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[Elevated plasma homocysteine and glutathione level in patients with renal failure]
Insights
Homocysteine (Hcy) levels increase with chronic kidney disease (CKD) progression, particularly in hemodialysis patients. Glutathione (Glt) levels decrease in dialysis patients, showing complex interactions with Hcy and kidney function.
Area of Science:
- Biochemistry
- Nephrology
- Clinical Chemistry
Context:
- Chronic kidney disease (CKD) affects numerous patients globally.
- Biochemical markers like homocysteine (Hcy) and glutathione (Glt) play crucial roles in metabolic processes.
- Understanding these markers' behavior in CKD is vital for patient management.
Purpose:
- To investigate plasma levels of homocysteine (Hcy) and glutathione (Glt) in patients with varying stages of chronic kidney disease (CKD).
- To analyze the relationship between Hcy and Glt levels and the severity of kidney dysfunction, including glomerular filtration rate (GFR).
- To compare these biochemical markers between predialysis and hemodialysis patient groups.
Summary:
- Elevated plasma homocysteine (Hcy) was observed even in early stages of CKD, escalating significantly in hemodialysis patients.
- Total and reduced Hcy (tHcy, rHcy) levels were higher in CKD patients, with a greater proportion of rHcy compared to healthy subjects.
- A negative correlation between GFR and Hcy was found in predialysis patients. Glutathione (Glt) levels were lower in dialysis patients than predialysis patients, with a direct dependence on tHcy in the predialysis group.
Impact:
- Findings highlight Hcy as a potential biomarker for CKD progression and severity.
- The study provides insights into the altered redox balance in CKD patients.
- Results may inform future therapeutic strategies targeting Hcy and Glt metabolism in kidney disease.
Abstract:
The levels of homocysteine (Hcy) and glutatione (Glt) were determined in plasma of 219 patients with different stages of chronic kidney disease (CKD) (94 patients received chronic bicarbonate hemodialysis and 125 patients were at predialysis stage). The elevated Hcy level was detected in an early stage of CKD and reached maximal values and spreading in the hemodialysis patients. The levels of total and reduced Hcy (tHcy and rHcy, respectively) were also higher in CKD patients: the proportion of rHcy in total pool of plasma Hcy was significally higher than in healthy subjects. In the group of non-dialysed patients the reverse dependance between glomerular filtration rate (GFR) value and Hcy plasma concentration was found. We did not find any correlation between Glt and GFR in predialysis patients, but there was direct dependance between Glt and tHcy plasma levels in this group. Glt plasma levels in dialysis patients were reliably lower than in predialysis ones. There was a lack of some correlation between Glt and tHcy in the haemodialysis group.
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