medicine · Gastroenterology · Genetics · Internal Medicine

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