Publication:
Is Afamin a Potential Early Biomarker for Subsequent Development of Preeclampsia? A Nested Case-Control Study

dc.authorscopusid57205129081
dc.authorscopusid57198130901
dc.authorscopusid6603017389
dc.authorwosidSoyer Caliskan, Canan/Jvm-8613-2024
dc.authorwosidAvci, Bahattin/C-1877-2012
dc.contributor.authorCaliskan, Canan Soyer
dc.contributor.authorCelik, Samettin
dc.contributor.authorAvci, Bahattin
dc.date.accessioned2025-12-11T00:42:23Z
dc.date.issued2021
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Caliskan, Canan Soyer; Celik, Samettin] Training & Res Hosp, TR-55090 Samsun, Turkey; [Avci, Bahattin] Ondokuz Mayis Univ, Fac Med, Biochem, Samsun, Turkeyen_US
dc.description.abstractObjective The objective of this study is to determine if the second-trimester serum afamin is a reasonable predictor of preeclampsia (PE). Methods In this nested case-control study, all pregnant women were screened by second-trimester screening test between 15 and 20 weeks of gestation and serum samples were collected and stored at -80 degrees C for biochemical analysis. All available stored samples from pregnant women who subsequently developed PE were thawed and the concentrations of afamin in the serum were measured. Control cases, chosen randomly from the same cohort whose blood was collected and stored in the same period as with the study group, who did not develop PE. Afamin levels were expressed ng/mL. Logistic regression was used to calculate adjusted odds ratio (aORs) for the prediction of PE. Results A total of 39 women with PE and 46 controls were studied. Afamin levels were found to be significantly higher during the second trimester in women who developed PE compared to the control group. Afamin, at a cut-off level of 96.2 ng/mL, the aORs for PE was 28.6 (95% CI: 7.458-110.193). After adjustment for BMI, age, smoking, the aORs for PE was 65.6 (95% CI: 11.6-371.4;p= .001). Conclusion High levels of afamin in the early weeks of gestation in patients going on to develop PE later may be promising as a potential marker to predict PE in the first and second trimesters.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1080/14767058.2020.1818201
dc.identifier.endpage2011en_US
dc.identifier.issn1476-7058
dc.identifier.issn1476-4954
dc.identifier.issue12en_US
dc.identifier.pmid33028116
dc.identifier.scopus2-s2.0-85092361862
dc.identifier.scopusqualityQ2
dc.identifier.startpage2006en_US
dc.identifier.urihttps://doi.org/10.1080/14767058.2020.1818201
dc.identifier.urihttps://hdl.handle.net/20.500.12712/38607
dc.identifier.volume34en_US
dc.identifier.wosWOS:000575968600001
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofJournal of Maternal-Fetal & Neonatal Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAfaminen_US
dc.subjectPreeclampsiaen_US
dc.subjectPregnancyen_US
dc.subjectPredictionen_US
dc.titleIs Afamin a Potential Early Biomarker for Subsequent Development of Preeclampsia? A Nested Case-Control Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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