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Comparison of glycosylated fibronectin versus soluble fms-like tyrosine kinase/placental growth factor ratio testing for the assessment of pre-eclampsia: protocol for a multicentre diagnostic test accuracy study.

Elbarbary, N; Wang, C; Ganapathy, R; Green, M; Fisher, S; Thilaganathan, B; Bhide, A (2025) Comparison of glycosylated fibronectin versus soluble fms-like tyrosine kinase/placental growth factor ratio testing for the assessment of pre-eclampsia: protocol for a multicentre diagnostic test accuracy study. BMJ Open, 15 (1). e093586. ISSN 2044-6055 https://doi.org/10.1136/bmjopen-2024-093586
SGUL Authors: Thilaganathan, Baskaran Bhide, Amarnath

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Abstract

INTRODUCTION: Pre-eclampsia is a condition associated with significant maternal and neonatal morbidity and mortality. The prediction of pre-eclampsia in high-risk populations using angiogenic markers, such as serum placental growth factor (PlGF) assessment, has been shown to improve maternal outcomes and is recommended by the National Institute for Health and Care Excellence (NICE). However, such tests are not yet available at the point of care (POC). Glycosylated fibronectin (GlyFn) level for the prediction of pre-eclampsia development is available as a POC test (Lumella) and has the potential to aid rapid clinical decision making. This study aimed to test the hypothesis that the sensitivity of the GlyFn test is not inferior to that of the current gold standard of soluble fms-like tyrosine kinase (sFlt)/PlGF-based laboratory testing for pre-eclampsia. METHODS AND ANALYSIS: This is a multicentre prospective study. Women at risk for pre-eclampsia based on predefined clinical and/or obstetric risk factors will be invited to participate in the study. The recruitment target is 400 participants. Consenting participants will have paired samples for sFlt/PlGF together with POC GlyFn testing. Two follow-up visits are planned at 2 and 4 weeks after the initial recruitment where repeat testing with both tests will be performed. The clinical team will be blinded to the results of the GlyFn test but not that of the sFlt/PlGF test. Clinical care will be based on established protocols incorporating maternal/fetal evaluation and the results of sFlt/PlGF levels. Maternal and neonatal outcome data will be collected to compare the sensitivity and specificity of the tests, with the primary outcome being delivery for pre-eclampsia within 4 weeks. ETHICS AND DISSEMINATION: Ethical approval has been obtained from the Health Research Authority and Health and Care Research Wales Ethics Committee. The results of this study will be published in peer-reviewed journals and presented at scientific conferences. TRIAL REGISTRATION NUMBER: ISRCTN13430018.

Item Type: Article
Additional Information: © Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY. Published by BMJ Group. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
Keywords: Fetal medicine, Maternal medicine, OBSTETRICS, Pregnancy, Humans, Pre-Eclampsia, Pregnancy, Female, Fibronectins, Placenta Growth Factor, Biomarkers, Prospective Studies, Vascular Endothelial Growth Factor Receptor-1, Sensitivity and Specificity, Adult, Multicenter Studies as Topic, Glycated Proteins, Humans, Pre-Eclampsia, Vascular Endothelial Growth Factor Receptor-1, Fibronectins, Sensitivity and Specificity, Prospective Studies, Pregnancy, Adult, Female, Multicenter Studies as Topic, Biomarkers, Placenta Growth Factor, Glycated Proteins, Pregnancy, OBSTETRICS, Fetal medicine, Maternal medicine, 1103 Clinical Sciences, 1117 Public Health and Health Services, 1199 Other Medical and Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Cardiovascular & Genomics Research Institute
Academic Structure > Cardiovascular & Genomics Research Institute > Clinical Cardiology
Academic Structure > Cardiovascular & Genomics Research Institute > Vascular Biology
Journal or Publication Title: BMJ Open
ISSN: 2044-6055
Language: eng
Dates:
DateEvent
2 February 2025Published
10 January 2025Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
NIHR204647National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 39894517
Web of Science ID: WOS:001413275300001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/117191
Publisher's version: https://doi.org/10.1136/bmjopen-2024-093586

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