Clinical utility of a glycosylated fibronectin test (LumellaTM) for assessment of impending preeclampsia
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Observational Study, Multicenter Study
- Keywords
- Glycosylated fibronectin, diagnosis, preeclampsia, preterm birth, screening,
- MeSH
- Biomarkers analysis MeSH
- Adult MeSH
- Fibronectins * analysis MeSH
- Gestational Age MeSH
- Glycated Proteins MeSH
- Immunoassay methods MeSH
- Humans MeSH
- Pilot Projects MeSH
- Point-of-Care Testing MeSH
- Predictive Value of Tests MeSH
- Pre-Eclampsia * diagnosis MeSH
- Prospective Studies MeSH
- Pregnancy MeSH
- Point-of-Care Systems MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Pregnancy MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Names of Substances
- Biomarkers MeSH
- Fibronectins * MeSH
- glycated fibronectin MeSH Browser
- Glycated Proteins MeSH
OBJECTIVE: Preeclampsia is a major pregnancy complication that results in significant maternal and infant mortality and morbidity, yet difficulties remain in the diagnosis of preeclampsia based on clinical parameters alone. The objective was to assess the performance of a hand-held point-of-care (POC) immunoassay in a clinical environment for glycosylated fibronectin (GlyFn) for the prediction of preeclampsia within 4 weeks of sampling. METHODS: Multinational European prospective observational pilot study of predominantly high-risk patients in the second half of pregnancy to assess a point-of-care immunoassay for GlyFn in predicting preeclampsia within 4 weeks of sampling. GlyFn was measured using a second generation hand held POC immunoassay. Results were considered normal for GlyFn concentrations of < 350 µg/mL, positive for GlyFn concentrations of 351-600 µg/mL, and high-positive for GlyFn concentrations > 600 µg/mL. RESULTS: Preeclampsia developed in 16 (19%) of 84 subjects and was associated with a shorter gestational age at delivery 35.3 weeks vs. 37.3 weeks for non-preeclamptics, n = 82; p = 0.001), a higher risk of fetal growth restriction (FGR; 31.2% vs. 10.3% for non-preeclamptics, p = 0.046), and an increased risk of preterm birth < 37 weeks gestation (83.3% vs. 33.3% for non-preeclamptics, (n = 78; p = 0.003). GlyFn positive or high positive was seen in 13/16 (81%) and in 35/68 (51.5%), yielding a sensitivity of 81%, a specificity of 49%, a positive predictive value of 27%, and a negative predictive value of 92%. GlyFn positive or high positive was also associated with preterm birth < 37 weeks in singleton pregnancy non-preeclamptic patients. Preterm birth occurred in 4.8% of those with normal GlyFn, in 26.7% with positive GlyFn, and in 50% of those with high GlyFn in singleton gestations without preeclampsia (p = 0.008). CONCLUSION: The ability to use this test in a POC format provides a method for practitioners to quickly determine risk for preeclampsia in their pregnant patients and offers an affordable alternative, as a single analyte to other diagnostic or screening tests that require laboratory-based testing or ultrasound equipment. Independent of preeclampsia, an elevated GlyFn was also correlated with preterm delivery and requires further study.
Biomedical Research Center University Hospital Hradec Králové Hradec Králové Czech Republic
Department of Obstetrics and Gynecology Bordeaux University Hospital Bordeaux France
Department of Obstetrics and Gynecology Hospital Most Ústí nad Labem Czech Republic
Department of Obstetrics and Gynecology Medical University of Warsaw Warsaw Poland
Obstetrics and Gynecology Department S Maria della Misericordia Hospital Perugia Italy
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