G. Bereket et al., PERITONEAL LOSS OF INSULIN-LIKE GROWTH-FACTOR-I AND BINDING-PROTEINS IN END-STAGE RENAL-DISEASE, Pediatric nephrology, 12(7), 1998, pp. 581-588
The kinetics of peritoneal transport of insulinlike growth factor (IGF
) system-related proteins during dialysis is not well characterized. W
e studied temporal changes in dialysate and serum concentrations of IC
E-I and IGF-II as well as IGF binding protein (BP)-1, -2, and -3 in te
n children with end-stage renal disease (ESRD) undergoing continuous c
ycling peritoneal dialysis (CCPD) during a 4-h peritoneal equilibratio
n test (PET). Dialysate concentrations of IGF-I, IGF-II, and all three
IGFBPs demonstrated a time-dependent increase during PET. Despite the
ir transport, the serum concentrations of these proteins did not chang
e significantly during the PET. Dialysate/serum ratios for IGF-I, IGF-
II, and IGFBP-1, -2, and -3 were significantly increased at 2 h and in
creased further at 4 h, at which time values averaged 1.3+/-0.2%, 3.1/-0.5%, 6.2+/-1.0%, 2.4+/-0.2%, and 1.3+/-0.2% of serum levels, respec
tively. The transperitoneal clearance (mu l/min per 1.73 m(2)) of the
three IGFBPs was inversely related to both their molecular weight and
plasma concentration. However, peritoneal clearance of IGF-I and -II w
as similar to that of the larger and more-abundant IGFBP-3. Mass trans
fer rates (mu g/h per 1.73 m2) for the IGFs and their binding proteins
were directly proportional to their prevailing plasma concentration.
Based on estimates of mass transfer, only a small molar excess of IGFB
Ps was removed from the circulation relative to the combined molar con
centration of IGF-I and ICE-II. Hence, it seems unlikely that any bene
ficial effect of CCPD on growth in children with ESRD is mediated via
a preferential loss of IGFBPs into the dialysate fluid.