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Lipid and immunophenotypic profiles in hemodialysis patients with citrate vs. acetate dialysates
Diana Rodríguez-Espinosa1,2, Elena Cuadrado-Payán2, Laura Morantes2
1Departament de Medicina, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), Barcelona, Spain.
Insights
Citrate dialysate significantly altered lipid profiles and immune cells in dialysis-dependent chronic kidney disease (DD-CKD) patients. While it reduced triglycerides and remnant cholesterol, further research is needed to confirm clinical benefits.
Area of Science:
- Nephrology
- Immunology
- Cardiovascular Medicine
Background:
- Dialysis-dependent chronic kidney disease (DD-CKD) significantly increases cardiovascular risk.
- Hypercholesterolemia is a major cardiovascular risk factor, but statin efficacy in DD-CKD is unclear.
- Citrate dialysate may offer benefits over acetate dialysate by modulating inflammatory and lipid profiles.
Purpose of the Study:
- To investigate the impact of citrate versus acetate dialysate on lipid profiles.
- To assess the effects of citrate versus acetate dialysate on immunophenotypes in DD-CKD patients.
Main Methods:
- A unicentric, cross-over, prospective study involving 21 DD-CKD patients.
- Patients underwent 12 dialysis sessions with citrate dialysate and 12 with acetate dialysate, acting as their own controls.
- Lipid profiles, immunological parameters, and inflammatory markers were measured.
Main Results:
- Citrate dialysate led to significant reductions in triglycerides and remnant cholesterol, alongside decreases in HDL and increases in LDL.
- Immunologically, citrate dialysate showed higher C3 complement levels but lower CD3+ CD8+ and CD16+ 56+ lymphocytes.
- Erythrocyte Sedimentation Rate (ESR) was higher with citrate dialysate, while other nutritional and inflammatory markers showed no significant difference.
Conclusions:
- Citrate dialysate induces distinct changes in lipid and immunophenotypic profiles compared to acetate dialysate.
- The observed reduction in remnant cholesterol and triglycerides with citrate dialysate may be beneficial.
- Further studies are required to determine if these alterations translate to improved clinical outcomes in DD-CKD patients.
Background:
Chronic kidney disease (CKD) is a significant cardiovascular (CV) risk factor, with dialysis-dependent CKD (DD-CKD) patients facing high mortality rates. Hypercholesterolemia is another crucial CV risk factor, typically managed with lipid-lowering therapy, though its efficacy in DD-CKD remains uncertain. Evidence shows mixed results regarding the benefits of statins in these patients. Citrate-based dialysates are known to reduce inflammatory biomarkers compared to acetate-based ones, potentially impacting lipid profiles and immune responses. This study aimed to determine the effects of citrate vs. acetate dialysate on lipid profiles and immunophenotypes in DD-CKD patients.
Methods:
This unicentric, cross-over, prospective study included 21 hemodialysis patients (10 males, 11 females, average age 62.25 years). Each patient underwent 24 dialysis sessions (12 with each dialysate) and acted as their own control. Lipid profiles, immunological parameters, and nutritional and inflammatory markers were measured before the last session with each dialysate.
Results:
After twelve dialysis sessions with citrate dialysate (CD), compared to acetate dialysate (AD), there was a statistically significant decline in TG and remnant cholesterol, with a decrease in HDL and an increase in LDL. Regarding immunology, C3 complement levels were higher, while CD3+ CD8+ and CD16+ 56+ lymphocytes were lower. Finally, total lymphocytes were lower with AD than with CD. We found no difference in predialysis nutritional nor inflammatory parameters except for ESR, which was higher when subjects used CD than AD.
Conclusion:
There are significant differences in lipid and immunophenotypic profiles with CD in comparison to AD. Interestingly, there could be an advantageous profile given the reduced amount of remnant cholesterol and TG. However, further studies are needed to understand if the observed changes lead to beneficial hard clinical outcomes in DD-CKD patients.
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