<?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>2026-06-29T07:37:13Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/99050" metadataPrefix="oai_dc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/99050</identifier><datestamp>2025-03-18T13:15:24Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</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>Simultaneous Assessment of Cardiac Inflammation and Extracellular Matrix Remodeling After Myocardial Infarction</dc:title>
   <dc:creator>Ramos, Isabel </dc:creator>
   <dc:creator>Henningsson, Markus</dc:creator>
   <dc:creator>Nezafat, Maryam</dc:creator>
   <dc:creator>Lavín Plaza, Begoña</dc:creator>
   <dc:creator>Lorrio, Silvia</dc:creator>
   <dc:creator>Gebhardt, Pierre</dc:creator>
   <dc:creator>Protti, Andrea</dc:creator>
   <dc:creator>Eykyn, Thomas </dc:creator>
   <dc:creator>Andia, Marcelo </dc:creator>
   <dc:creator>Floögel, Ulrich</dc:creator>
   <dc:creator>Phinikaridou, Alkystis</dc:creator>
   <dc:creator>Shah, Ajay </dc:creator>
   <dc:creator>Botnar, Reneé </dc:creator>
   <dc:subject>577.1</dc:subject>
   <dc:subject>Bioquímica (Química)</dc:subject>
   <dc:subject>24 Ciencias de la Vida</dc:subject>
   <dc:description>Background:
Optimal healing of the myocardium after myocardial infarction (MI) requires a suitable degree of inflammation and its timely resolution, together with a well-orchestrated deposition and degradation of ECM (extracellular matrix) proteins.
Methods and Results:
MI and SHAM-operated animals were imaged at 3, 7, 14, and 21 days with 3T magnetic resonance imaging using a 19F/1H surface coil. Mice were injected with 19F-perfluorocarbon nanoparticles to study inflammatory cell recruitment, and with a gadolinium-based elastin-binding contrast agent to evaluate elastin content. 19F magnetic resonance imaging signal colocalized with infarction areas, as confirmed by late gadolinium enhancement, and was highest 7 days post-MI, correlating with macrophage content (MAC-3 immunohistochemistry; ρ=0.89, P&lt;0.0001). 19F quantification with in vivo (magnetic resonance imaging) and ex vivo nuclear magnetic resonance spectroscopy correlated linearly (ρ=0.58, P=0.020). T1 mapping after gadolinium-based elastin-binding contrast agent injection showed increased relaxation rate (R1) in the infarcted regions and was significantly higher at 21 days compared with 7 days post-MI (R1 [s−1]: 21 days=2.8 [interquartile range, 2.69–3.30] versus 7 days=2.3 [interquartile range, 2.12–2.5], P&lt;0.05), which agreed with an increased tropoelastin content (ρ=0.89, P&lt;0.0001). The predictive value of each contrast agent for beneficial remodeling was evaluated in a longitudinal proof-of-principle study. Neither R1 nor 19F at day 7 were significant predictors for beneficial remodeling (P=0.68; P=0.062). However, the combination of both measurements (R1&lt;2.34 Hz and 0.55≤19F≤1.85) resulted in an odds ratio of 30.0 (CI 95%, 1.41–638.15; P=0.029) for favorable post-MI remodeling.
Conclusions:
Multinuclear 1H/19F magnetic resonance imaging allows the simultaneous assessment of inflammation and elastin remodeling in a murine MI model. The interplay of these biological processes affects cardiac outcome and may have potential for improved diagnosis and personalized treatment.</dc:description>
   <dc:description>Depto. de Bioquímica y Biología Molecular</dc:description>
   <dc:description>Fac. de Ciencias Químicas</dc:description>
   <dc:description>TRUE</dc:description>
   <dc:description>pub</dc:description>
   <dc:date>2024-02-05T15:12:07Z</dc:date>
   <dc:date>2024-02-05T15:12:07Z</dc:date>
   <dc:date>2018</dc:date>
   <dc:type>journal article</dc:type>
   <dc:type>AM</dc:type>
   <dc:identifier>https://hdl.handle.net/20.500.14352/99050</dc:identifier>
   <dc:identifier>1941-9651</dc:identifier>
   <dc:identifier>10.1161/circimaging.117.007453</dc:identifier>
   <dc:identifier>1942-0080</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Ramos, Isabel T., et al. «Simultaneous Assessment of Cardiac Inflammation and Extracellular Matrix Remodeling After Myocardial Infarction». Circulation: Cardiovascular Imaging, vol. 11, n.o 11, noviembre de 2018, p. e007453.  https://doi.org/10.1161/CIRCIMAGING.117.007453.</dc:relation>
   <dc:rights>open access</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>American Heart Association</dc:publisher>
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