HYPERCALCEMIA DURING PULSE VITAMIN-D3 THERAPY IN CAPD PATIENTS TREATED WITH LOW-CALCIUM DIALYSATE - THE ROLE OF THE DECREASING SERUM PARATHYROID-HORMONE LEVEL
A. Chagnac et al., HYPERCALCEMIA DURING PULSE VITAMIN-D3 THERAPY IN CAPD PATIENTS TREATED WITH LOW-CALCIUM DIALYSATE - THE ROLE OF THE DECREASING SERUM PARATHYROID-HORMONE LEVEL, Journal of the American Society of Nephrology, 8(10), 1997, pp. 1579-1586
Oral pulse therapy with vitamin D is effective in suppressing parathyr
oid hormone (PTH) secretion in continuous ambulatory peritoneal dialys
is patients with secondary hyperparathyroidism (2'hpt). However, this
treatment often leads to hypercalcemia. The goals of the study were: (
1) to examine whether the incidence of hypercalcemia decreases when di
alysate calcium is reduced from 1.25 to 1.0 mmol/L; (2) to determine t
he relative role of the factors involved in the pathogenesis of hyperc
alcemia; and (3) to study the efficacy of a low oral pulse dose of alf
acalcidol in preventing the recurrence of 2'hpt. Fourteen continuous a
mbulatory peritoneal dialysis patients with 2'hpt were treated with pu
lse oral alfacalcidol and calcium carbonate and dialyzed with a 1.0-mm
ol (n = 7) or a 1.25-mmol (n = 7) dialysate calcium. The response rate
(87%) and the incidence (71%) and severity of hypercalcemia were simi
lar in both groups. In the early response stage, PTH decreased by 70%
in both groups, and serum ionized calcium (iCa) increased from 1.18 +/
- 0.02 to 1.27 +/- 0.04 mmol/L (P < 0.005) in the 1.0 group and from 1
.19 +/- 0.02 to 1.29 +/- 0.02 mmol/L in the 1.25 group (P < 0.005). Ni
ne of the 12 responders had a further decrease in serum PTH, which was
associated with an additional increase in iCa from 1.28 +/- 0.02 to 1
.47 +/- 0.04 (P < 0.005). Multivariate analysis showed that the early
increase in iCa was positively correlated with alfacalcidol dosage (r
= 0.69). In contrast, the late increase in iCa was mostly accounted fo
r by the decrease in serum PTH (r = -0.93). This occurred while calciu
m carbonate, alfacalcidol dosage, and serum 1,25 hydroxy D3 remained u
nchanged compared with the early response stage. Finally, an alfacalci
dol dose of 1 mu g twice weekly was unable to maintain serum PTH at an
adequate level in the long term. These data show that a reduction in
dialysate calcium from 1.25 to 1.0 mmol does not reduce the occurrence
of hypercalcemia and suggest that lowering serum PTH reduces the abil
ity of the bone to handle a calcium load within a few weeks, thus caus
ing hypercalcemia.