Rationale: Advanced glycation endproducts (AGEs) contribute to the pat
hogenesis of vascular complications in diabetes, aging and end-stage r
enal disease (ESRD). Immune abnormalities in patients with chronic ren
al failure and those treated by dialysis contribute to high rates of m
orbidity and mortality. We therefore sought a relationship between a c
irculating marker of immune dysfunction and plasma levels of the AGE p
entosidine. Method: We studied non-diabetic patients with mild to adva
nced renal failure (n = 60), and with ESRD treated by hemodialysis (HD
) (n = 44) and peritoneal dialysis (PD) (n = 19). The plasma protein c
ontent of the well characterized AGE, pentosidine was measured using H
PLC. In the same samples the monocyte activation product neopterin was
measured by RIA. Results: Plasma levels of pentosidine and neopterin
increased in parallel with the progression of renal failure. Pentosidi
ne and neopterin were highly correlated in all patients even after adj
ustment for Ccr. This correlation was also present in patients with ES
RD. Conclusion: These data suggest that the AGE pentosidine is associa
ted with monocyte activation in renal failure, an interaction which ma
y contribute to accelerated rates of complication and death by as yet
unknown mechanisms.