Chronic
uremia is characterized by decreased levels of plasma
1,25(OH)2D3 due to decreased renal 1-hydroxylase activity and by decreased renal
phosphate excretion. The consequence is an increased synthesis and secretion of
parathyroid hormone--
secondary hyperparathyroidism--due to the low levels of plasma
calcium, low levels of plasma
1,25(OH)2D3 and high levels of
phosphate. The association between renal
bone disease and
chronic renal failure is well described. Epidemiological studies have indicated that an association also exists between
secondary hyperparathyroidism and increased mortality and cardiovascular calcifications in chronic uremic patients. Treatment of
secondary hyperparathyroidism in chronic
uremia focuses on avoiding
hyperphosphatemia by the use of oral
phosphate binders, which bind
phosphate in the intestine and a concomitant substitution by a 1 alpha-hydroxylated
vitamin D analog in order to compensate for the reduced renal hydroxylation. Additional treatment with
aluminum containing
phosphate binders to overcome
phosphate absorption and retention was initiated already in the 1960s and used extensively until
aluminum toxicity was disclosed in the mid-1980s. Instead
calcium carbonate and
calcium acetate were used as
phosphate binders. Until recently, the most commonly used active
vitamin D drug was either the natural
1,25(OH)2D3, or the 1 alpha-hydroxylated analog, 1alpha(
OH)D3 which after 25-hydroxylation in the liver is converted to
1,25(OH)2D3. 1alpha(
OH)D3 was produced by LEO Pharma in 1973. The two
vitamin D analogs were used in different geographical areas: In Europe 1alpha(
OH)D3 was mainly used, while
1,25(OH)2D3 was mainly used in the USA.
1,25(OH)2D3 increases the intestinal absorption of
calcium and improves skeletal abnormalities. The combined treatment with
calcium containing
phosphate binders and active
vitamin D induces an increase in plasma Ca 2+ and
hypercalcemia became a clinical problem. Subsequently therefore, dialysis fluid with a reduced
calcium concentration ("low-
calcium") was introduced. In 1981 Madsen et al. [148] demonstrated for the first time a direct suppressive effect of intravenous
1,25(OH)2D3 on plasma PTH in acutely uremic patients. In 1984, Slatopolsky et al. [74] demonstrated that intravenous
1,25(OH)2D3 induces a marked suppression of plasma PTH with no increase in plasma Ca 2+ in chronic uremic patients. In the middle of the 1980s, 1alpha(
OH)D3 became available not only as an oral, but also as an intravenous formulation. The main purpose of the present studies was to increase the knowledge of the action and effects of different treatment regimes with 1alpha(
OH)D3, and thereby to improve the prophylaxis and treatment of
secondary hyperparathyroidism in uremic patients on chronic dialysis. 168 patients on chronic dialysis treatment and six healthy volunteers were included in the seven studies included in this thesis. The first part of the studies, focused on short- (12 weeks) and long-term (103 weeks) effects of intravenous 1alpha(
OH)D3 on plasma PTH and plasma Ca 2+ in relation to the doses of 1alpha(
OH)D3 given. Further, it was examined whether the marked suppression of plasma PTH induced by 300 days of intermittent intravenous treatment with 1alpha(
OH)D3, could be maintained when the administration was changed from intravenous to the oral route for 16 further weeks and then shifted back to
intravenous administration for another 16 weeks. The second part focused on long-term effects (88 weeks in
hemodialysis patients and 52 weeks in
CAPD patients) of a treatment modality combining 1alpha(
OH)D3, and CaCO3 as
phosphate binders instead of
aluminum containing compounds and a decreased
calcium concentration in the dialysis fluid to 1.25 mmol/l in an attempt to avoid development of
hypercalcemia. The third part focused upon the pharmacokinetic differences between intravenous and
oral administration of
1,25(OH)2D3 and 1alpha(
OH)D3 and upon the acute effects of different doses of the two compounds on the plasma levels of PTH, Ca 2+ and
phosphate. Plasma PTH is a biochemical parameter most often used for the diagnosis and monitoring of
bone disease in patients with chronic
uremia. The level of plasma PTH measures depends on the assay used. More specific assays measuring only whole
PTH 1-84 without co-measuring large C-terminal fragments have been developed. In this thesis, five different assays were used - one "N-terminal", one "C-terminal", two "Intact" and one "Whole" PTH assay. Each sample was analyzed by 1-3 different assays. Based on the results of my studies [1-7], it is concluded that: 1a.
