Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study

Detalhes bibliográficos
Autor(a) principal: Scalioni, Letícia de Paula
Data de Publicação: 2018
Outros Autores: Santos, Betânia Rodrigues dos, Spritzer, Poli Mara, Villela-Nogueira, Cristiane Alves, Lewis Ximenez, Lia Laura, Pollo-Flores, Priscila, Esberard, Eliane Bordalo Cathalá, Brandão-Mello, Carlos E., Lampe, Elisabeth, Villar, Livia Melo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/174388
Resumo: Potential relationship of vitamin D, vitamin D receptor (VDR), and vitamin D binding protein (DBP) have been suggested in the pathophysiology of hepatitis C virus (HCV) infection. The aim of this observational study is to determine vitamin D levels, and VDR and DBP genetic polymorphism according demographic and laboratory data in chronic HCV patients (CHC). A total of 148 CHC patients gave serum samples for testing 25-hydroxyvitamin D (25 (OH)D) level by immunochemiluminometric assay (<20ng/mL defined as deficient) and donated blood samples to allelic discrimination analysis using TaqMan assays. Analyzed single nucleotide polymorphisms (SNPs) were: VDR-rs7975232 (ApaI) C>A, rs731236 A>G (TaqI), rs1544410 C>T (BsmI), rs10735810 T>C (FokI) and carrier globulin/binding protein (GC)-rs4588 and rs7041 and the haplotype bAt [CCA]. Hepatic fibrosis was assessed using Fib-4 and Forns index. Eighty-two (54.40%) patients demonstrated deficiency of vitamin D and this was associated to AST (P=.019 [CI: 1.003–1.034]), total cholesterol (P=.038 [CI: 1.004–1.164]), fibrosis grade (P<.001 [CI: 0.000–0.844]), and FokI (P=.028) allele T presence. Association was found between VDR polymorphism and fibrosis (BsmI andTaqI), triglycerides (TaqI), and HDL (FokI). DBP polymorphism was associated to HCV genotype (GC rs7041), previous HCV treatment, and GGT (GC rs4588). In conclusion, lowfrequency of vitamin D deficiencywas found, but VDR polymorphisms were frequently associated to fibrosis grade suggesting that they could be used as disease evaluation markers to understand the mechanisms underlying the virus–host interaction.
id UFRGS-2_40eb2e3c2174c0e853e8033179ef3c1a
oai_identifier_str oai:www.lume.ufrgs.br:10183/174388
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Scalioni, Letícia de PaulaSantos, Betânia Rodrigues dosSpritzer, Poli MaraVillela-Nogueira, Cristiane AlvesLewis Ximenez, Lia LauraPollo-Flores, PriscilaEsberard, Eliane Bordalo CathaláBrandão-Mello, Carlos E.Lampe, ElisabethVillar, Livia Melo2018-04-05T02:25:22Z20180025-7974http://hdl.handle.net/10183/174388001063002Potential relationship of vitamin D, vitamin D receptor (VDR), and vitamin D binding protein (DBP) have been suggested in the pathophysiology of hepatitis C virus (HCV) infection. The aim of this observational study is to determine vitamin D levels, and VDR and DBP genetic polymorphism according demographic and laboratory data in chronic HCV patients (CHC). A total of 148 CHC patients gave serum samples for testing 25-hydroxyvitamin D (25 (OH)D) level by immunochemiluminometric assay (<20ng/mL defined as deficient) and donated blood samples to allelic discrimination analysis using TaqMan assays. Analyzed single nucleotide polymorphisms (SNPs) were: VDR-rs7975232 (ApaI) C>A, rs731236 A>G (TaqI), rs1544410 C>T (BsmI), rs10735810 T>C (FokI) and carrier globulin/binding protein (GC)-rs4588 and rs7041 and the haplotype bAt [CCA]. Hepatic fibrosis was assessed using Fib-4 and Forns index. Eighty-two (54.40%) patients demonstrated deficiency of vitamin D and this was associated to AST (P=.019 [CI: 1.003–1.034]), total cholesterol (P=.038 [CI: 1.004–1.164]), fibrosis grade (P<.001 [CI: 0.000–0.844]), and FokI (P=.028) allele T presence. Association was found between VDR polymorphism and fibrosis (BsmI andTaqI), triglycerides (TaqI), and HDL (FokI). DBP polymorphism was associated to HCV genotype (GC rs7041), previous HCV treatment, and GGT (GC rs4588). In conclusion, lowfrequency of vitamin D deficiencywas found, but VDR polymorphisms were frequently associated to fibrosis grade suggesting that they could be used as disease evaluation markers to understand the mechanisms underlying the virus–host interaction.application/pdfengMedicine (Baltimore). Baltimore. Vol. 97, no. 8 (Feb. 2018), e9878 [7] p.FibroseHepatite CPolimorfismo genéticoVitamina DFibrosisHepatitis CPolymorphismVitamin DImpact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional studyEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL001063002.pdf001063002.pdfTexto completo (inglês)application/pdf353966http://www.lume.ufrgs.br/bitstream/10183/174388/1/001063002.pdf1ba80e145962cec1c77daccdede2a623MD51TEXT001063002.pdf.txt001063002.pdf.txtExtracted Texttext/plain39819http://www.lume.ufrgs.br/bitstream/10183/174388/2/001063002.pdf.txt1a03625417f864b26548a63758dfaf61MD52THUMBNAIL001063002.pdf.jpg001063002.pdf.jpgGenerated Thumbnailimage/jpeg2015http://www.lume.ufrgs.br/bitstream/10183/174388/3/001063002.pdf.jpgb5ab6a8a69783149f9587bed60364dd9MD5310183/1743882018-10-25 10:10:21.296oai:www.lume.ufrgs.br:10183/174388Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-10-25T13:10:21Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
title Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
spellingShingle Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
Scalioni, Letícia de Paula
Fibrose
Hepatite C
Polimorfismo genético
Vitamina D
Fibrosis
Hepatitis C
Polymorphism
Vitamin D
title_short Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
title_full Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
title_fullStr Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
title_full_unstemmed Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
title_sort Impact of vitamin D receptor and binding protein gene polymorphisms in clinical and laboratory data of HCV patients : cross sectional study
author Scalioni, Letícia de Paula
author_facet Scalioni, Letícia de Paula
Santos, Betânia Rodrigues dos
Spritzer, Poli Mara
Villela-Nogueira, Cristiane Alves
Lewis Ximenez, Lia Laura
Pollo-Flores, Priscila
Esberard, Eliane Bordalo Cathalá
Brandão-Mello, Carlos E.
