<?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>2026-06-14T02:01:33Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/8351" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/8351</identifier><datestamp>2024-09-27T09:44:36Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</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">dc</subfield>
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      <subfield code="a">Fernandez-Friera, Leticia</subfield>
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      <subfield code="a">Fuster, Valentin</subfield>
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      <subfield code="a">Lopez-Melgar, Beatriz</subfield>
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      <subfield code="a">Oliva, Belen</subfield>
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      <subfield code="a">Sanchez-Gonzalez, Javier</subfield>
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      <subfield code="a">Macias, Angel</subfield>
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      <subfield code="a">Perez-Asenjo, Braulio</subfield>
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      <subfield code="a">Zamudio, Daniel</subfield>
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      <subfield code="a">Alonso-Farto, Juan C</subfield>
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      <subfield code="a">Espana, Samuel</subfield>
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      <subfield code="a">Mendiguren, Jose M</subfield>
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      <subfield code="a">Bueno, Hector</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Garcia-Ruiz, Jose M</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ibáñez, Borja</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Fernandez-Ortiz, Antonio</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sanz, Javier</subfield>
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      <subfield code="c">2019-04</subfield>
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      <subfield code="a">BACKGROUND: Atherosclerosis is a chronic inflammatory disease, but data on arterial inflammation at early stages is limited. OBJECTIVES: The purpose of this study was to characterize vascular inflammation by hybrid 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography/magnetic resonance imaging (PET/MRI). METHODS: Carotid, aortic, and ilio-femoral 18F-FDG PET/MRI was performed in 755 individuals (age 40 to 54 years; 83.7% men) with known plaques detected by 2-/3-dimensional vascular ultrasound and/or coronary calcification in the PESA (Progression of Early Subclinical Atherosclerosis) study. The authors evaluated the presence, distribution, and number of arterial inflammatory foci (increased 18F-FDG uptake) and plaques with or without inflammation (coincident 18F-FDG uptake). RESULTS: Arterial inflammation was present in 48.2% of individuals (24.4% femorals, 19.3% aorta, 15.8% carotids, and 9.3% iliacs) and plaques in 90.1% (73.9% femorals, 55.8% iliacs, and 53.1% carotids). 18F-FDG arterial uptakes and plaques significantly increased with cardiovascular risk factors (p &lt; 0.01). Coincident 18F-FDG uptakes were present in 287 of 2,605 (11%) plaques, and most uptakes were detected in plaque-free arterial segments (459 of 746; 61.5%). Plaque burden, defined by plaque presence, number, and volume, was significantly higher in individuals with arterial inflammation than in those without (p &lt; 0.01). The number of plaques and 18F-FDG uptakes showed a positive albeit weak correlation (r = 0.25; p &lt; 0.001). CONCLUSIONS: Arterial inflammation is highly prevalent in middle-aged individuals with known subclinical atherosclerosis. Large-scale multiterritorial PET/MRI allows characterization of atherosclerosis-related arterial inflammation and demonstrates 18F-FDG uptake in plaque-free arterial segments and, less frequently, within plaques. These findings suggest an arterial inflammatory state at early stages of atherosclerosis. (Progression of Early Subclinical Atherosclerosis [PESA]; NCT01410318).</subfield>
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      <subfield code="a">J Am Coll Cardiol. 2019; 73(12):1371-1382</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1016/j.jacc.2018.12.075</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">1558-3597</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">0735-1097</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Journal of the American College of Cardiology</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">30922468</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">http://hdl.handle.net/20.500.12105/8351</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">(18)F-FDG PET/MRI</subfield>
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      <subfield code="a">Arterial inflammation</subfield>
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      <subfield code="a">Plaque inflammation</subfield>
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      <subfield code="a">Subclinical atherosclerosis</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Vascular Inflammation in Subclinical Atherosclerosis Detected by Hybrid PET/MRI</subfield>
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