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dc.contributor.authorSancak, Eyüp Burak
dc.contributor.authorOğuz, Sevilay
dc.contributor.authorAkbulut, Tuğba
dc.contributor.authorUludağ, Ayşegül
dc.contributor.authorAkbaş, Alpaslan
dc.contributor.authorKurt, Ömer
dc.contributor.authorAkbulut, Mehmet Fatih
dc.date.accessioned2022-05-11T14:36:59Z
dc.date.available2022-05-11T14:36:59Z
dc.date.issued2016
dc.identifier.issn1911-6470
dc.identifier.issn1920-1214
dc.identifier.urihttps://doi.org/10.5489/cuaj.3582
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8515
dc.description.abstractIntroduction: We sought to evaluate the association of female sexual dysfunction (FSD) with androgenetic alopecia (AGA) and metabolic syndrome (MetS) in premenopausal women. Methods: From December 2013 to June 2015, we performed a case-control, prospective study of 115 patients with AGA and 97 age-matched control patients without AGA from among premenopausal women who visited dermatology clinics of the two reference hospitals. Comprehensive history, anthropometric measurements, and questionnaire administration were performed for each of the total of 212 women. The Female Sexual Function Index (FSFI) was used to assess the key dimensions of female sexual function. AGA was assessed and graded by an experienced dermatologist according to Ludwig's classification. The MetS assessment was made according to the NCEP-ATP III criteria. Results: In univariate analysis, age, weight, waist circumference, hip circumference, waist-to-hip ratio, body mass index (BMI), AGA, MetS, cardiovascular event, marital status, hypertension, high fasting plasma glucose, high triglyceride, large waist, total testosterone, and free testosterone were associated with presence of FSD. In logistic regression analysis, age (odds ratio [OR] 1.21, 95% confidence interval [CI] 1.13. 1.30; p<0.001), AGA (OR 3.42, 95% CI 1.31. 8.94; p= 0.017), MetS (OR 5.39, 95% CI 1.34. 21.62; p= 0.012), and free testosterone (OR 0.18, 95% CI 0.09. 0.37; p< 0.001) were independently associated with FSD. Conclusions: Our study suggests that age, AGA, MetS, and free testosterone may have strong impact on sexual function in premenopausal women. Further studies with population-based and longitudinal design should be conducted to confirm this finding.en_US
dc.language.isoengen_US
dc.publisherCanadian Urological Associationen_US
dc.identifier.doi10.5489/cuaj.3582
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMiddle-Aged Womenen_US
dc.subjectMetabolic Syndromeen_US
dc.subjectInsulin-Resistanceen_US
dc.subjectRisk-Factorsen_US
dc.subjectIndex Fsfien_US
dc.subjectTestosteroneen_US
dc.subjectPrevalenceen_US
dc.subjectAssociationen_US
dc.subjectTherapyen_US
dc.subjectMenen_US
dc.titleFemale sexual dysfunction in androgenetic alopecia: Case-control studyen_US
dc.typearticleen_US
dc.relation.ispartofCuaj-Canadian Urological Association Journalen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Üroloji Ana Bilim Dalıen_US
dc.authorid0000-0002-5007-8143
dc.authorid0000-0003-1470-5952
dc.identifier.volume10en_US
dc.identifier.issue7-8en_US
dc.identifier.startpageE251en_US
dc.identifier.endpageE256en_US
dc.institutionauthorKurt, Ömer
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid55753628300
dc.authorscopusid55749960900
dc.authorscopusid57194558922
dc.authorscopusid55647897100
dc.authorscopusid23977731600
dc.authorscopusid57216014831
dc.authorscopusid56841316400
dc.authorwosidAkbulut, Tugba Özkök/AAM-5899-2021
dc.authorwosidAkbulut, Mehmet Fatih/N-3886-2019
dc.authorwosidAkbas, Alpaslan/AAX-5617-2020
dc.identifier.wosWOS:000382528100008en_US
dc.identifier.scopus2-s2.0-84978173620en_US
dc.identifier.pmid28255417en_US


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