Uremic toxicity is related in part to the accumulation of toxic substances,
the nature of which has only partly been characterized. Because of the use
of a highly permeable membrane and better preservation of the residual ren
al function, it could be anticipated that some of these uremic toxins are m
ore efficiently cleared across the peritoneal membrane, and that the plasma
and tissue levels of these compounds are lower than in hemodialysis patien
ts. This article analyzes the generation and removal of several uremic toxi
ns in peritoneal dialysis patients. The following uremic toxins are discuss
ed: beta (2)-microglobulin, advanced glycation end products, advanced oxida
tion protein products, granulocyte inhibitory proteins, p-Cresol, and hyper
homocysteinemia. Some recent studies are reviewed suggesting that uremic to
xins are involved in the progression of renal failure and are at least part
ially removed by peritoneal dialysis. We conclude that, although the plasma
levels of some of these compounds are lower in peritoneal dialysis versus
hemodialysis patients, it does not mean that the peritoneal dialysis patien
t is "better" protected against the numerous disturbances caused by these t
oxins.