AI Article Synopsis

  • The study investigates the effect of unripe banana flour (a prebiotic) on gut-derived metabolites associated with chronic kidney disease in patients undergoing peritoneal dialysis.
  • Although the primary outcomes showed no significant changes in serum levels of indoxyl sulfate, p-cresyl sulfate, and indole 3-acetic acid with the prebiotic treatment, a notable reduction in indoxyl sulfate levels was observed in a specific subgroup of participants who adhered closely to the dosage.
  • Overall, the findings suggest that while unripe banana flour may not provide widespread benefits for all participants, it could be beneficial for those who consume it as directed.

Article Abstract

In chronic kidney disease (CKD), the accumulation of gut-derived metabolites, such as indoxyl sulfate (IS), p-cresyl sulfate (pCS), and indole 3-acetic acid (IAA), has been associated with the burden of the disease. In this context, prebiotics emerge as a strategy to mitigate the accumulation of such compounds, by modulating the gut microbiota and production of their metabolites. The aim of this study was to evaluate the effect of unripe banana flour (UBF-48% resistant starch, a prebiotic) on serum concentrations of IS, pCS, and IAA in individuals undergoing peritoneal dialysis (PD). A randomized, double-blind, placebo-controlled, crossover trial was conducted. Forty-three individuals on PD were randomized to sequential treatment with UBF (21 g/day) and placebo (waxy corn starch-12 g/day) for 4 weeks, or vice versa (4-week washout). The primary outcomes were total and free serum levels of IS, pCS, and IAA. Secondary outcomes were 24 h urine excretion and dialysis removal of IS, pCS, and IAA, serum inflammatory markers [high-sensitivity C-reactive protein (hsCRP), interleukin-6 (IL-6), interleukin-10 (IL-10), and tumor necrosis factor-α (TNF-α)], serum lipopolysaccharide LPS, and dietary intake. Of the 43 individuals randomized, 26 completed the follow-up (age = 55 ± 12 years; 53.8% men). UBF did not promote changes in serum levels of IS ( = 0.70), pCS ( = 0.70), and IAA ( = 0.74). Total serum IS reduction was observed in a subgroup of participants ( = 11; placebo: median 79.5 μmol/L (31-142) versus UBF: 62.5 μmol/L (31-133), = 0.009) who had a daily UBF intake closer to that proposed in the study. No changes were observed in other secondary outcomes. UBF did not promote changes in serum levels of IS or pCS and IAA; a decrease in IS was only found in the subgroup of participants who were able to take 21g/day of the UBF.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922008PMC
http://dx.doi.org/10.3390/nu13020646DOI Listing

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