Djukanović L, Pejanović S, Dragojlović Z, Stosović M
Institute of Urology and Nephrology, University Clinical Center, Beograd, Yugoslavia.
Ren Fail. 1994 Nov;16(6):715-23. doi: 10.3109/08860229409044901.
The present study examined the effect of intermittent oral high doses of 1-alpha-OHD3 in combination with a pharmacological dose of 24,25(OH)2D3 on parathyroid hormone (PTH) secretion. Twenty hemodialysis (HD) patients (10 males, aged 26-72 years, on regular hemodialysis for 7-128 months) with secondary hyperparathyroidism resistant to long-term low-dose 1-alpha-OHD3 therapy were studied for 24 weeks. At the outset of the study they were randomly divided into two groups: group 1 received high-dose 1-alpha-OHD3 plus 24,25(OH)2D3 (2 x 5 micrograms/day) and group 2 was on monotherapy with 1-alpha-OHD3. 1-alpha-OHD3 was given three times a week in the evening before each HD in gradually increased doses from 1 to 4 micrograms adjusted to keep serum calcium levels below 2.6 mmol/L. During the therapy mean serum calcium and ionized calcium levels increased but remained in the normal ranges without differences between the two groups. However, the frequency of hypercalcemia episodes was different in the two groups. In the first 12 weeks the number of hypercalcemia episodes was significantly lower in group 1 than in group 2 (6 vs. 12; p < .05), allowing the use of significantly higher 1-alpha-OHD3 doses in group 1. In the second 12 weeks of the study the 1-alpha-OHD3 dose in group 1 had to be reduced due to more frequent appearance of hypercalcemia. So, the 1-alpha-OHD3 doses became similar in the two groups during the second 12 weeks of the study.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究检测了间歇性口服高剂量1-α-羟维生素D3联合药理剂量的24,25-二羟维生素D3对甲状旁腺激素(PTH)分泌的影响。对20例长期低剂量1-α-羟维生素D3治疗抵抗的继发性甲状旁腺功能亢进血液透析(HD)患者(10例男性,年龄26 - 72岁,规律血液透析7 - 128个月)进行了为期24周的研究。研究开始时,他们被随机分为两组:第1组接受高剂量1-α-羟维生素D3加24,25-二羟维生素D3(2×5微克/天),第2组接受1-α-羟维生素D3单药治疗。1-α-羟维生素D3每周给药3次,于每次HD前的晚上服用,剂量从1微克逐渐增加至4微克,并进行调整以保持血清钙水平低于2.6毫摩尔/升。治疗期间,两组的平均血清钙和离子钙水平均升高,但仍保持在正常范围内,且两组之间无差异。然而,两组高钙血症发作的频率不同。在最初的12周内,第1组高钙血症发作的次数显著低于第2组(6次对12次;p<0.05),使得第1组能够使用显著更高剂量的1-α-羟维生素D3。在研究的第二个12周,由于高钙血症更频繁出现,第1组的1-α-羟维生素D3剂量不得不降低。因此,在研究的第二个12周,两组的1-α-羟维生素D3剂量变得相似。(摘要截选至250字)