Lower p66Shc promoter methylation in subjects with chronic renal failure

PLoS One. 2021 Sep 16;16(9):e0257176. doi: 10.1371/journal.pone.0257176. eCollection 2021.

Abstract

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.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Case-Control Studies
  • DNA Methylation / genetics*
  • Female
  • Humans
  • Inflammation / genetics
  • Inflammation / pathology
  • Kidney Function Tests
  • Male
  • Malondialdehyde / metabolism
  • Middle Aged
  • Oxidative Stress / genetics
  • Promoter Regions, Genetic*
  • Renal Insufficiency, Chronic / genetics*
  • Renal Insufficiency, Chronic / physiopathology
  • Src Homology 2 Domain-Containing, Transforming Protein 1 / genetics*

Substances

  • SHC1 protein, human
  • Src Homology 2 Domain-Containing, Transforming Protein 1
  • Malondialdehyde

Grants and funding

The author(s) received no specific funding for this work.