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dc.contributor.authorAkar, Bertan
dc.contributor.authorKöle, Emre
dc.contributor.authorÖzcan, Canan
dc.contributor.authorÇakır Köle, Merve
dc.date.accessioned2023-05-26T08:05:29Z
dc.date.available2023-05-26T08:05:29Z
dc.date.issued2022en_US
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1142045/do-the-levels-of-cffdna-fraction-change-in-pregnancies-with-placental-problems
dc.identifier.urihttps://hdl.handle.net/20.500.12868/2191
dc.description.abstractObjective: To investigate the value of the cell free fetal DNA (cffDNA) for determining the important obstetric complications such as preeclampsia, intrauterine growth retardation (IUGR) and, preterm labor other than prenatal screening of fetal aneuploidies. Methods: Our single center- retrospective study included 131 pregnant women in their 10-24th weeks of gestation, between the dates September 2019 and March 2020 who applied for cffDNA analysis (HarmonyTM Prenatal Test; Ariosa Diagnostics Inc., San Jose, Calif., USA) with indications including advanced maternal age (≥40) and high risk for trisomy 13.18 and 21 according to the results of the first trimester prenatal screening or solely on their own desire. Results: Oligohydraamnios was observed in 10 (8.1%) patients, gestational diabetes in 10 patients (8.1%), preeclampsia in 7 (8.6%) patients and ablatio plasenta in 2 (1.2%) patients in this study. Increasing levels of the extracellular fetal DNA fractions in 10-24th gestational weeks showed statistically significant correlation for predicting the risk for IUGR (p<0.01). There was not a statistically significant difference between the level of extracellular fetal DNA fractions and the other obstetric complications (preeclampsia, preterm labor, GDM, oligohydraamnios). Conclusion: Although cff-DNA has many valuable implications as a novel biomarker for prenatal screening for special fetal aneuploidies, the association between the levels of cff-DNA and the risk of obstetric complications in clinical practice has not been clarified yet . Further studies should aim to investigate the cff-DNA levels in patients with pathological obstetric conditions in order to detect its potential predictive value and diagnostic implementation.en_US
dc.language.isoengen_US
dc.relation.isversionof10.53446/actamednicomedia.1173411en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectcffDNAen_US
dc.subjectPregnancyen_US
dc.subjectPlacentaen_US
dc.subjectPregnancy Outcomesen_US
dc.subjectGebeliken_US
dc.subjectPlasentaen_US
dc.subjectGebelik Sonuçlarıen_US
dc.titleDo the Levels of cffDNA Fraction Change in Pregnancies with Placental Problems?en_US
dc.typearticleen_US
dc.contributor.departmentALKÜ, Fakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.identifier.volume5en_US
dc.identifier.issue3en_US
dc.identifier.startpage176en_US
dc.identifier.endpage180en_US
dc.relation.journalActa Medica Nicomediaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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