<?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>2026-08-29T14:07:33Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/7065" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/7065</identifier><datestamp>2024-09-27T16:17:13Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19608</setSpec><setSpec>col_20.500.12105_19609</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">dc</subfield>
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      <subfield code="a">Jimenez-Sousa, Maria Angeles</subfield>
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      <subfield code="a">López, Elisabeth</subfield>
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      <subfield code="a">Fernandez-Rodriguez, Amanda</subfield>
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      <subfield code="a">Tamayo, Eduardo</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Fernandez-Navarro, Pablo L</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Segura-Roda, Laura</subfield>
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      <subfield code="a">Heredia, María</subfield>
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      <subfield code="a">Gómez-Herreras, José I</subfield>
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      <subfield code="a">Bustamante, Jesús</subfield>
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      <subfield code="a">García-Gómez, Juan Miguel</subfield>
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      <subfield code="a">Bermejo-Martin, Jesús F</subfield>
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      <subfield code="a">Resino, Salvador</subfield>
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      <subfield code="c">2012-07-20</subfield>
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      <subfield code="a">BACKGROUND: Chronic kidney disease progression has been linked to pro-inflammatory cytokines and markers of inflammation. These markers are also elevated in end-stage renal disease (ESRD), which constitutes a serious public health problem. OBJECTIVE: To investigate whether single nucleotide polymorphisms (SNPs) located in genes related to immune and inflammatory processes, could be associated with ESRD development. DESIGN AND METHODS: A retrospective case-control study was carried out on 276 patients with ESRD and 288 control subjects. Forty-eight SNPs were genotyped via SNPlex platform. Logistic regression was used to assess the relationship between each sigle polymorphism and the development of ESRD. RESULTS: Four polymorphisms showed association with ESRD: rs1801275 in the interleukin 4 receptor (IL4R) gene (OR: 0.66 (95%CI = 0.46-0.95); p = 0.025; overdominant model), rs4586 in chemokine (C-C motif) ligand 2 (CCL2) gene (OR: 0.70 (95%CI = 0.54-0.90); p = 0.005; additive model), rs301640 located in an intergenic binding site for signal transducer and activator of transcription 4 (STAT4) (OR: 1.82 (95%CI = 1.17-2.83); p = 0.006; additive model) and rs7830 in the nitric oxide synthase 3 (NOS3) gene (OR: 1.31 (95%CI = 1.01-1.71); p = 0.043; additive model). After adjusting for multiple testing, results lost significance. CONCLUSION: Our preliminary data suggest that four genetic polymorphisms located in genes related to inflammation and immune processes could help to predict the risk of developing ESRD.</subfield>
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      <subfield code="a">BMC Med Genet. 2012 Jul 20;13:58.</subfield>
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      <subfield code="a">10.1186/1471-2350-13-58</subfield>
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      <subfield code="a">1471-2350</subfield>
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      <subfield code="a">BMC medical genetics</subfield>
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      <subfield code="a">22817530</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/7065</subfield>
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      <subfield code="a">Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study</subfield>
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