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dc.contributor.authorJimenez-Sousa, Maria Angeles
dc.contributor.authorJimenez, Jose Luis
dc.contributor.authorFernandez-Rodriguez, Amanda
dc.contributor.authorBellon, Jose Maria
dc.contributor.authorRodriguez, Carmen
dc.contributor.authorRiera, Melchor
dc.contributor.authorPortilla, Joaquin
dc.contributor.authorCastro Iglesias, Angeles 
dc.contributor.authorMunoz-Fernandez, Maria Angeles
dc.contributor.authorResino, Salvador
dc.date.accessioned2022-01-25T12:15:49Z
dc.date.available2022-01-25T12:15:49Z
dc.date.issued2019
dc.identifier.issn1021-7770
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31640710es
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806573/pdf/12929_2019_Article_577.pdfes
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15901
dc.description.abstractBACKGROUND: Most of the circulating Vitamin D (VitD) is transported bound to vitamin D-binding protein (DBP), and several DBP single nucleotide polymorphisms (SNPs) have been related to circulating VitD concentration and disease. In this study, we evaluated the association among DBP SNPs and AIDS progression in antiretroviral treatment (ART)-naive-HIV-infected patients. METHODS: We performed a retrospective study in 667 patients who were classified according to their pattern of AIDS progression (183 long-term non-progressors (LTNPs), 334 moderate progressors (MPs), and 150 rapid progressors (RPs)) and 113 healthy blood donors (HIV, HCV, and HBV negative subjects). We genotyped seven DBP SNPs (rs16846876, rs12512631, rs2070741, rs2282679, rs7041, rs1155563, rs2298849) using Agena Bioscience's MassARRAY platform. The genetic association was evaluated by Generalized Linear Models adjusted by age at the moment of HIV diagnosis, gender, risk group, and VDR rs2228570 SNP. Multiple testing correction was performed by the false discovery rate (Benjamini and Hochberg procedure; q-value). RESULTS: All SNPs were in HWE (p > 0.05) and had similar genotypic frequencies for DBP SNPs in healthy-controls and HIV-infected patients. In unadjusted GLMs, we only found significant association with AIDS progression in rs16846876 and rs12512631 SNPs. In adjusted GLMs, DBP rs16846876 SNP showed significant association under the recessive inheritance model [LTNPs vs. RPs (adjusted odds ratio (aOR) = 3.53; q-value = 0.044) and LTNPs vs. MPs (aOR = 3.28; q-value = 0.030)] and codominant [LTNPs vs. RPs (aOR = 4.92; q-value = 0.030) and LTNPs vs. MPs (aOR = 3.15; q-value = 0.030)]. Also, we found DBP rs12512631 SNP showed significant association in the inheritance model dominant [LTNPs vs. RPs (aOR = 0.49; q-value = 0.031) and LTNPs vs. MPs (aOR = 0.6; q-value = 0.047)], additive [LTNPs vs. RPs (aOR = 0.61; q-value = 0.031)], overdominant [LTNPs vs. MPs (aOR = 0.55; q-value = 0.032)], and codominant [LTNPs vs. RPs (aOR = 0.52; q-value = 0.036) and LTNPs vs. MPs (aOR = 0.55; q-value = 0.032)]. Additionally, we found a significant association between DBP haplotypes (composed by rs16846876 and rs12512631) and AIDS progression (LTNPs vs RPs): DBP haplotype AC (aOR = 0.63; q-value = 0.028) and the DBP haplotype TT (aOR = 1.64; q-value = 0.028). CONCLUSIONS: DBP rs16846876 and rs12512631 SNPs are related to the patterns of clinical AIDS progression (LTNP, MP, and RP) in ART-naive HIV-infected patients. Our findings provide new knowledge about AIDS progression that may be relevant to understanding the pathogenesis of HIV infection.en
dc.language.isoenges
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshDNA-Binding Proteins*
dc.subject.meshAdult*
dc.subject.meshTranscription Factors*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshAnti-Retroviral Agents*
dc.subject.meshDisease Progression*
dc.subject.meshRetrospective Studies*
dc.subject.meshHIV*
dc.subject.meshCohort Studies*
dc.subject.meshAcquired Immunodeficiency Syndrome*
dc.titleDBP rs16846876 and rs12512631 polymorphisms are associated with progression to AIDS naive HIV-infected patients: a retrospective studyen
dc.typeArtigoes
dc.identifier.doi10.1186/s12929-019-0577-y
dc.identifier.pmid31640710
dc.identifier.sophos32282
dc.issue.number1es
dc.journal.titleJOURNAL OF BIOMEDICAL SCIENCEes
dc.organizationServizo Galego de Saúdees
dc.rights.accessRightsopenAccesses
dc.subject.decsVIH*
dc.subject.decsfactores de transcripción*
dc.subject.decsproteínas de unión al ADN*
dc.subject.decssíndrome de inmunodeficiencia adquirida*
dc.subject.decsestudios retrospectivos*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decsestudios de cohortes*
dc.subject.decsadulto*
dc.subject.decsprogresión de la enfermedad*
dc.subject.decsantirretrovirales*
dc.subject.keywordCHUACes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number26es


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