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Published on: July 19, 2018
Proteome profile of peritoneal effluents in children on glucose- or icodextrin-based peritoneal dialysis
Maurizio Bruschi1, Giovanni Candiano, Laura Santucci
1Renal Child's Foundation, Genoa, Italy. mauriziobruschi@yahoo.it
Insights
Icodextrin (Ico) solution shows improved removal of small proteins compared to glucose (Glu) in pediatric peritoneal dialysis. However, Ico also removes more oxidized albumin, with unknown long-term clinical effects.
Area of Science:
- Proteomics
- Biochemistry
- Nephrology
Background:
- Peritoneal dialysis (PD) utilizes icodextrin (Ico) or glucose (Glu) solutions.
- Understanding protein profiles and redox status in PD effluents is crucial.
Purpose of the Study:
- Compare proteome profiles and protein oxido-redox status in peritoneal effluents from pediatric patients using Ico versus Glu solutions.
- Assess the efficiency of Ico and Glu in removing specific proteins.
Main Methods:
- Two-dimensional electrophoresis and mass spectrometry analyzed protein composition in effluents from 16 pediatric patients undergoing 14-hour daytime PD dwells.
- Cyanine labeling quantified oxidized protein products.
- Compared protein removal kinetics for β2-microglobulin and cystatin C.
Main Results:
- Icodextrin demonstrated significantly higher peritoneal transport of β2-microglobulin and cystatin C compared to glucose.
- Proteome analysis revealed more protein spots in Ico effluents, with 314 spots significantly higher than in Glu effluents.
- Greater amounts of oxidized albumin were found in Ico dialysate, correlating with lower serum albumin levels.
Conclusions:
- Icodextrin solution is more efficient in removing small proteins during peritoneal dialysis in pediatric patients.
- The removal of larger proteins and their oxidized forms by Ico may have complex effects.
- Long-term clinical implications of removing specific molecules, including oxidized proteins, require further investigation.
Background:
We compared the proteome profile of peritoneal effluents obtained with icodextrin (Ico) or glucose (Glu) in paediatric patients and defined the oxido-redox status of proteins.
Methods:
Sixteen patients underwent two 14-h daytime dwells performed on subsequent days with 7.5% Ico and 3.86% Glu solutions. Protein composition was analysed by two-dimensional electrophoresis and mass spectrometry; oxidized products were evaluated by cyanine labelling.
Results:
Peritoneal transport kinetics of β2-microglobulin and cystatin C was linear for both solutions, but was significantly higher with Ico than with Glu, suggesting a better efficiency for these molecules. There was a linear correlation between total protein removal during Ico and Glu dialysis in the same patient, suggesting that it is a function of peritoneal membrane characteristics. The ratio between proteins removed by Ico and by Glu solutions was higher at low removal rate. Image gel analysis revealed 1064 and 774 spots, respectively, in Ico and Glu solutions; 524 were common, and 314 were higher in Ico than Glu effluents. Analysis of protein oxido-redox status showed a greater amount of oxidized albumin in Ico dialysate that was correlated with lower serum levels.
Conclusions:
Our results indicate a better efficiency of Ico in removing small proteins. Removal of big proteins and their oxidized isoforms reflects potentially opposite effects. The long-term clinical consequences of removing also potentially important molecules are to be defined.
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