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dc.contributor.authorPercin, Ferda E.
dc.contributor.authorCetin, Meral
dc.contributor.authorPinarbasi, Ergun
dc.contributor.authorAkgun, Egemen
dc.contributor.authorGurlek, Fatma
dc.contributor.authorCetin, Ali
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:17:59Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:17:59Z
dc.date.issued2006
dc.identifier.issn0301-2115
dc.identifier.issn1872-7654
dc.identifier.urihttps://dx.doi.org/10.1016/j.ejogrb.2005.08.030
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10793
dc.descriptionWOS: 000240483600010en_US
dc.descriptionPubMed ID: 16303227en_US
dc.description.abstractObjectives: It is possible that altered control of aldosterone synthase gene (CYP11B2) expression or translation may be responsible for. hypertension. Hypertension is one of the major components of preeclampsia. We present here a study investigating the association between the CYP11B2 gene polymorphism in the promoter region at the position of -344 and preeclampsia. Study design: We analyzed a group of Turkish women for preeclampsia (n = 143), eclampsia (n = 36), and the HELLP syndrome (n = 55) and compared them with controls (n = 147). Genotypes for CYP11B2 were determined by polymerase chain reaction followed by digestion with BsuRI restriction enzyme. Results: The -344T/T, -344C/T, and -344C/C genotypes were found at comparable frequencies among the study groups, between the study and control groups, and between the study groups combined and the control group (p > 0.05). We combined the genotypes of TC and CC (polymorphic) and compared them with the TT (wild-type) genotype. There was no significant difference in the frequency of the TC plus CC genotypes among the study groups, between the study and control groups, and between the study groups combined and the control group (p > 0.05). There was no association of the CYP11B2 polymorphism among the preeclampsia, eclampsia, and HELLP groups and controls. Conclusions: The CYP11B2 gene polymorphism is not directly associated with preeclampsia, eclampsia, and the HELLP syndrome in women with these conditions. Therefore, this polymorphism may not be a risk factor for these disorders, at least not in the Turkish population. (C) 2005 Elsevier Ireland Ltd. All rights reserved.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.relation.isversionof10.1016/j.ejogrb.2005.08.030en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectpreeclampsiaen_US
dc.subjecteclampsiaen_US
dc.subjectHELLP syndromeen_US
dc.subjectCYP11B2 geneen_US
dc.subjectpolymorphismen_US
dc.titleLack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish womenen_US
dc.typearticleen_US
dc.relation.journalEUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGYen_US
dc.contributor.departmentGazi Univ, Sch Med, Dept Med Genet, TR-06500 Ankara, Turkey -- Cumhuriyet Univ, Sch Med, Dept Obstet, TR-58140 Sivas, Turkey -- Cumhuriyet Univ, Sch Med, Dept Med Biol, TR-58140 Sivas, Turkey -- Gazi Univ, Sch Med, Dept Med Genet, TR-58140 Sivas, Turkey -- Gazi Univ, Sch Med, Dept Gynecol, TR-58140 Sivas, Turkeyen_US
dc.contributor.authorIDPercin, Ferda -- 0000-0001-9317-8155; Cetin, Ali -- 0000-0002-5767-7894en_US
dc.identifier.volume127en_US
dc.identifier.issue2en_US
dc.identifier.endpage217en_US
dc.identifier.startpage213en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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