Patel L, Clayton P E, Brain C, Pelekouda E, Addison G M, Price D A, Mughal M Z
Department of Child Health, University of Manchester, UK.
Clin Endocrinol (Oxf). 1996 Jun;44(6):687-96. doi: 10.1046/j.1365-2265.1996.740561.x.
Conventional treatment of familial hypophosphaiaemic rickets with oral phosphate and 1 alpha-hydroxycholecalciferol (1 alpha HCC) does not satisfactorily correct the metabolic or physical defects of the disease and can have adverse effects, such as nephrocalcinosis. Hyperoxaluria from increased oral phosphate intake may contribute to nephrocalcinosis. Growth hormone enhances renal tubular phosphate reabsorption and 1,25-dihydroxy-cholecalciferol production in normal and in GH deficient individuals, and may thus be of benefit to patients with familial hypophosphataemic rickets.
We have assessed the acute effects of GH on phosphate and calcium metabolism in 6 children (age 4-14 years) with familial hypophosphataemic rickets.
Each patient served as his/her own control and received the following in a sequential non-randomized design: conventional treatment with oral phosphate 1.0-3.4 mmol/kg/day in 3-6 divided doses and 1 alpha HCC 18-31 ng/kg/day-no treatment-GH 0.05 mg/kg daily-GH and 1 alpha HCC-and GH with phosphate and 1 alpha HCC. Each treatment was given for 7 days with 7 day periods of no treatment in between.
Glomerular filtration rate, tubular maximum rate of phosphate reabsorption per litre of glomerular filtrate (TmP/GFR) and serum 1,25-dihydroxycholecalciferol increased with GH. Mean 24-hour plasma phosphate concentrations did not increase with GH but were higher in the treatment phases which included phosphate and 1 alpha HCC (P = 0.002). Serum PTH was higher when GH was given in combination with phosphate and 1 alpha HCC compared to other phases. Urine oxalate excretion did not differ between the treatment phases.
GH seemed to partially correct the defects in renal tubular phosphate transport and 1 alpha-hydroxylation of 25-hydroxycholecalciferol. We speculate that the net effect of GH treatment was an increase in body phosphate, although this was not reflected in a change in plasma phosphate. Therefore, GH in combination with 1 alpha HCC may act as a phosphate sparing agent, permitting treatment with lower and less frequent doses of oral phosphate and reducing adverse effects such as nephrocalcinosis.
采用口服磷酸盐和1α-羟胆钙化醇(1α-HCC)对家族性低磷性佝偻病进行常规治疗,无法令人满意地纠正该疾病的代谢或身体缺陷,且可能产生诸如肾钙质沉着症等不良反应。口服磷酸盐摄入量增加导致的高草酸尿症可能会促使肾钙质沉着症的发生。生长激素可增强正常个体以及生长激素缺乏个体的肾小管对磷酸盐的重吸收和1,25-二羟胆钙化醇的生成,因此可能对家族性低磷性佝偻病患者有益。
我们评估了生长激素对6名患有家族性低磷性佝偻病的儿童(年龄4 - 14岁)的磷酸盐和钙代谢的急性影响。
每位患者均作为自身对照,采用序贯非随机设计接受以下治疗:口服磷酸盐1.0 - 3.4 mmol/kg/天,分3 - 6次给药,以及1α-HCC 18 - 31 ng/kg/天进行常规治疗 - 不治疗 - 每天给予生长激素0.05 mg/kg - 生长激素与1α-HCC联合使用 - 生长激素与磷酸盐和1α-HCC联合使用。每种治疗持续7天,期间间隔7天不进行治疗。
生长激素可使肾小球滤过率、每升肾小球滤液中磷酸盐的最大肾小管重吸收率(TmP/GFR)以及血清1,25-二羟胆钙化醇升高。24小时血浆磷酸盐平均浓度并未随生长激素升高,但在包含磷酸盐和1α-HCC的治疗阶段更高(P = 0.002)。与其他阶段相比,生长激素与磷酸盐和1α-HCC联合使用时血清甲状旁腺激素更高。各治疗阶段的尿草酸排泄无差异。
生长激素似乎部分纠正了肾小管磷酸盐转运和25-羟胆钙化醇1α-羟化的缺陷。我们推测生长激素治疗的净效应是体内磷酸盐增加,尽管这并未反映在血浆磷酸盐的变化上。因此,生长激素与1α-HCC联合使用可能作为一种磷节约剂,允许使用更低剂量且给药频率更低的口服磷酸盐进行治疗,并减少诸如肾钙质沉着症等不良反应。