<?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>2026-04-29T06:15:48Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/15652" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/15652</identifier><datestamp>2025-04-24T18:35:50Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_15322</setSpec><setSpec>col_20.500.12105_19605</setSpec><setSpec>col_20.500.12105_16977</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Martínez-Milla, Juan</subfield>
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      <subfield code="a">Aceña, Álvaro</subfield>
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      <subfield code="a">Pello, Ana</subfield>
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      <subfield code="a">López-Castillo, Marta</subfield>
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      <subfield code="a">Gaebelt, Hans Paul</subfield>
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      <subfield code="a">González-Lorenzo, Óscar</subfield>
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      <subfield code="a">Tarín, Nieves</subfield>
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      <subfield code="a">Cristóbal, Carmen</subfield>
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      <subfield code="a">Blanco-Colio, Luis M</subfield>
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      <subfield code="a">Martín-Ventura, José Luis</subfield>
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      <subfield code="a">Kallmeyer, Andrea</subfield>
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      <subfield code="a">Alonso, Joaquín</subfield>
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      <subfield code="a">Gutiérrez-Landaluce, Carlos</subfield>
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      <subfield code="a">López Bescós, Lorenzo</subfield>
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      <subfield code="a">Egido, Jesús</subfield>
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      <subfield code="a">Mahíllo-Fernández, Ignacio</subfield>
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      <subfield code="a">Lorenzo, Óscar</subfield>
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      <subfield code="a">González-Casaus, María Luisa</subfield>
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      <subfield code="a">Tuñón, José</subfield>
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      <subfield code="a">Mahillo-Fernandez, Ignacio</subfield>
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      <subfield code="c">2022-07-17</subfield>
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      <subfield code="a">Background. Mineral metabolism (MM) system and N-terminal pro-brain natriuretic peptide (NT-ProBNP) have been shown to add prognostic value in patients with stable coronary artery disease (SCAD). However, the influence of NT-ProBNP on the prognostic role of MM in patients with SCAD has not been shown yet. The objective of this study is to assess the influence of NT-ProBNP on the prognostic role of MM markers in patients with SCAD. Methods: We analyzed the prognostic value of MM markers (parathormone (PTH), klotho, phosphate, calcidiol (25-hydroxyvitamin D3), and fibroblast growth factor-23) in 964 patients with SCAD and NT-ProBNP > 125 pg/mL vs. patient with NT-ProBNP ≤ 125 pg/mL included in five hospitals in Spain. The main outcome was the combination of death, heart failure, and ischemic events (any acute coronary syndrome, ischemic stroke, or transient ischemic attack). Results: A total of 622 patients had NT-proBNP > 125 pg/mL and 342 patients had NT-ProBNP ≤ 125 pg/mL. The median follow-up was 5.1 years. In the group of NT-proBNP > 125 pg/mL, the patients were older, and there were more females and smokers than in the group of patients with normal NT-proBNP. Additionally, the proportion of patients with hypertension, atrial fibrillation, ejection fraction &lt; 40%, cerebrovascular attack, or prior coronary artery bypass graft was higher in the high NT-proBNP group. In the high NT-proBNP patients, the predictors of poor prognosis were PTH (HR = 1.06 (1.01−1.10), p &lt; 0.001) and NT-proBNP (HR = 1.02 (1.01−1.03), p = 0.011), along with age (HR = 1.039 (1.02−1.06), p &lt; 0.001), prior coronary artery bypass graft (HR = 1.624 (1.02−2.59), p = 0.041), treatment with statins (HR = 0.32 (0.19−0.53), p &lt; 0.001), insulin (HR = 2.49 (1.59−4.09), p &lt; 0.001), angiotensin receptor blockers (HR = 1.73 (1.16−2.56), p = 0.007), nitrates (HR = 1.65 (1.10−2.45), p = 0.014), and proton pump inhibitors (HR = 2.75 (1.74−4.36), p &lt; 0.001). In the NT-proBNP ≤ 125 pg/mL subgroup, poor prognosis predictors were plasma levels of non-high-density lipoprotein (non-HDL) cholesterol (HR = 1.01 (1.00−1.02), p = 0.014) and calcidiol (HR = 0.96 (0.92−0.99), p = 0.045), as well as treatment with verapamil (HR = 11.28 (2.54−50.00), p = 0.001), and dihydropyridines (HR = 3.16 (1.63−6.13), p = 0.001). Conclusion: In patients with SCAD and NT-ProBNP > 125 pg/mL, PTH and NT-ProBNP, which are markers related to ventricular damage, are predictors of poor outcome. In the subgroup of patients with NT-ProBNP ≤ 125 pgm/L, calcidiol and non-HDL cholesterol, which are more related to vascular damage, are the independent predictors of poor outcome. Then, in patients with SCAD, baseline NT-ProBNP may influence the type of biomarker that is effective in risk prediction.</subfield>
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      <subfield code="a">J Clin Med. 2022 Jul 17;11(14):4153</subfield>
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      <subfield code="a">2077-0383</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/15652</subfield>
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      <subfield code="a">35887917</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.3390/jcm11144153</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Journal of clinical medicine</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">NT-proBNP Levels Influence the Prognostic Value of Mineral Metabolism Biomarkers in Coronary Artery Disease.</subfield>
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