Serum soluble fms‐like tyrosine kinase‐1 in the three trimesters of pregnancy: effects of maternal characteristics and medical history. (30th March 2015)

• Record Type: Journal Article
• Authors: Tsiakkas, A.; Duvdevani, N.; Wright, A.; Wright, D.; Nicolaides, K. H.
• Is Part Of: Ultrasound in obstetrics & gynecology. Volume 45:Number 5(2015:May)
• Page Start: 584
• Page End: 590
• Publication Date: 2015-03-30
• Subjects: first‐trimester screening -- pre‐eclampsia -- pyramid of pregnancy care -- sFlt‐1 -- second‐trimester screening -- soluble fms‐like tyrosine kinase‐1 -- third‐trimester screening -- trisomy 21; Ultrasonics in obstetrics -- Periodicals; Generative organs, Female -- Diseases -- Diagnosis -- Periodicals; Diagnosis, Ultrasonic -- Periodicals; Genital Diseases, Female -- ultrasonography -- Periodicals; Ultrasonography, Prenatal -- Periodicals; 618.047543
• DOI: 10.1002/uog.14817
• Languages: English
• ISSNs: 0960-7692

Abstract

ABSTRACT: Objective: To define the contribution of maternal variables which influence the measured level of maternal serum soluble fms‐like tyrosine kinase‐1 (sFlt‐1) in screening for pregnancy complications. Methods: Maternal characteristics and medical history were recorded and serum sFlt‐1 was measured in women with a singleton pregnancy attending for three routine hospital visits at 11 + 0 to 13 + 6, 19 + 0 to 24 + 6 and 30 + 0 to 34 + 6 or 35 + 0 to 37 + 6 weeks' gestation. For pregnancies delivering phenotypically normal live births or stillbirths ≥ 24 weeks' gestation, variables from maternal demographic characteristics and medical history that are important in the prediction of sFlt‐1 were determined from a linear mixed‐effects multiple regression. Results: Serum sFlt‐1 was measured in 7066 cases in the first trimester, 8078 in the second trimester and 10 464 in the third trimester. Significant independent contributions to serum sFlt‐1 were provided by gestational age, maternal weight, racial origin, cigarette smoking, birth‐weight Z ‐score of the neonate in the previous pregnancy and interpregnancy interval. Random‐effects multiple regression analysis was used to define the contribution of maternal variables that influence the measured level of serum sFlt‐1 and express the values as multiples of the median (MoMs). The model was shown to provide an adequate fit of MoM values for all covariates, both in pregnancies that developed pre‐eclampsia and in those without this pregnancy complication. Conclusions: A model was fitted to express measured serum sFlt‐1 across the three trimesters of pregnancy as MoMs, after adjusting for variables from maternal characteristics and medical history that affect this measurement. Copyright © 2015 ISUOG. Published by John Wiley & Sons Ltd.