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Verification of placental growth factor and soluble-fms-like tyrosine kinase 1 assay performance in late pregnancy and their diagnostic test accuracy in women with reduced fetal movement

Authors :
Alexander E. P. Heazell
Tim James
Shonagh Haslam
Lindsay Armstrong-Buisseret
Lucy Bradshaw
Source :
Armstrong-Buisseret, L K, Haslam, S, James, T, Bradshaw, L & Heazell, A 2020, ' Verification of Placental Growth Factor and Soluble-fms-like Tyrosine Kinase 1 Assay Performance in Late Pregnancy and their Diagnostic Test Accuracy in Women with Reduced Fetal Movement ', Annals of Clinical Biochemistry . https://doi.org/10.1177/0004563220911993
Publication Year :
2020
Publisher :
SAGE Publications, 2020.

Abstract

Background Placental growth factor (PlGF) and soluble-fms-like tyrosine kinase 1 (sFlt-1) are biomarkers of placental function used to aid the diagnosis and prediction of pregnancy complications. This work verified the analytical performance of both biomarkers and provides preliminary diagnostic accuracy data to identify adverse pregnancy outcome in women with reduced fetal movement. Methods Verification of sFlt-1 and PlGF assays included a comparative accuracy assessment of 24 serum samples analysed at six different sites and laboratory-specific precision estimates. The sFlt-1/PlGF ratio was assessed in serum samples obtained prospectively from 295 women with reduced fetal movement ≥36 weeks’ gestation; diagnostic accuracy was evaluated using 2 × 2 tables and area under the receiver operator characteristic (AUROC) curve. Results Regression analysis showed that performance between sites was good with Passing-Bablok slopes ranging from 0.96 to 1.05 (sFlt-1) and 0.93 to 1.08 (PlGF). All sites had a mean bias Conclusions Analytical performance of the sFlt-1 and PlGF assays was comparable across different sites. The sensitivity of sFlt-1/PlGF to identify adverse pregnancy outcome in women with reduced fetal movement was considered acceptable, in the absence of other tests, to progress to a pilot randomized controlled trial.

Details

ISSN :
17581001 and 00045632
Volume :
57
Database :
OpenAIRE
Journal :
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine
Accession number :
edsair.doi.dedup.....afeef7ec7435fa2318634c17c649abc1
Full Text :
https://doi.org/10.1177/0004563220911993