<?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>2026-05-21T23:07:17Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/18134" metadataPrefix="mets">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><mets xmlns="http://www.loc.gov/METS/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.12105-18134" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.12105/18134">
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                  <mods:namePart>García-Marchena, Nuria</mods:namePart>
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                  <mods:namePart>Pizarro, Nieves</mods:namePart>
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                  <mods:namePart>Pavón, Francisco-Javier</mods:namePart>
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                  <mods:namePart>Martínez-Huélamo, Miriam</mods:namePart>
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                  <mods:namePart>Flores-López, María</mods:namePart>
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                  <mods:namePart>Requena-Ocaña, Nerea</mods:namePart>
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                  <mods:namePart>Araos, Pedro</mods:namePart>
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                  <mods:namePart>Silva-Peña, Daniel</mods:namePart>
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                  <mods:namePart>Suárez, Juan</mods:namePart>
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                  <mods:namePart>Santín, Luis J</mods:namePart>
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                  <mods:namePart>de la Torre, Rafael</mods:namePart>
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                  <mods:namePart>Rodríguez de Fonseca, Fernando</mods:namePart>
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                  <mods:namePart>Serrano, Antonia</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-12T19:47:36Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2020-10-13</mods:dateIssued>
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               <mods:identifier type="doi">10.1038/s41598-020-74155-0</mods:identifier>
               <mods:identifier type="e-issn">2045-2322</mods:identifier>
               <mods:identifier type="journal">Scientific reports</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/10668/16413</mods:identifier>
               <mods:identifier type="pubmedID">33051508</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/18134</mods:identifier>
               <mods:abstract>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.</mods:abstract>
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                  <mods:title>Potential association of plasma lysophosphatidic acid (LPA) species with cognitive impairment in abstinent alcohol use disorders outpatients.</mods:title>
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