Evaluation of Bach1 mRNA expression in patients with chronic kidney disease: A preliminary study
Denise Mafra1,2,3, Livia Alvarenga1,2,3, Marcia Ribeiro1
1Graduate Program in Biological Sciences - Physiology, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro (RJ), Brazil.
Introduction:
BTB and CNC homology 1 (Bach1) is a protein that antagonizes some actions of nuclear factor erythroid 2-related factor-2 (Nrf2), the master regulator of cytoprotective responses. Bach1 binds to genomic DNA and inhibits the synthesis of antioxidant enzymes, thereby increasing inflammation. Bach1 may be a therapeutic target for mitigating inflammation in chronic kidney disease (CKD) patients. However, no clinical study has been reported on Bach1 in this population. This study aimed to evaluate Bach1 mRNA expression with different treatments for CKD, including conservative treatment (nondialysis), hemodialysis (HD), and peritoneal dialysis (PD).
Methods:
Twenty patients undergoing HD (56.5 [19] years), 15 on PD (54 [24] years) and 13 nondialysis patients (63 [10] years, with an estimated glomerular filtration rate of 41 [14] mL/min/1.73 m2 ) were enrolled in the study. The mRNA expression of Nrf2, NF-kB, heme oxygenase 1 (HO-1), and Bach1 was evaluated in peripheral blood mononuclear cells using quantitative real-time polymerase chain reaction. Malondialdehyde (MDA) was evaluated as a lipid peroxidation marker. Routine biochemical parameters were also evaluated.
Findings:
As expected, patients on dialysis were more inflamed. Bach1 mRNA expression was significantly higher in patients undergoing HD than in PD and nondialysis patients (p < 0.007). The mRNA expression of HO-1, NF-kB, and Nrf2 was not different in the groups.
Conclusion:
In conclusion, CKD patients on HD exhibited an upregulation of Bach1 mRNA expression compared to patients on PD treatment and nondialysis CKD patients. The association between Nrf2 and Bach1 expression in these patients warrants further investigation.
Insights
Chronic kidney disease (CKD) patients on hemodialysis (HD) show higher Bach1 mRNA expression than those on peritoneal dialysis (PD) or conservative treatment. This suggests Bach1 may play a role in inflammation associated with HD in CKD.
Area of Science:
- Biochemistry
- Nephrology
- Molecular Biology
Background:
- BTB and CNC homology 1 (Bach1) antagonizes nuclear factor erythroid 2-related factor-2 (Nrf2), inhibiting antioxidant enzyme synthesis and promoting inflammation.
- Bach1 may be a therapeutic target for managing inflammation in chronic kidney disease (CKD).
- No clinical studies have investigated Bach1 expression in CKD patients undergoing different treatments.
Purpose of the Study:
- To evaluate Bach1 mRNA expression in peripheral blood mononuclear cells of CKD patients.
- To compare Bach1 mRNA levels across different CKD treatment groups: conservative (nondialysis), hemodialysis (HD), and peritoneal dialysis (PD).
Main Methods:
- Quantitative real-time polymerase chain reaction was used to measure mRNA expression of Bach1, Nrf2, NF-kB, and heme oxygenase 1 (HO-1).
- Malondialdehyde (MDA) was assessed as a marker of lipid peroxidation.
- Peripheral blood mononuclear cells were collected from 20 HD patients, 15 PD patients, and 13 nondialysis CKD patients.
Main Results:
- Bach1 mRNA expression was significantly higher in CKD patients undergoing HD compared to those on PD and nondialysis treatment (p < 0.007).
- No significant differences were observed in the mRNA expression of HO-1, NF-kB, or Nrf2 among the treatment groups.
- Dialysis patients generally exhibited higher inflammation levels.
Conclusions:
- CKD patients on hemodialysis demonstrate an upregulation of Bach1 mRNA expression.
- The findings suggest a potential role for Bach1 in the inflammatory processes associated with hemodialysis in CKD.
- Further research is needed to explore the relationship between Nrf2 and Bach1 expression in CKD patients.
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