Mornière P, Maurouard C, Boudailliez B, Westeel P F, Achard J M, Boitte F, el Esper N, Compagnon M, Maurel G, Bouillon R
Service de Néphrologie, CHU d'Amiens, France.
Nephron. 1992;60(2):154-63. doi: 10.1159/000186732.
The purpose of this study is to evaluate the place of intravenous 1 alpha-hydroxyvitamin D3 (1 alpha-OH-D3) in the prevention of radiologically obvious hyperparathyroidism (HPT) in patients on maintenance dialysis while excluding aluminium phosphate binder and using a dialysate calcium concentration of 1.62 mmol which keeps the intradialytic calcium balance neutral. Therefore, 47 patients without subperiosteal resorption and previously treated by oral CaCO3 and if necessary Mg(OH)2 as phosphate binder while their dialysate calcium had a Ca level of 1.62 and a Mg level of 0.2 mmol/l were randomized into a control group of 24 who were maintained on the same treatment and an experimental group of 23. This group discontinued CaCO3 and received intravenous 1 alpha-OH-D3 after each dialysis at increasing doses up to 4 micrograms and increased Mg(OH)2 as their sole phosphate binder. When plasma Ca increased above 2.7 mmol/l, the dose of 1 alpha-OH-D3 was decreased. When plasma PO4 increased above 2 mmol/l, the dose of Mg(OH)2 was increased to the highest dose not inducing diarrhea, hypermagnesemia (less than 2 mmol/l) or hyperkalemia (less than 6 mmol/l). In case of persistent hyperphosphatemia, the dose of 1 alpha-OH-D3 was decreased. Since mean plasma alkaline phosphatase was normal, HPT was monitored on the plasma concentration of 1-84 PTH for which a previous histological study showed that frank osteitis fibrosa was present only when they were above 70 pg/ml, i.e. (about twice the upper limit of the normal value). Before the study, plasma PTH was below this limit in 16 patients of the CaCO3 group and in 14 patients of the 1 alpha-OH-D3 group. After 6 months, they remained below this limit in all patients except 2 of each group. Plasma PTH was initially above 70 pg/ml in 8 of the CaCO3 and did not change significantly throughout the study, 2 patients having at 6 months a PTH level below 70 pg/ml. In contrast with intravenous 1 alpha-OH-D3, all the 9 patients with initial frank HPT decreased their PTH levels after 2 months, the levels being below 70 pg/ml in 6 cases. However, because of hypercalcemia and/or of hyperphosphatemia in spite of a highest tolerable dose of Mg(OH)2, 1 alpha-OH-D3 doses had to be decreased down to 0.4 microgram per dialysis at the 6th month so that at 6 months 6 of 9 patients had their PTH levels above 70 pg/ml, a number comparable to that of patients treated with CaCO3 (6 of 8).(ABSTRACT TRUNCATED AT 400 WORDS)
本研究的目的是评估静脉注射1α-羟维生素D3(1α-OH-D3)在维持性透析患者中预防放射学上明显的甲状旁腺功能亢进(HPT)的作用,同时排除磷酸铝结合剂,并使用钙浓度为1.62 mmol的透析液,以保持透析期间的钙平衡为中性。因此,47例无骨膜下吸收且先前接受过口服碳酸钙治疗的患者,必要时使用氢氧化镁作为磷结合剂,其透析液钙水平为1.62,镁水平为0.2 mmol/L,被随机分为对照组24例,维持相同治疗,以及实验组23例。该组停用碳酸钙,每次透析后接受静脉注射1α-OH-D3,剂量逐渐增加至4微克,并增加氢氧化镁作为唯一的磷结合剂。当血浆钙升高至2.7 mmol/L以上时,降低1α-OH-D3的剂量。当血浆磷升高至2 mmol/L以上时,将氢氧化镁的剂量增加至不引起腹泻、高镁血症(低于2 mmol/L)或高钾血症(低于6 mmol/L)的最高剂量。如果持续性高磷血症,降低1α-OH-D3的剂量。由于平均血浆碱性磷酸酶正常,通过监测血浆1-84 PTH浓度来监测HPT,先前一项组织学研究表明,只有当血浆1-84 PTH高于70 pg/ml时(即约为正常值上限的两倍)才会出现明显的纤维性骨炎。研究前,碳酸钙组16例患者和1α-OH-D3组14例患者的血浆PTH低于此限值。6个月后,除每组各2例患者外,所有患者的血浆PTH仍低于此限值。碳酸钙组8例患者的血浆PTH最初高于70 pg/ml,在整个研究过程中无显著变化,2例患者在6个月时PTH水平低于70 pg/ml。与静脉注射1α-OH-D3相反,9例初始有明显HPT的患者在2个月后其PTH水平均下降,6例患者的水平低于70 pg/ml。然而,由于尽管使用了最高耐受剂量的氢氧化镁仍出现高钙血症和/或高磷血症,1α-OH-D3的剂量在第6个月不得不降至每次透析0.4微克,因此在6个月时,9例患者中有6例的PTH水平高于70 pg/ml,这一数字与使用碳酸钙治疗的患者(8例中的6例)相当。(摘要截断于400字)