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Lower p66Shc promoter methylation in subjects with chronic renal failure
OBJECTIVE: To determine the correlation between DNA methylation of p66Shc promoter and some markers of inflammatory and oxidative stress in chronic renal failure (CRF) patients compared with healthy subjects. METHODS: An observational cross-sectional study was conducted in the nephrology department...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445414/ https://www.ncbi.nlm.nih.gov/pubmed/34529688 http://dx.doi.org/10.1371/journal.pone.0257176 |
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author | Hamdi, Radhia Saadallah-Kallel, Amana Ferchichi-Trimeche, Slima Mokdad-Gargouri, Raja Miled, Abdelhedi Benarba, Bachir |
author_facet | Hamdi, Radhia Saadallah-Kallel, Amana Ferchichi-Trimeche, Slima Mokdad-Gargouri, Raja Miled, Abdelhedi Benarba, Bachir |
author_sort | Hamdi, Radhia |
collection | PubMed |
description | OBJECTIVE: To determine the correlation between DNA methylation of p66Shc promoter and some markers of inflammatory and oxidative stress in chronic renal failure (CRF) patients compared with healthy subjects. METHODS: An observational cross-sectional study was conducted in the nephrology department at Sidi Bouzid Regional Hospital (Tunisia). In total, 39 patients with CRF and 37 healthy subjects were included. Several biochemical parameters were measured. Furthermore, markers of the oxidative and inflammatory status (MDA, TAS, SOD, and CRP) were evaluated. The p66Shc methylation status was determined using the methylation-specific PCR. RESULTS: Our results showed that levels of blood glucose, urea, creatinine, uric acid, ChT, TG, albuminuria, CRP and MDA were significantly elevated in CRF patients compared to controls. Furthermore, p66Shc promoter region was highly demethylated in CRF patients compared to healthy controls (84% vs 4%). Our data showed a positive correlation between p66Shc hypomethylation and levels of MDA (r = 0.93; p<0, 05) and CRP (r = 0.89; P <0, 05), as well as a significant negative correlation between p66Shc hypomethylation, TAS (r = -0.76; P <0, 05) and SOD (r = -0.77; p<0, 05) levels. Similarly, there was a positive correlation between p66Shc hypomethylation and the disease stages. Importantly, multiple regression analysis showed that p66shc DNA hypomethylation remains strongly correlated with MDA, CRP and stages of CRF. CONCLUSION: This study indicates that the DNA hypomethylation of p66shc promoter was correlated with oxidative and inflammatory stress and the disease stages in CRF patients. |
format | Online Article Text |
id | pubmed-8445414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84454142021-09-17 Lower p66Shc promoter methylation in subjects with chronic renal failure Hamdi, Radhia Saadallah-Kallel, Amana Ferchichi-Trimeche, Slima Mokdad-Gargouri, Raja Miled, Abdelhedi Benarba, Bachir PLoS One Research Article OBJECTIVE: To determine the correlation between DNA methylation of p66Shc promoter and some markers of inflammatory and oxidative stress in chronic renal failure (CRF) patients compared with healthy subjects. METHODS: An observational cross-sectional study was conducted in the nephrology department at Sidi Bouzid Regional Hospital (Tunisia). In total, 39 patients with CRF and 37 healthy subjects were included. Several biochemical parameters were measured. Furthermore, markers of the oxidative and inflammatory status (MDA, TAS, SOD, and CRP) were evaluated. The p66Shc methylation status was determined using the methylation-specific PCR. RESULTS: Our results showed that levels of blood glucose, urea, creatinine, uric acid, ChT, TG, albuminuria, CRP and MDA were significantly elevated in CRF patients compared to controls. Furthermore, p66Shc promoter region was highly demethylated in CRF patients compared to healthy controls (84% vs 4%). Our data showed a positive correlation between p66Shc hypomethylation and levels of MDA (r = 0.93; p<0, 05) and CRP (r = 0.89; P <0, 05), as well as a significant negative correlation between p66Shc hypomethylation, TAS (r = -0.76; P <0, 05) and SOD (r = -0.77; p<0, 05) levels. Similarly, there was a positive correlation between p66Shc hypomethylation and the disease stages. Importantly, multiple regression analysis showed that p66shc DNA hypomethylation remains strongly correlated with MDA, CRP and stages of CRF. CONCLUSION: This study indicates that the DNA hypomethylation of p66shc promoter was correlated with oxidative and inflammatory stress and the disease stages in CRF patients. Public Library of Science 2021-09-16 /pmc/articles/PMC8445414/ /pubmed/34529688 http://dx.doi.org/10.1371/journal.pone.0257176 Text en © 2021 Hamdi et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hamdi, Radhia Saadallah-Kallel, Amana Ferchichi-Trimeche, Slima Mokdad-Gargouri, Raja Miled, Abdelhedi Benarba, Bachir Lower p66Shc promoter methylation in subjects with chronic renal failure |
title | Lower p66Shc promoter methylation in subjects with chronic renal failure |
title_full | Lower p66Shc promoter methylation in subjects with chronic renal failure |
title_fullStr | Lower p66Shc promoter methylation in subjects with chronic renal failure |
title_full_unstemmed | Lower p66Shc promoter methylation in subjects with chronic renal failure |
title_short | Lower p66Shc promoter methylation in subjects with chronic renal failure |
title_sort | lower p66shc promoter methylation in subjects with chronic renal failure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445414/ https://www.ncbi.nlm.nih.gov/pubmed/34529688 http://dx.doi.org/10.1371/journal.pone.0257176 |
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