<?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>2026-04-17T18:42:01Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/16709" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/16709</identifier><datestamp>2024-09-27T08:45:37Z</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">Devesa, Ana</subfield>
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      <subfield code="a">Fuster, Valentin</subfield>
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      <subfield code="a">Vazirani, Ravi</subfield>
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      <subfield code="a">Garcia-Lunar, Ines</subfield>
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      <subfield code="a">Oliva, Belen</subfield>
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      <subfield code="a">Espana, Samuel</subfield>
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      <subfield code="a">Moreno-Arciniegas, Andrea</subfield>
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      <subfield code="a">Sanz, Javier</subfield>
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      <subfield code="a">Perez-Herreras, Cristina</subfield>
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      <subfield code="a">Bueno, Hector</subfield>
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      <subfield code="a">Lara-Pezzi, Enrique</subfield>
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      <subfield code="a">Garcia-Alvarez, Ana</subfield>
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      <subfield code="a">de Vega, Vicente Martínez</subfield>
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      <subfield code="a">Fernandez-Friera, Leticia</subfield>
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      <subfield code="a">Trivieri, Maria G</subfield>
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      <subfield code="a">Fernandez-Ortiz, Antonio</subfield>
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      <subfield code="a">Rossello, Xavier</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Sanchez-Gonzalez, Javier</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ibáñez, Borja</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2023-11-01</subfield>
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      <subfield code="a">OBJECTIVE&#xd;
Experimental evidence suggests that metabolic syndrome (MetS) is associated with changes in cardiac metabolism. Whether this association occurs in humans is unknown.&#xd;
RESEARCH DESIGN AND METHODS&#xd;
821 asymptomatic individuals from the Progression of Early Subclinical Atherosclerosis (PESA) study (50.6 [46.9-53.6] years, 83.7% male) underwent two whole-body 18F-fluorodeoxyglucose positron emission tomography-magnetic resonance (18F-FDG PET-MR) 4.8 ± 0.6 years apart. Presence of myocardial 18F-FDG uptake was evaluated qualitatively and quantitatively. No myocardial uptake was grade 0, while positive uptake was classified in grades 1-3 according to target-to-background ratio tertiles.&#xd;
RESULTS&#xd;
One hundred fifty-six participants (19.0%) showed no myocardial 18F-FDG uptake, and this was significantly associated with higher prevalence of MetS (29.0% vs. 13.9%, P &lt; 0.001), hypertension (29.0% vs. 18.0%, P = 0.002), and diabetes (11.0% vs. 3.2%, P &lt; 0.001), and with higher insulin resistance index (HOMA-IR, 1.64% vs. 1.23%, P &lt; 0.001). Absence of myocardial uptake was associated with higher prevalence of early atherosclerosis (i.e., arterial 18F-FDG uptake, P = 0.004). On follow-up, the associations between myocardial 18F-FDG uptake and risk factors were replicated, and MetS was more frequent in the group without myocardial uptake. The increase in HOMA-IR was associated with a progressive decrease in myocardial uptake (P &lt; 0.001). In 82% of subjects, the categorization according to presence/absence of myocardial 18F-FDG uptake did not change between baseline and follow-up. MetS regression on follow-up was associated with a significant (P &lt; 0.001) increase in myocardial uptake.&#xd;
CONCLUSIONS&#xd;
Apparently healthy individuals without cardiac 18F-FDG uptake have higher HOMA-IR and higher prevalence of MetS traits, cardiovascular risk factors, and early atherosclerosis. An improvement in cardiometabolic profile is associated with the recovery of myocardial 18F-FDG uptake at follow-up.</subfield>
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      <subfield code="a">Diabetes Care. 2023 Nov 1;46(11):2050-2057.</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/16709</subfield>
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      <subfield code="a">37713581</subfield>
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      <subfield code="a">10.2337/dc23-0871</subfield>
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      <subfield code="a">1935-5548</subfield>
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      <subfield code="a">Diabetes care</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Cardiac Insulin Resistance in Subjects With Metabolic Syndrome Traits and Early Subclinical Atherosclerosis.</subfield>
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