<?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>2026-06-14T03:29:51Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/8352" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/8352</identifier><datestamp>2024-09-27T08:46:39Z</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">Fernandez-Friera, Leticia</subfield>
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      <subfield code="a">Peñalvo, Jose L</subfield>
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      <subfield code="a">Fernandez-Ortiz, Antonio</subfield>
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      <subfield code="a">Ibáñez, Borja</subfield>
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      <subfield code="a">Lopez-Melgar, Beatriz</subfield>
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      <subfield code="a">Laclaustra, Martin</subfield>
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      <subfield code="a">Mocoroa, Agustín</subfield>
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      <subfield code="a">Mendiguren, Jose M</subfield>
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      <subfield code="a">Martínez de Vega, Vicente</subfield>
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      <subfield code="a">Garcia, Laura</subfield>
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      <subfield code="a">Molina, Jesus</subfield>
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      <subfield code="a">Sanchez-Gonzalez, Javier</subfield>
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      <subfield code="a">Guzman-Martinez, Gabriela</subfield>
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      <subfield code="a">Alonso-Farto, Juan C</subfield>
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      <subfield code="a">Guallar, Eliseo</subfield>
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      <subfield code="a">Civeira, Fernando</subfield>
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      <subfield code="a">Sillesen, Henrik</subfield>
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      <subfield code="a">Pocock, Stuart</subfield>
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      <subfield code="a">Ordovas, Jose M</subfield>
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      <subfield code="a">Sanz, Gines</subfield>
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      <subfield code="a">Jimenez-Borreguero, Luis J.</subfield>
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      <subfield code="a">Fuster, Valentin</subfield>
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      <subfield code="c">2015-06-16</subfield>
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      <subfield code="a">BACKGROUND: Data are limited on the presence, distribution, and extent of subclinical atherosclerosis in middle-aged populations. METHODS AND RESULTS: The PESA (Progression of Early Subclinical Atherosclerosis) study prospectively enrolled 4184 asymptomatic participants 40 to 54 years of age (mean age, 45.8 years; 63% male) to evaluate the systemic extent of atherosclerosis in the carotid, abdominal aortic, and iliofemoral territories by 2-/3-dimensional ultrasound and coronary artery calcification by computed tomography. The extent of subclinical atherosclerosis, defined as presence of plaque or coronary artery calcification ≥1, was classified as focal (1 site affected), intermediate (2-3 sites), or generalized (4-6 sites) after exploration of each vascular site (right/left carotids, aorta, right/left iliofemorals, and coronary arteries). Subclinical atherosclerosis was present in 63% of participants (71% of men, 48% of women). Intermediate and generalized atherosclerosis was identified in 41%. Plaques were most common in the iliofemorals (44%), followed by the carotids (31%) and aorta (25%), whereas coronary artery calcification was present in 18%. Among participants with low Framingham Heart Study (FHS) 10-year risk, subclinical disease was detected in 58%, with intermediate or generalized disease in 36%. When longer-term risk was assessed (30-year FHS), 83% of participants at high risk had atherosclerosis, with 66% classified as intermediate or generalized. CONCLUSIONS: Subclinical atherosclerosis was highly prevalent in this middle-aged cohort, with nearly half of the participants classified as having intermediate or generalized disease. Most participants at high FHS risk had subclinical disease; however, extensive atherosclerosis was also present in a substantial number of low-risk individuals, suggesting added value of imaging for diagnosis and prevention. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01410318.</subfield>
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      <subfield code="a">Circulation. 2015; 131(24):2104-13</subfield>
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      <subfield code="a">10.1161/CIRCULATIONAHA.114.014310</subfield>
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      <subfield code="a">1524-4539</subfield>
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      <subfield code="a">0009-7322</subfield>
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      <subfield code="a">Circulation</subfield>
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      <subfield code="a">25882487</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/8352</subfield>
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      <subfield code="a">Atherosclerosis</subfield>
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      <subfield code="a">Epidemiology</subfield>
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      <subfield code="a">Multidetector computed tomography</subfield>
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      <subfield code="a">Risk assessment</subfield>
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      <subfield code="a">Ultrasonography</subfield>
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      <subfield code="a">Prevalence, Vascular Distribution, and Multiterritorial Extent of Subclinical Atherosclerosis in a Middle-Aged Cohort: The PESA (Progression of Early Subclinical Atherosclerosis) Study</subfield>
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