<?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>2026-07-22T11:08:56Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18134" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/18134</identifier><datestamp>2024-09-21T23:29:17Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec><setSpec>col_20.500.12105_16971</setSpec><setSpec>col_20.500.12105_16983</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">García-Marchena, Nuria</subfield>
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      <subfield code="a">Pizarro, Nieves</subfield>
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      <subfield code="a">Pavón, Francisco-Javier</subfield>
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      <subfield code="a">Martínez-Huélamo, Miriam</subfield>
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      <subfield code="a">Flores-López, María</subfield>
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      <subfield code="a">Requena-Ocaña, Nerea</subfield>
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      <subfield code="a">Araos, Pedro</subfield>
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      <subfield code="a">Silva-Peña, Daniel</subfield>
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      <subfield code="a">Suárez, Juan</subfield>
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      <subfield code="a">Santín, Luis J</subfield>
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      <subfield code="a">de la Torre, Rafael</subfield>
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      <subfield code="a">Rodríguez de Fonseca, Fernando</subfield>
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      <subfield code="a">Serrano, Antonia</subfield>
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      <subfield code="c">2020-10-13</subfield>
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      <subfield code="a">Lysophosphatidic acid (LPA) species are bioactive lipids participating in neurodevelopmental processes. The aim was to investigate whether the relevant species of LPA were associated with clinical features of alcohol addiction. A total of 55 abstinent alcohol use disorder (AUD) patients were compared with 34 age/sex/body mass index-matched controls. Concentrations of total LPA and 16:0-LPA, 18:0-LPA, 18:1-LPA, 18:2-LPA and 20:4-LPA species were quantified and correlated with neuroplasticity-associated growth factors including brain derived neurotrophic factor (BDNF), insulin-like growth factor-1 (IGF-1) and IGF-2, and neurotrophin-3 (NT-3). AUD patients showed dysexecutive syndrome (22.4%) and memory impairment (32.6%). Total LPA, 16:0-LPA, 18:0-LPA and 18:1-LPA concentrations, were decreased in the AUD group compared to control group. Total LPA, 16:0-LPA, 18:2-LPA and 20:4-LPA concentrations were decreased in men compared to women. Frontal lobe functions correlated with plasma LPA species. Alcohol-cognitive impairments could be related with the deregulation of the LPA species, especially in 16:0-LPA, 18:1-LPA and 20:4-LPA. Concentrations of BDNF correlated with total LPA, 18:2-LPA and 20:4-LPA species. The relation between LPA species and BDNF is interesting in plasticity and neurogenesis functions, their involvement in AUD might serve as a biomarker of cognitive impairment.</subfield>
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      <subfield code="a">10.1038/s41598-020-74155-0</subfield>
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      <subfield code="a">2045-2322</subfield>
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      <subfield code="a">Scientific reports</subfield>
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      <subfield code="a">http://hdl.handle.net/10668/16413</subfield>
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      <subfield code="a">33051508</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/18134</subfield>
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      <subfield code="a">Potential association of plasma lysophosphatidic acid (LPA) species with cognitive impairment in abstinent alcohol use disorders outpatients.</subfield>
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