Chronic kidney disease is associated with the accumulation of various metabolites, i.e., uremic retention solutes. Evidence is mounting that the colonic microbiome contributes substantially to these uremic retention solutes. Indoxyl sulfate and p-cresyl sulfate are among the most extensively studied gut microbial metabolites, and are associated with cardiovascular disease, chronic kidney disease progression and overall mortality. Colonic transit time is an important determinant of intestinal generation and uptake of bacterial metabolites. However, it is unknown if accelerating the colonic transit time reduces the intestinal generation and uptake of indoxyl sulfate and p-cresyl sulfate. Prucalopride is a selective, high-affinity 5-HT4 receptor agonist with a stimulating effect on colonic motility and transit. It is currently used in treating chronic slow-transit constipation. An observational study will be initiated in non-chronic kidney disease patients with chronic slow-transit constipation necessitating treatment with prucalopride to observe its effect on serum concentrations and intestinal generation of indoxyl sulfate and p-cresyl sulfate.
Study Type
OBSERVATIONAL
Treatment with prucalopride for slow-transit constipation
University Hospitals Leuven
Leuven, Vlaams-Brabant, Belgium
change in serum concentration of bacterial metabolites
change in serum concentration of bacterial metabolites before and after (4 weeks) treatment of prucalopride
Time frame: 4 weeks
change in 24h urinary excretion rate of bacterial metabolites
change in 24h urinary excretion rate of bacterial metabolites before and after (4 weeks) treatment of prucalopride
Time frame: 4 weeks
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