<?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>2026-04-29T04:08:33Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/9946" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/9946</identifier><datestamp>2024-09-27T07:55:22Z</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">Hagensen, Mette K</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Mortensen, Martin B</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Kjolby, Mads</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Palmfeldt, Johan</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Bentzon, Jacob F</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Gregersen, Soeren</subfield>
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      <subfield code="c">2019-07</subfield>
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      <subfield code="a">BACKGROUND AND AIMS: Type 1 diabetes accelerates the development of atherosclerotic cardiovascular diseases. Retention of low-density lipoprotein (LDL) in the arterial wall is a causal step in atherogenesis, but it is unknown whether diabetes alters the propensity of LDL for retention. The present study investigated whether LDL from type 1 diabetic and healthy non-diabetic subjects differed in their ability to bind to the arterial wall in a type 1 diabetic mouse model. METHODS: Fluorescently-labeled LDL obtained from type 1 diabetic patients or healthy controls was injected into mice with type 1 diabetes. The amount of retained LDL in the atherosclerosis-prone inner curvature of the aortic arch was quantified by fluorescence microscopy. Healthy control LDL was in vitro glycated, analyzed for protein glycation by LC-MS/MS, and tested for retention propensity. RESULTS: Retention of LDL from type 1 diabetic patients was 4.35-fold higher compared to LDL from nondiabetic subjects. Nuclear magnetic resonance (NMR) spectroscopy analysis of LDL revealed no differences in the concentration of the atherogenic small dense LDL between type 1 diabetic and non-diabetic subjects. In vitro glycation of LDL from a non-diabetic subject increased retention compared to non-glycated LDL. LC-MS/MS revealed four new glycated spots in the protein sequence of ApoB of in vitro glycated LDL. CONCLUSIONS: LDL from type 1 diabetic patients showed increased retention at atherosclerosis-prone sites in the arterial wall of diabetic mice. Glycation of LDL is one modification that may increase retention, but other, yet unknown, mechanisms are also likely to contribute.</subfield>
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      <subfield code="a">Atherosclerosis. 2019; 286:156-162</subfield>
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      <subfield code="a">0021-9150</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/9946</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">30871723</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1016/j.atherosclerosis.2019.02.027</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">1879-1484</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Atherosclerosis</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Atherosclerosis</subfield>
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      <subfield code="a">Low density lipoprotein</subfield>
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      <subfield code="a">Retention</subfield>
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      <subfield code="a">Type 1 diabetes</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Increased retention of LDL from type 1 diabetic patients in atherosclerosis-prone areas of the murine arterial wall</subfield>
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