<?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>2026-07-24T06:25:06Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/7200" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/7200</identifier><datestamp>2025-04-03T17:28:37Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_15322</setSpec><setSpec>col_20.500.12105_19609</setSpec><setSpec>col_20.500.12105_16978</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">Medrano, Luz Maria</subfield>
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      <subfield code="a">Berenguer, Juan</subfield>
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      <subfield code="a">Jimenez-Sousa, Maria Angeles</subfield>
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      <subfield code="a">Aldámiz-Echevarria, Teresa</subfield>
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      <subfield code="a">Tejerina, Francisco</subfield>
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      <subfield code="a">Díez, Cristina</subfield>
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      <subfield code="a">Vigon-Hernandez, Lorena</subfield>
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      <subfield code="a">Fernandez-Rodriguez, Amanda</subfield>
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      <subfield code="a">Resino, Salvador</subfield>
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      <subfield code="c">2017-10-10</subfield>
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      <subfield code="a">The adenosine deaminase acting on RNA (ADAR1) gene is an interferon-stimulated gene involved in liver injury protection. Our aim was to analyze the association of polymorphisms within this gene with the severity of liver disease in European HIV/HCV-coinfected patients. We performed a cross-sectional study in 220 patients that underwent a liver biopsy. Five SNPs in the ADAR1 gene (rs1127326, rs1127317, rs1127314, rs1127313, rs2229857) were genotyped by GoldenGate assay. The outcome variables were fibrosis stage and necroinflammatory activity grade by METAVIR-score, aspartate aminotransferase to platelet ratio index (APRI), FIB-4 index, and fibrosis progression rate (FPR). In multivariate analysis, fibrosis progression rate (FPR) (aAMRs = 0.97) decreased in a dose-dependent manner with the presence of rs2229857_T, rs1127313_G, rs1127314_G and rs1127317_G; while rs1127326_T allele had only significant associations with FIB-4 (aAMRs ≤ 0.63) and FPR (aAMRs ≤ 0.97). Moreover, carriers of rs2229857_T, rs1127314_G, rs1127317_G, and rs1127326_T alleles were protected against advanced fibrosis (F ≥ 3) (adjusted ORs (aORs) ≤ 0.44), APRI ≥ 1.5 (aORs ≤ 0.33), and FPR ≥ 0.075 (aORs ≤ 0.45). rs1127313_G carriers showed lower odds of having F ≥ 3 (aORs = 0.39), FIB4 ≥ 3.25 (aOR = 0.22) and FPR ≥ 0.075 (aORs = 0.44). In conclusion, ADAR1 polymorphisms protected against severe liver disease in HIV/HCV-coinfected patients. These results could be used to improve therapeutic decision-making in clinical practice.</subfield>
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      <subfield code="a">Sci Rep. 2017 Oct 10;7(1):12918.</subfield>
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      <subfield code="a">10.1038/s41598-017-12885-4</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">29018269</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/7200</subfield>
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      <subfield code="a">ADAR1 polymorphisms are related to severity of liver fibrosis in HIV/HCV-coinfected patients</subfield>
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