Intravenous administration of 1alpha(
OH)D3 induces a marked suppression of plasma PTH without causing serious side-effects in patients on chronic
hemodialysis. It is possible to prevent
hypercalcemia by closely monitoring plasma Ca 2+ levels and by adjusting the dose of 1alpha(
OH)D3 accordingly. 1b. Long-term intermittent intravenous treatment with 1alpha(
OH)D3 was effective in suppressing plasma levels of Intact PTH. 1c. When plasma intact PTH was suppressed to a stable level by intravenous 1alpha(
OH)D3 the suppression could be maintained by intermittent oral 1alpha(
OH)D3
therapy. It was not examined whether a similar degree of suppression of severe
secondary hyperparathyroidism could be induced by intermittent oral 1alpha(
OH)D3 treatment alone. The responses following chronic intravenous or
oral administration of 1alpha(
OH)D3 on circulating levels of intact PTH and N- and
C-terminal PTH fragments did not reveal any significant differences between the two routes of administration on the actions on the parathyroid glands. 2a. The combination of "low-
calcium"
hemodialysis fluid (1.25 mmol/l), CaCO3 as a
phosphate binder, and intermittent intravenous 1alpha(
OH)D3 prevented development of
secondary hyperparathyroidism in uremic patients with normal PTH at the initiation of the study and induced a long-term suppression of PTH in patients with
secondary hyperparathyroidism. No clinical or biochemical indications of development of adynamic
bone disease were observed.
Intravenous administration of 1alpha(
OH)D3 prevented a decrease of BMC in the lumbar spine and femoral neck of
hemodialysis patients both with normal and with elevated PTH levels. It was possible to use larger doses of CaCO3 and to reduce, but not exclude, the use of
aluminum-containing
phosphate binders in combination with
intravenous administration of 1alpha(
OH)D3. A decrease of plasma Ca 2+ was induced during dialysis, and special care had to be taken on the compliance of the patients as to the use of CaCO3 binders in order not to aggravate
secondary hyperparathyroidism. 2b. In patients on
CAPD, the use of low-
calcium dialysis (1.25 mmol/l) made it possible to use larger doses of CaCO3
phosphate binders and to reduce, but not exclude, the use of
aluminium containing
phosphate binder in combination with oral pulses of 1alpha(
OH)D3. A negative
calcium balance was induced, and it is therefore recommended that a reduction of the
calcium concentration in the dialysis fluid is only used in patients under strict control. 3a. The metabolic clearance rate of
1,25(OH)2D3 was 57% lower in uremic patients than in normal subjects (p < 0.03). The bioavailability of
1,25(OH)2D3 in both normal subjects and uremic patients was markedly lower following administration of 1alpha(
OH)D3 both intravenously and orally than after administration of oral
1,25(OH)2D3. Despite lower plasma
1,25(OH)2D3 levels after administration of 1alpha(
OH)D3 than after
1,25(OH)2D3, no significant difference was observed in the PTH suppressive effect in uremic patients of 4 mug intravenously of either of the two
vitamin D analogs. 3b. A single intravenous high dose of 10 mug of 1alpha(
OH)D3 or
1,25(OH)2D3 significantly suppressed plasma PTH. The acute suppressive effect of
1,25(OH)2D3 was three times greater than that of 1alpha(
OH)D3.The increase in plasma Ca 2+ after
intravenous administration of 10 mug
1,25(OH)2D3 was significantly higher than that of 1alpha(
OH)D3. Due to the simultaneous effect on plasma Ca 2+ observed it was not possible to decide whether 1alpha(
OH)D3 has a direct effect per se on the parathyroid glands or not. The study further did not give any further knowledge about the possible therapeutic equivalence of long-term treatment with 1alpha(
OH)D3 or
1,25(OH)2D3. The PTH responses to acute administration of the 1alpha(
OH)D3 and
1,25(OH)2D3 analogs were in principle the same when measured by one "whole" PTH and two "intact" PTH assays, namely mainly in a parallel shift of the PTH response curve. In this study on chronic uremic patients circulating levels of large
C-terminal PTH fragments were not affected by differences in plasma Ca 2+ concentration or by the
intravenous administration of 1alpha(
OH)D3 or
1,25(OH)2D3. There is now a general agreement on the importance of carefully controlling plasma
phosphate, normalize and avoid increases of plasma Ca 2+, and not to oversuppress PTH during treatment. Focus today is on the potential deleterious role of
calcium overloading in the development of
vascular calcifications in uremic patients. There is an urgent need for a development of an algorithm for the use of
phosphate binders and
vitamin D supplementation in combination with calcimimetics focusing upon long term morbidity and mortality in uremic patients.