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Maternal placental growth factor and soluble fms-like tyrosine kinase-1 reference ranges in post-term pregnancies: A prospective observational study

BACKGROUND: Post-term pregnancies have increased risks for adverse fetal and maternal outcomes. Maternal concentrations of the placenta-associated proteins placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) have been identified as predictors for preeclampsia and fetal gro...

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Detalles Bibliográficos
Autores principales: Mitlid-Mork, Birgitte, Bowe, Sophie, Gran, Jon M., Bolstad, Nils, Berg, Jens Petter, Redman, Christopher W., Staff, Anne Cathrine, Sugulle, Meryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575115/
https://www.ncbi.nlm.nih.gov/pubmed/33079955
http://dx.doi.org/10.1371/journal.pone.0240473
Descripción
Sumario:BACKGROUND: Post-term pregnancies have increased risks for adverse fetal and maternal outcomes. Maternal concentrations of the placenta-associated proteins placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) have been identified as predictors for preeclampsia and fetal growth restriction, both syndromes of placental dysfunction. We have proposed that low maternal circulating PlGF and increased sFlt-1 are general markers for syncytiotrophoblast stress, which increases at and beyond term, even in apparently uncomplicated pregnancies. Our aim was to establish circulating PlGF, sFlt-1, and sFlt-1/PlGF reference ranges in healthy post-term pregnancies (gestational week ≥40(+2)), comparing with healthy term pregnancies and evaluating associations between time to delivery and biomarker percentiles. METHODS: Of 501 healthy, singleton post-term pregnancies prospectively recruited between September 2016 and December 2017 at our tertiary obstetric department, 426 with an uncomplicated delivery outcome contributed PlGF and sFlt-1 serum concentrations for reference range construction. A retrospective, cross-sectional, term group with an uncomplicated delivery outcome (n = 146) served as comparison. Differences in percentile values between groups and confidence intervals were calculated by quantile regression. RESULTS: In post-term pregnancies the 5(th), 50(th), and 95(th) percentiles for PlGF were: 70, 172, and 496 pg/mL; for sFlt-1: 2074, 4268, and 9141 pg/mL; and for sFlt-1/PlGF 5.3, 25.5, and 85.2. Quantile regression analyses comparing the post-term to the term group showed for PlGF a trend towards higher 10(th) through 30(th) percentiles, for sFlt-1 significantly higher 10(th) through 80(th) percentiles, and for sFlt-1/PlGF ratio significantly higher 30(th) percentile and significantly lower 95(th) percentile. PlGF below the 5(th) percentile and sFlt-1/PlGF ratio above the 95(th) percentile was associated with shorter time to delivery (p = 0.031 and p = 0.025, respectively). CONCLUSIONS: Our findings support the concept of increasing syncytiotrophoblast stress post-term in clinically healthy pregnancies. Whether post-term dysregulated angiogenic markers reflect a biological placental clock merits further investigation.