2023
DOI: 10.1016/j.xkme.2023.100645
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The Gut-Peritoneum Axis in Peritoneal Dialysis and Peritoneal Fibrosis

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Cited by 6 publications
(2 citation statements)
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“…Instead, it is influenced by the individualized dialysis prescription and the clinical characteristics of each PD patient. Additionally, studies have established correlations between the gut microbiota composition and factors such as the duration of dialysis treatment (dialysis vintage), the level of residual kidney function, and the extent of peritoneal glucose exposure in PD patients ( Stepanova, 2023 ). Prolonged dialysis sessions, elevated peritoneal glucose exposure, and the decline in residual renal function have been linked to changes in gut microbial composition and a decrease in the production of branched-chain short-chain fatty acids among PD patients.…”
Section: Inter-organ Communicationmentioning
confidence: 99%
“…Instead, it is influenced by the individualized dialysis prescription and the clinical characteristics of each PD patient. Additionally, studies have established correlations between the gut microbiota composition and factors such as the duration of dialysis treatment (dialysis vintage), the level of residual kidney function, and the extent of peritoneal glucose exposure in PD patients ( Stepanova, 2023 ). Prolonged dialysis sessions, elevated peritoneal glucose exposure, and the decline in residual renal function have been linked to changes in gut microbial composition and a decrease in the production of branched-chain short-chain fatty acids among PD patients.…”
Section: Inter-organ Communicationmentioning
confidence: 99%
“…Besides miR-15a-5p, peritoneal fibrosis is also modulated by miR-199a-5p, miR-214-3p, miR-30a, miR-153-3p, miR-21, miR-129-5p, miR-30b, miR-200, miR-145, miR-302c, miR-34a, and miR-29b [ 25 , 26 ]. Recently, the potential link between the intestinal microbiota and dysbiosis with peritoneal fibrosis has been discussed, in which several molecular and cellular mechanisms are likely to contribute to the formation of peritoneal fibrosis, for example, gut-sourced metabolites (e.g., short-chain fatty acids (SCFA) and lipopolysaccharides (LPS)), inflammation, production of reactive oxygen species and oxidative stress, activation of the host immune response, and intestinal bacterial translocation [ 27 ].…”
Section: The Pathophysiology Of Peritoneal Fibrosismentioning
confidence: 99%