<?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>2026-06-30T04:50:17Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/7211" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/7211</identifier><datestamp>2024-09-27T08:49:38Z</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">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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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Garcia-Ruiz, Jose M</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Mendiguren, Jose M</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Bueno, Hector</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Pocock, Stuart</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ibáñez, Borja</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Fernandez-Ortiz, Antonio</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sanz, Javier</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2017-12-19</subfield>
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      <subfield code="a">BACKGROUND: Absence of cardiovascular risk factors (CVRFs) is traditionally considered low risk for atherosclerosis; however, individuals without CVRFs, as currently defined, still have events. OBJECTIVES: This study sought to identify predictors of subclinical atherosclerosis in CVRF-free individuals. METHODS: Participants from the PESA (Progression of Early Subclinical Atherosclerosis) study (n = 4,184) without conventional CVRFs were evaluated (n = 1,779; 45.0 ± 4.1 years, 50.3% women). CVRF freedom was defined as no current smoking and untreated blood pressure &lt;140/90 mm Hg, fasting glucose &lt;126 mg/dl, total cholesterol &lt;240 mg/dl, low-density lipoprotein cholesterol (LDL-C) &lt;160 mg/dl, and high-density lipoprotein cholesterol ≥40 mg/dl. A subgroup with optimal CVRFs (n = 740) was also defined as having blood pressure &lt;120/80 mm Hg, fasting glucose &lt;100 mg/dl, glycosylated hemoglobin &lt;5.7%, and total cholesterol &lt;200 mg/dl. We evaluated ultrasound-detected carotid, iliofemoral, and abdominal aortic plaques; coronary artery calcification; serum biomarkers; and lifestyle. Adjusted odds ratios (with 95% confidence interval) and ordinal logistic regression models were used. RESULTS: Subclinical atherosclerosis (plaque or coronary artery calcification) was present in 49.7% of CVRF-free participants. Together with male sex and age, LDL-C was independently associated with atherosclerosis presence and extent, in both the CVRF-free and CVRF-optimal groups (odds ratio [×10 mg/dl]: 1.14 to 1.18; p &lt; 0.01 for all). Atherosclerosis presence and extent was also associated in the CVRF-free group with glycosylated hemoglobin levels. CONCLUSIONS: Many CVRF-free middle-aged individuals have atherosclerosis. LDL-C, even at levels currently considered normal, is independently associated with the presence and extent of early systemic atherosclerosis in the absence of major CVRFs. These findings support more effective LDL-C lowering for primordial prevention, even in individuals conventionally considered at optimal risk. (Progression of Early Subclinical Atherosclerosis [PESA] Study; NCT01410318).</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">J Am Coll Cardiol. 2017; 70(24):2979-2991</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1016/j.jacc.2017.10.024</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">29241485</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">http://hdl.handle.net/20.500.12105/7211</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">LDL-cholesterol</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Atherosclerosis</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Risk factors</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Normal LDL-Cholesterol Levels Are Associated With Subclinical Atherosclerosis in the Absence of Risk Factors</subfield>
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