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dc.contributor.authorSujinun Nunthapiwaten_US
dc.contributor.authorRatanaporn Sekararithien_US
dc.contributor.authorChanane Wanapiraken_US
dc.contributor.authorSupatra Sirichotiyakulen_US
dc.contributor.authorFuanglada Tongpraserten_US
dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorSuchaya Luewanen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2019-08-05T04:40:05Z-
dc.date.available2019-08-05T04:40:05Z-
dc.date.issued2019-07-01en_US
dc.identifier.issn1423002Xen_US
dc.identifier.issn03787346en_US
dc.identifier.other2-s2.0-85059551104en_US
dc.identifier.other10.1159/000495614en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059551104&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/65722-
dc.description.abstract© 2019 S. Karger AG, Basel. All rights reserved. Objective: To determine the association between second-trimester serum Down syndrome screening (alpha-fetoprotein [AFP] free beta-human chorionic gonadotropin [b-hCG] unconjugated estriol [uE3]) and preterm birth and to create predictive models for preterm birth. Methods: Secondary analysis on a prospective database of pregnancies undergoing second-trimester screen with complete follow-up. The multiples of medians (MoM) of the biomarkers were compared between the group of term, preterm (< 37 weeks), early preterm (< 34 weeks), and very early preterm (< 32 weeks) delivery. Predictive models were developed based on adjusted MoMs and logistic regression and diagnostic performances in predicting preterm birth were determined. Results: Of 20,780 pregnancies, 1,554 (7.5), 363 (1.7), and 158 (0.8%) had preterm, early preterm, and very early preterm birth respectively. High levels of AFP and b-hCG but low levels of uE3 were significantly associated with higher rates of preterm, early preterm and very early preterm delivery. The predictive models had diagnostic performance in predicting preterm birth with the areas under the ROC curve of 0.688, 0.534, 0.599, and 0.718 for AFP, b-hCG, uE3, and combined biomarkers respectively. Conclusion: The second trimester Down syndrome screening could also be used as a tool of risk identification of preterm birth in the same test, without extra-effort and extra-cost.en_US
dc.subjectMedicineen_US
dc.titleSecond Trimester Serum Biomarker Screen for Fetal Aneuploidies as a Predictor of Preterm Delivery: A Population-Based Studyen_US
dc.typeJournalen_US
article.title.sourcetitleGynecologic and Obstetric Investigationen_US
article.volume84en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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