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dc.contributor.authorGunday, O. K.
dc.contributor.authorVurmaz, A.
dc.contributor.authorYilmazer, M.
dc.date.accessioned2025-12-28T16:41:02Z
dc.date.available2025-12-28T16:41:02Z
dc.date.issued2025
dc.identifier.issn1210-7832
dc.identifier.issn1805-4455
dc.identifier.urihttps://doi.org/10.48095/cccg2025212
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2801
dc.description.abstractObjective: We aimed to evaluate the usefulness of serum kisspeptin (KP), measured in the 1(st) trimester (11- 14 weeks), as a new biomarker that can predict antenatal complications. Materials and methods: A prospective case-control study of prospectively collected data. Blood samples of all patients (N = 124) were preserved at - 70 degrees C for the assessment of serum KP-10 and KP-54 levels. The KP levels were analyzed for comparison among women who experienced complications including fetal growth retardation (FGR), pregnancy-induced hypertension (PIH), preterm delivery, gestational diabetes, and fetal death. The control group consisted of matching subjects who completed their pregnancies without problems. The predictive eff ect of serum KP on adverse pregnancy outcomes was investigated. Results: Among all adverse pregnancy outcomes, the KP-10 level was signifi cantly higher in patients who developed FGR (P = 0.025). In the patient cohort aff ected by PIH, either accompanied by preeclampsia or standalone, there was a trend towards higher KP-10 levels (P = 0.059), although statistical signifi cance was not achieved. However, regarding KP-10, the calculated cut-off value and the area under the curve (AUC) for predicting the onset of FGR were statistically signifi cant (AUC: 0.684; P = 0.006). The model established with KP-10, PIH, and pregnancy associated plasma protein-A (PAPP-A) was found to be signifi cant in predicting the development of FGR (P = 0.006; NPV: 98%; PPV: 21.4%; OR: 0.10; 95% CI 0.016- 0.611). Conclusions: First trimester maternal serum KP levels may have the potential to be used as a 1(st) trimester bio marker that can predict the development of FGR.
dc.language.isoen
dc.publisherNakladatelske Stredisko C L S J E Purkyne
dc.relation.ispartofCeska Gynekologie-Czech Gynaecology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectkisspeptin-10
dc.subjectkisspeptin-54
dc.subjectpregnancy outcome
dc.subjectfetal growth restriction
dc.subjectpregnancy-induced hypertension
dc.titleThe association between 1st trimester serum kisspeptin level and antenatal complications
dc.title.alternativeSouvislost mezi hladinou kisspeptinu v séru v I. trimestru a prenatálními komplikacemi
dc.typeArticle
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.48095/cccg2025212
dc.identifier.volume90
dc.identifier.issue3
dc.identifier.startpage212
dc.identifier.endpage221
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Gunday, O. K.; Yilmazer, M.] Afyonkarahisar Univ Hlth Sci, Fac Med, Dept Obstet & Gynecol, Afyon, Turkiye; [Vurmaz, A.] Afyonkarahisar Univ Hlth Sci, Fac Med, Dept Biochem, Afyon, Turkiye
dc.identifier.pmid40663448
dc.identifier.scopus2-s2.0-105011773950
dc.identifier.scopusqualityQ3
dc.identifier.wosWOS:001532557900001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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