Diurnal Variation of Uremic Solutes in Peritoneal Dialysis
|Chronic Kidney Disease|
|Study Design:||Observational Model: Case Control
Time Perspective: Cross-Sectional
|Official Title:||Diurnal Variation of Mineral Metabolism and Protein Fermentation Metabolites in Peritoneal Dialysis Patients and Healthy Volunteers|
- To evaluate the diurnal variation of serum concentrations of phosphate and protein fermentation metabolites in healthy volunteers as compared to dialysis patients. [ Time Frame: 4 months ]
Biospecimen Retention: Samples Without DNA
|Study Start Date:||February 2010|
|Study Completion Date:||December 2012|
|Primary Completion Date:||December 2012 (Final data collection date for primary outcome measure)|
chronic kidney disease
ESKD patients treated with peritoneal dialysis
healthy volunteers, aged 18 years and above
Many epidemiological studies have pointed to the association between serum parameters of phosphate metabolism (phosphate, FGF23) and microbiotic protein fermentation (p-cresyl sulphate [PCS], indoxyl sulphate [IS]) on the one hand and increased risk of all-cause and cardiovascular death on the other hand.
Hypothesis: Due to failing feed-back mechanisms, diurnal variation of serum concentrations of serum phosphate and fermentation metabolites will be more pronounced in dialysis patients, especially in those with negligible residual kidney function.
Clinical studies assessing this issue are scarce to non-existing.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01093456
|Leuven, Vlaams-Brabant, Belgium, 3000|
|Principal Investigator:||Pieter Evenepoel, MD, PhD||UZ Leuven|