Mthfr c677t polymorphism in turkish women with polycystic ovary syndrome; [Polikistik over sendromlu türk kadınlarında mthfr c677t polimorfizmi]

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Özet

Objective: Polycystic ovary syndrome (PCOS) is one of the most common endocrine-reproductive-metabolic disorders of women at reproductive age, affecting 5-15% of the women worldwide. Although the pathogenesis of PCOS is not well defi-ned, it is associated with an increased risk of premature coronary artery disease (CAD). Hyperhomocysteinemia (HHcy) is associated with hyperlipidemia and is an independent risk factor for CAD. The most common cause of HHcy is related to the deficiency of methylenetetrahydrofolate reductase (MTHFR). This study aimed to investigate the relationship between different genotypes of MTHFR C677T and the risk of PCOS. Material and Methods: Two hundred twenty voluntary premenopausal women (110 healthy controls and 110 PCOS patients) were in-cluded in the study. All the volunteers underwent a physical examination along with biochemical hormonal evaluation and genetic analysis. Results: The genotyping analyses and genetic model of inheritance analyses revealed that the frequencies of CC, CT, and TT genotypes in the control and PCOS group to be 51.8%, 45.5%, and 2.7% and 51.8%, 48.2%, and 0%, respectively. The frequency of C and T alleles in the control and PCOS group was determined to be 74% (C: 0.74/155) and 26% (T: 0.26/53), and 75% (C: 0.75/167) and 25% (T: 0.25/53), respectively. The “T” additive, “T” dominant, and “C” recessive models it found that the CT vs. CC (OR:1.06 Cl:0.62-1.83), CC vs. TC+TT (OR: 0.99 Cl: 0.58-1.72), and TC+TT vs. CC (OR: 0.99 Cl: 0.58-1.70), respectively, did not show an increase in the PCOS risk. Conclusion: Our findings indicated that the different genotypes of MTHFR C677T were not associated with the risk of PCOS in Turkish women from Central Anatolia. © 2021 by Society of Endocrinology and Metabolism of Turkey.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13407Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.25179/tjem.2020-78794Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorPolat, Seher
dc.contributor.authorŞimşek, Yasin
dc.date.accessioned2026-10-18T20:28:14.589181747Z
dc.date.available2026-10-18T20:28:14.589181747Z
dc.date.issued2021
dc.description.abstractObjective: Polycystic ovary syndrome (PCOS) is one of the most common endocrine-reproductive-metabolic disorders of women at reproductive age, affecting 5-15% of the women worldwide. Although the pathogenesis of PCOS is not well defi-ned, it is associated with an increased risk of premature coronary artery disease (CAD). Hyperhomocysteinemia (HHcy) is associated with hyperlipidemia and is an independent risk factor for CAD. The most common cause of HHcy is related to the deficiency of methylenetetrahydrofolate reductase (MTHFR). This study aimed to investigate the relationship between different genotypes of MTHFR C677T and the risk of PCOS. Material and Methods: Two hundred twenty voluntary premenopausal women (110 healthy controls and 110 PCOS patients) were in-cluded in the study. All the volunteers underwent a physical examination along with biochemical hormonal evaluation and genetic analysis. Results: The genotyping analyses and genetic model of inheritance analyses revealed that the frequencies of CC, CT, and TT genotypes in the control and PCOS group to be 51.8%, 45.5%, and 2.7% and 51.8%, 48.2%, and 0%, respectively. The frequency of C and T alleles in the control and PCOS group was determined to be 74% (C: 0.74/155) and 26% (T: 0.26/53), and 75% (C: 0.75/167) and 25% (T: 0.25/53), respectively. The “T” additive, “T” dominant, and “C” recessive models it found that the CT vs. CC (OR:1.06 Cl:0.62-1.83), CC vs. TC+TT (OR: 0.99 Cl: 0.58-1.72), and TC+TT vs. CC (OR: 0.99 Cl: 0.58-1.70), respectively, did not show an increase in the PCOS risk. Conclusion: Our findings indicated that the different genotypes of MTHFR C677T were not associated with the risk of PCOS in Turkish women from Central Anatolia. © 2021 by Society of Endocrinology and Metabolism of Turkey.
dc.identifier.doi10.25179/tjem.2020-78794
dc.identifier.eissn1308-9846
dc.identifier.endpage112
dc.identifier.issn1301-2193
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85103020846
dc.identifier.startpage102
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13407
dc.identifier.volume25
dc.identifier.wosWOS:000627743000013
dc.language.isoen
dc.publisherTurkiye Klinikleri
dc.relation.ispartofTurkish Journal of Endocrinology and Metabolism
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMethylenetetrahydrofolate reductase gene
dc.subjectPolycystic ovary syndrome
dc.subjectPolymorphism, risk assessment
dc.subjectfollitropin
dc.subjectluteinizing hormone
dc.subjectmethylenetetrahydrofolate reductase (NADPH2)
dc.subjectprasterone sulfate
dc.subjecttestosterone
dc.subjectthyrotropin
dc.subjectacromegaly
dc.subjectadult
dc.subjectArticle
dc.subjectbody mass
dc.subjectcarbohydrate intolerance
dc.subjectchemiluminescence immunoassay
dc.subjectcontrolled study
dc.subjectcoronary artery disease
dc.subjectfemale
dc.subjectfolate metabolism
dc.subjectgene
dc.subjectgenetic analysis
dc.subjectgenetic model
dc.subjectgenetic polymorphism
dc.subjecthuman
dc.subjecthyperandrogenism
dc.subjecthyperhomocysteinemia
dc.subjecthyperlipidemia
dc.subjecthyperprolactinemia
dc.subjectinsulin resistance
dc.subjectmajor clinical study
dc.titleMthfr c677t polymorphism in turkish women with polycystic ovary syndrome; [Polikistik over sendromlu türk kadınlarında mthfr c677t polimorfizmi]
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.citation.trdizin1
rdl.citation.wos1
rdl.departmentT.C. SAĞLIK BAKANLIĞI
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexTRDIZIN
rdl.wos.indexEmerging Sources Citation Index (ESCI)