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                  <mods:namePart>Jimenez-Sousa, Maria Angeles</mods:namePart>
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                  <mods:namePart>Bellón, José María</mods:namePart>
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                  <mods:namePart>Bernal-Morell, Enrique</mods:namePart>
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                  <mods:namePart>Red de Investigación Cooperativa en Investigación en Sida (España)</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2020-01-15T12:51:07Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2019-03-05</mods:dateIssued>
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               <mods:identifier type="citation">J Clin Med. 2019 Mar 5;8(3). pii: E311.</mods:identifier>
               <mods:identifier type="doi">10.3390/jcm8030311</mods:identifier>
               <mods:identifier type="issn">2077-0383</mods:identifier>
               <mods:identifier type="journal">Journal of clinical medicine</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/20.500.13003/17594</mods:identifier>
               <mods:identifier type="pubmedID">30841566</mods:identifier>
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               <mods:abstract>BACKGROUND: Vitamin D is a fundamental regulator of host defenses by activating genes related to innate and adaptive immunity. In this study, we analyzed the association among single nucleotide polymorphisms (SNPs) in the vitamin D receptor (VDR) gene, with clinical patterns of AIDS progression in antiretroviral treatment (ART)-naïve HIV-infected patients. METHODS: We conducted a retrospective study in 667 HIV-infected patients, who were classified within three groups according to their AIDS progression pattern (183 long-term non-progressors (LTNPs), 334 moderate progressors (MPs), and 150 rapid progressors (RPs)). Five VDR SNPs (rs11568820, rs4516035, rs2228570, rs1544410, and rs7975232) were genotyped using Agena Bioscience's MassARRAY platform. RESULTS: Significant association results were found for rs2228570. Within all HIV patients, the presence of T allele at VDR rs2228570 SNP was protective against AIDS progression (ordinal outcome) under additive (adjusted odds ratio (aOR) = 0.75; p = 0.009), dominant (aOR = 0.69; p = 0.015), and codominant (aOR = 0.56; p = 0.017) inheritance models. In addition, the same allele was protective under additive and codominant inheritance models when we compared with LTNPs vs. RPs [aOR = 0.64 (p = 0.019) and aOR = 0.37 (p = 0.018), respectively] and when we compared MPs vs. RPs [aOR = 0.72 (p = 0.035) and aOR = 0.45 (p = 0.028), respectively]. CONCLUSIONS: The VDR rs2228570 T allele was related to a lower AIDS progression pattern in ART-naïve HIV-infected patients. These findings expand upon the knowledge about HIV pathogenesis in untreated HIV-infected patients with different clinical outcomes.</mods:abstract>
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                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:subject>
                  <mods:topic>AIDS</mods:topic>
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               <mods:subject>
                  <mods:topic>LTNPs</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>VDR</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Non-progression</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Single nucleotide polymorphisms</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>VDR rs2228570 Polymorphism Is Related to Non-Progression to AIDS in Antiretroviral Therapy Naïve HIV-Infected Patients</mods:title>
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