<?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>2026-05-22T17:28:03Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/7260" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/7260</identifier><datestamp>2024-09-27T08:04:41Z</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">Zanon-Moreno, Vicente</subfield>
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      <subfield code="a">Ortega-Azorin, Carolina</subfield>
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      <subfield code="a">Asensio-Marquez, Eva M</subfield>
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      <subfield code="a">Garcia-Medina, Jose J</subfield>
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      <subfield code="a">Pinazo-Duran, Maria D</subfield>
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      <subfield code="a">Coltell, Oscar</subfield>
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      <subfield code="a">Ordovas, Jose M</subfield>
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      <subfield code="a">Corella, Dolores</subfield>
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      <subfield code="c">2017-11-01</subfield>
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      <subfield code="a">Primary open-angle glaucoma (POAG) is a leading cause of blindness worldwide. The genetics of POAG are complex, and population-specific effects have been reported. Although many polymorphisms associated with POAG risk have been reported, few studies have analyzed their additive effects. We investigated, in a southern European Mediterranean population, the association between relevant POAG polymorphisms, identified by initial genome-wide association studies (GWASs) and POAG risk, both separately and as an aggregated multi-locus genetic risk score (GRS). Also, bearing in mind that oxidative stress is a factor increasingly recognized in the pathogenesis of POAG, we analyzed the potential association of the GRS with plasma concentrations of antioxidant vitamins (C and E). We carried out a case-control study including 391 POAG cases and 383 healthy controls, and analyzed four genetic polymorphisms (rs4656461-TMCO1, rs4236601-CAV1/CAV2, rs2157719-CDKN2B-AS1 and rs3088440-CDKN2A). An unweighted GRS including the four non-linked polymorphisms was constructed. A strong association between the GRS and POAG risk was found. When three categories of the GRS were considered, subjects in the top category of the GRS were 2.92 (95% confidence interval (CI): 1.79-4.77) times more likely to have POAG compared with participants in the bottom category (p &lt; 0.001). Moreover, the GRS was inversely correlated with plasma vitamin C (p = 0.002) and vitamin E (p = 0.001) concentrations, even after additional adjustment for POAG status. In conclusion, we have found a strong association between the GRS and POAG risk in this Mediterranean population. While the additional correlation found between GRS and low levels of vitamins C and E does not indicated a causal relationship, it does suggest the need for new and deeper research into the effects of oxidative stress as a potential mechanism for those associations.</subfield>
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      <subfield code="a">Int J Mol Sci. 2017; 18(11):E2302</subfield>
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      <subfield code="a">10.3390/ijms18112302</subfield>
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      <subfield code="a">1422-0067</subfield>
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      <subfield code="a">1422-0067</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">International journal of molecular sciences</subfield>
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      <subfield code="a">29104244</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/7260</subfield>
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      <subfield code="a">GWAS</subfield>
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      <subfield code="a">Genetic risk score</subfield>
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      <subfield code="a">Genetics</subfield>
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      <subfield code="a">Nutrition</subfield>
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      <subfield code="a">Primary open-angle glaucoma</subfield>
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      <subfield code="a">Vitamin C</subfield>
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      <subfield code="a">Vitamin E</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations</subfield>
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