<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-18T05:41:21Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10459.1/469667" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10459.1/469667</identifier><datestamp>2026-03-02T19:39:56Z</datestamp><setSpec>com_2072_3622</setSpec><setSpec>col_2072_479130</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Can NT-proBNP Enhance the Accuracy of Angiogenic Factors in the Short-Term Prediction of Preeclampsia?</dc:title>
   <dc:creator>Garrido Giménez, Carmen</dc:creator>
   <dc:creator>Nan, Madalina Nicoleta</dc:creator>
   <dc:creator>Cruz Lemini, Mónica</dc:creator>
   <dc:creator>García Manau, Pablo</dc:creator>
   <dc:creator>Garcia Osuna, Álvaro</dc:creator>
   <dc:creator>Ullmo, Johana</dc:creator>
   <dc:creator>Mora, Josefina</dc:creator>
   <dc:creator>Sánchez García, Olga</dc:creator>
   <dc:creator>Medina Mallén, Maria Del Carmen</dc:creator>
   <dc:creator>Chóliz, Marta</dc:creator>
   <dc:creator>Platero, Judit</dc:creator>
   <dc:creator>Llurba, Elisa</dc:creator>
   <dc:creator>Pelegay Escartín, Maria José</dc:creator>
   <dc:description>Background
Angiogenic biomarkers aid in short-term prediction of preeclampsia (PE) but are often limited by false-positive results. N-terminal pro–B-type natriuretic peptide (NT-proBNP), which is elevated in PE due to cardiovascular dysfunction, may enhance diagnostic precision. This study evaluated whether adding NT-proBNP to the soluble fms-like tyrosine kinase-1 (sFlt-1)/placental growth factor (PlGF) ratio improves prediction of PE and associated complications within 1 week.

Methods
We performed a prospective multicenter case-control study in pregnancies with suspected PE between 24 + 0 and 41 + 0 weeks. Three models evaluated the addition of NT-proBNP (cutoff ≥116 pg/mL) to the sFlt-1/PlGF ratio using thresholds &lt;38, ≥85, and 38 to 84. All models were assessed for early-onset, preterm, term, and overall PE prediction using receiver operating curve analysis, predictive metrics, and Kaplan–Meier survival curves.

Results
A total of 316 women (424 serum samples) were included. PE occurred in 23.4% of cases, including 8.5% early-onset PE. NT-proBNP levels were significantly elevated in PE cases. The addition of NT-proBNP improved early-onset PE prediction, particularly in intermediate-risk cases (sFlt-1/PlGF 38–84), achieving an area under the curve (AUC) of 0.949 and a negative predictive value (NPV) of 99.5%, outperforming sFlt-1/PlGF alone. Survival analysis revealed a shorter median time to delivery when both biomarkers were elevated (1.3 vs 4.0 weeks; P &lt; 0.001). For term PE, NT-proBNP increased positive predictive value when combined with sFlt-1/PlGF ≥ 38. In complicated PE, the combined model improved specificity (77.4%) and AUC (0.770), with an NPV of 91.1%.

Conclusions
NT-proBNP enhances the short-term predictive performance of the sFlt-1/PlGF ratio, particularly in intermediate-risk cases. This multimarker approach may refine risk stratification and support timely clinical intervention in pregnancies at risk of PE.</dc:description>
   <dc:date>2026-01</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>https://doi.org/10.1093/clinchem/hvaf135</dc:identifier>
   <dc:identifier>1530-8561</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10459.1/469667</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10459.1/469667</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a https://doi.org/10.1093/clinchem/hvaf135</dc:relation>
   <dc:relation>Clinical Chemistry, 2026, vol. 72, núm. 1, p. 206-216</dc:relation>
   <dc:rights>cc-by-nc-nd, (c) Carmen Garrido Giménez et al., 2026</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:publisher>Oxford University Press</dc:publisher>
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