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Tumour necrosis factor-related apoptosis-inducing ligand expression in patients with diabetic nephropathy
Wei-Wei Chang1, Wei Liang2, Xin-Ming Yao3
11 Department of Epidemiology and Biostatistics, School of Public Health, Wannan Medical College, China.
Objective:
The objective of this study was to evaluate the expression profile of tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) in patients with diabetic nephropathy (DN).
Methods:
A total of 126 Chinese subjects were enrolled in this study, including 42 patients with diabetes mellitus (DM), 42 patients with DN and 42 healthy controls. Real-time polymerase chain reaction was performed to analyze levels of TRAIL mRNA in peripheral blood mononuclear cells (PBMCs). Serum levels of soluble TRAIL (sTRAIL) and various cytokines were detected with a commercially available enzyme-linked immunosorbent assay kit.
Results:
Compared with the control group, the levels of TRAIL mRNA in PBMCs and sTRAIL in sera were both significantly decreased in the DM and DN patients ( P < 0.05). Conversely, levels of interleukin (IL)-1, IL-6, tumour necrosis factor-α and monocyte chemotactic protein-1 were higher in the DN group than in the control group. Serum levels of TRAIL positively correlated with TRAIL mRNA levels in all of the subjects examined ( P < 0.05).
Conclusions:
These results provide support and a theoretical basis for further research of TRAIL in regard to the pathogenesis of DN.
Insights
Tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) levels were significantly lower in patients with diabetes mellitus and diabetic nephropathy. This finding suggests TRAIL may play a role in diabetic nephropathy pathogenesis.
Area of Science:
- Nephrology
- Immunology
- Endocrinology
Background:
- Diabetic nephropathy (DN) is a major complication of diabetes mellitus.
- Tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) is involved in immune responses and apoptosis.
- The role of TRAIL in DN pathogenesis requires further elucidation.
Purpose of the Study:
- To investigate the expression profile of TRAIL in patients with DN.
- To compare TRAIL levels in patients with diabetes mellitus (DM), DN, and healthy controls.
Main Methods:
- Real-time polymerase chain reaction (PCR) to quantify TRAIL mRNA in peripheral blood mononuclear cells (PBMCs).
- Enzyme-linked immunosorbent assay (ELISA) to measure serum soluble TRAIL (sTRAIL) and cytokine levels.
- Study included 126 Chinese subjects: 42 DM patients, 42 DN patients, and 42 healthy controls.
Main Results:
- TRAIL mRNA and sTRAIL levels were significantly decreased in DM and DN patients compared to controls (P < 0.05).
- DN patients exhibited elevated levels of IL-1, IL-6, TNF-α, and MCP-1 compared to controls.
- Serum TRAIL levels positively correlated with TRAIL mRNA levels across all subjects (P < 0.05).
Conclusions:
- Reduced TRAIL expression is associated with DM and DN.
- Elevated pro-inflammatory cytokines are present in DN patients.
- These findings support further investigation into TRAIL's role in DN pathogenesis.
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