Lampe, Elisabeth
Villar, Livia Melo
author_role author
author2 Santos, Betânia Rodrigues dos
Spritzer, Poli Mara
Villela-Nogueira, Cristiane Alves
Lewis Ximenez, Lia Laura
Pollo-Flores, Priscila
Esberard, Eliane Bordalo Cathalá
Brandão-Mello, Carlos E.
Lampe, Elisabeth
Villar, Livia Melo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Scalioni, Letícia de Paula
Santos, Betânia Rodrigues dos
Spritzer, Poli Mara
Villela-Nogueira, Cristiane Alves
Lewis Ximenez, Lia Laura
Pollo-Flores, Priscila
Esberard, Eliane Bordalo Cathalá
Brandão-Mello, Carlos E.
Lampe, Elisabeth
Villar, Livia Melo
dc.subject.por.fl_str_mv Fibrose
Hepatite C
Polimorfismo genético
Vitamina D
topic Fibrose
Hepatite C
Polimorfismo genético
Vitamina D
Fibrosis
Hepatitis C
Polymorphism
Vitamin D
dc.subject.eng.fl_str_mv Fibrosis
Hepatitis C
Polymorphism
Vitamin D
description Potential relationship of vitamin D, vitamin D receptor (VDR), and vitamin D binding protein (DBP) have been suggested in the pathophysiology of hepatitis C virus (HCV) infection. The aim of this observational study is to determine vitamin D levels, and VDR and DBP genetic polymorphism according demographic and laboratory data in chronic HCV patients (CHC). A total of 148 CHC patients gave serum samples for testing 25-hydroxyvitamin D (25 (OH)D) level by immunochemiluminometric assay (<20ng/mL defined as deficient) and donated blood samples to allelic discrimination analysis using TaqMan assays. Analyzed single nucleotide polymorphisms (SNPs) were: VDR-rs7975232 (ApaI) C>A, rs731236 A>G (TaqI), rs1544410 C>T (BsmI), rs10735810 T>C (FokI) and carrier globulin/binding protein (GC)-rs4588 and rs7041 and the haplotype bAt [CCA]. Hepatic fibrosis was assessed using Fib-4 and Forns index. Eighty-two (54.40%) patients demonstrated deficiency of vitamin D and this was associated to AST (P=.019 [CI: 1.003–1.034]), total cholesterol (P=.038 [CI: 1.004–1.164]), fibrosis grade (P<.001 [CI: 0.000–0.844]), and FokI (P=.028) allele T presence. Association was found between VDR polymorphism and fibrosis (BsmI andTaqI), triglycerides (TaqI), and HDL (FokI). DBP polymorphism was associated to HCV genotype (GC rs7041), previous HCV treatment, and GGT (GC rs4588). In conclusion, lowfrequency of vitamin D deficiencywas found, but VDR polymorphisms were frequently associated to fibrosis grade suggesting that they could be used as disease evaluation markers to understand the mechanisms underlying the virus–host interaction.
publishDate 2018
dc.date.accessioned.fl_str_mv 2018-04-05T02:25:22Z
dc.date.issued.fl_str_mv 2018
dc.type.driver.fl_str_mv Estrangeiro
info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/174388
dc.identifier.issn.pt_BR.fl_str_mv 0025-7974
dc.identifier.nrb.pt_BR.fl_str_mv 001063002
identifier_str_mv 0025-7974
001063002
url http://hdl.handle.net/10183/174388
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Medicine (Baltimore). Baltimore. Vol. 97, no. 8 (Feb. 2018), e9878 [7] p.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/174388/1/001063002.pdf
http://www.lume.ufrgs.br/bitstream/10183/174388/2/001063002.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/174388/3/001063002.pdf.jpg
bitstream.checksum.fl_str_mv 1ba80e145962cec1c77daccdede2a623
1a03625417f864b26548a63758dfaf61
b5ab6a8a69783149f9587bed60364dd9
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1801224942205796352