Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.

To explore the mechanisms underlying the suggested role of the vitamin D/vitamin D receptor (VDR) complex in the pathogenesis of obesity we performed genetic and immunologic analyses in obese and non-obese Saudi individuals without other concomitant chronic diseases. Genomic DNA was genotyped for ge...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Nasser M Al-Daghri, Franca R Guerini, Omar S Al-Attas, Majed S Alokail, Khalid M Alkharfy, Hossam M Draz, Cristina Agliardi, Andrea S Costa, Irma Saulle, Abdul Khader Mohammed, Mara Biasin, Mario Clerici
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2014
Materias:
R
Q
Acceso en línea:https://doaj.org/article/da0bf813d14548d0a519aaf44564dc0b
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:da0bf813d14548d0a519aaf44564dc0b
record_format dspace
spelling oai:doaj.org-article:da0bf813d14548d0a519aaf44564dc0b2021-11-25T06:08:34ZVitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.1932-620310.1371/journal.pone.0102141https://doaj.org/article/da0bf813d14548d0a519aaf44564dc0b2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25020064/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203To explore the mechanisms underlying the suggested role of the vitamin D/vitamin D receptor (VDR) complex in the pathogenesis of obesity we performed genetic and immunologic analyses in obese and non-obese Saudi individuals without other concomitant chronic diseases. Genomic DNA was genotyped for gene single nucleotide polymorphisms (SNPs) of VDR by allelic discrimination in 402 obese (body mass index -BMI≥30 kg/m2) and 489 non-obese (BMI<30 kg/m2) Saudis. Q-PCR analyses were performed using an ABI Prism 7000 Sequence Detection System. The inflammosome pathway was analysed by PCR, cytokines and plasma lipopolysaccaride (LPS) concentrations with ELISA assays. Results showed that the VDR SNPs rs731236 (G) (TaqI) and rs1544410 (T) (Bsm-I) minor allele polymorphisms are significantly more frequent in obese individuals (p = 0.009, β = 0.086 and p = 0.028, β = 0.072, respectively). VDR haplotypes identified are positively (GTA) (p = 0.008, β = 1.560); or negatively (ACC) (p = 0.044, β = 0.766) associated with obesity and higher BMI scores. The GTA "risk" haplotype was characterized by an up-regulation of inflammosome components, a higher production of proinflammatory cytokines (p<0.05) and a lower VDR expression. Plasma LPS concentration was also increased in GTA obese individuals (p<0.05), suggesting an alteration of gut permeability leading to microbial translocation. Data herein indicate that polymorphisms affecting the vitamin D/VDR axis play a role in obesity that is associated with an ongoing degree of inflammation, possibly resulting from alterations of gut permeability and microbial translocation. These results could help the definition of VDR fingerprints that predict an increased risk of developing obesity and might contribute to the identification of novel therapeutic strategies for this metabolic condition.Nasser M Al-DaghriFranca R GueriniOmar S Al-AttasMajed S AlokailKhalid M AlkharfyHossam M DrazCristina AgliardiAndrea S CostaIrma SaulleAbdul Khader MohammedMara BiasinMario ClericiPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 7, p e102141 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Nasser M Al-Daghri
Franca R Guerini
Omar S Al-Attas
Majed S Alokail
Khalid M Alkharfy
Hossam M Draz
Cristina Agliardi
Andrea S Costa
Irma Saulle
Abdul Khader Mohammed
Mara Biasin
Mario Clerici
Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
description To explore the mechanisms underlying the suggested role of the vitamin D/vitamin D receptor (VDR) complex in the pathogenesis of obesity we performed genetic and immunologic analyses in obese and non-obese Saudi individuals without other concomitant chronic diseases. Genomic DNA was genotyped for gene single nucleotide polymorphisms (SNPs) of VDR by allelic discrimination in 402 obese (body mass index -BMI≥30 kg/m2) and 489 non-obese (BMI<30 kg/m2) Saudis. Q-PCR analyses were performed using an ABI Prism 7000 Sequence Detection System. The inflammosome pathway was analysed by PCR, cytokines and plasma lipopolysaccaride (LPS) concentrations with ELISA assays. Results showed that the VDR SNPs rs731236 (G) (TaqI) and rs1544410 (T) (Bsm-I) minor allele polymorphisms are significantly more frequent in obese individuals (p = 0.009, β = 0.086 and p = 0.028, β = 0.072, respectively). VDR haplotypes identified are positively (GTA) (p = 0.008, β = 1.560); or negatively (ACC) (p = 0.044, β = 0.766) associated with obesity and higher BMI scores. The GTA "risk" haplotype was characterized by an up-regulation of inflammosome components, a higher production of proinflammatory cytokines (p<0.05) and a lower VDR expression. Plasma LPS concentration was also increased in GTA obese individuals (p<0.05), suggesting an alteration of gut permeability leading to microbial translocation. Data herein indicate that polymorphisms affecting the vitamin D/VDR axis play a role in obesity that is associated with an ongoing degree of inflammation, possibly resulting from alterations of gut permeability and microbial translocation. These results could help the definition of VDR fingerprints that predict an increased risk of developing obesity and might contribute to the identification of novel therapeutic strategies for this metabolic condition.
format article
author Nasser M Al-Daghri
Franca R Guerini
Omar S Al-Attas
Majed S Alokail
Khalid M Alkharfy
Hossam M Draz
Cristina Agliardi
Andrea S Costa
Irma Saulle
Abdul Khader Mohammed
Mara Biasin
Mario Clerici
author_facet Nasser M Al-Daghri
Franca R Guerini
Omar S Al-Attas
Majed S Alokail
Khalid M Alkharfy
Hossam M Draz
Cristina Agliardi
Andrea S Costa
Irma Saulle
Abdul Khader Mohammed
Mara Biasin
Mario Clerici
author_sort Nasser M Al-Daghri
title Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
title_short Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
title_full Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
title_fullStr Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
title_full_unstemmed Vitamin D receptor gene polymorphisms are associated with obesity and inflammosome activity.
title_sort vitamin d receptor gene polymorphisms are associated with obesity and inflammosome activity.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/da0bf813d14548d0a519aaf44564dc0b
work_keys_str_mv AT nassermaldaghri vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT francarguerini vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT omarsalattas vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT majedsalokail vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT khalidmalkharfy vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT hossammdraz vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT cristinaagliardi vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT andreascosta vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT irmasaulle vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT abdulkhadermohammed vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT marabiasin vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
AT marioclerici vitamindreceptorgenepolymorphismsareassociatedwithobesityandinflammosomeactivity
_version_ 1718414133131476992