Petersen D J, Boniface A M, Schranck F W, Rupich R C, Whyte M P
Metabolic Research Unit, Shriners Hospital for Crippled Children, St. Louis, Missouri.
J Bone Miner Res. 1992 Jun;7(6):583-97. doi: 10.1002/jbmr.5650070602.
Not all children with X-linked hypophosphatemia (XLH) have demonstrated improved linear growth with calcitriol [1,25-(OH)2D3] and inorganic phosphate (Pi) therapy. To assess which factors are associated with a favorable growth response during this treatment, we retrospectively compared demographics and biochemical parameters of bone metabolism to the linear growth patterns of 20 children with XLH who were prepubertal and had not required osteotomy. A total of 15 patients had family histories consistent with XLH; 5 appeared to be sporadic cases. During 3 years of therapy, the growth velocities of 12 patients had been at or above the mean for age (good growers) and those of 8 patients had been below the mean (poor growers). Data from the two groups were contrasted. We found no difference between the good growers and poor growers before or after the 3 year period of therapy in mean age, dietary calcium, calcitriol dose or compliance, or Pi dose or compliance. Both groups increased their mean fasting serum Pi levels with treatment. The TmP/GFR (mean +/- SEM) of the good growers improved with therapy (1.9 +/- 0.2 to 2.6 +/- 0.2 mg/dl, p = 0.01), and their posttreatment value was higher compared to that of the poor growers (2.6 +/- 0.1 versus 2.2 +/- 0.1 mg/dl, p = 0.02). However, their enhanced TmP/GFR was not associated with a reduction in serum iPTH levels (before, 693 +/- 50; after, 688 +/- 76 pg/ml; p = 0.9). The Z test for binomial proportions showed that the group that grew well contained a disproportionate number of girls (10 of 12, p = 0.04). Our findings suggest that calcitriol may exert a direct effect on the renal tubule to improve Pi reclamation in XLH. The observation that heterozygous girls appear to respond better than hemizygous boys to calcitriol and Pi therapy provides evidence for a gene dosage effect in the expression of this X-linked dominant disorder.
并非所有患有X连锁低磷血症(XLH)的儿童在接受骨化三醇[1,25 -(OH)2D3]和无机磷酸盐(Pi)治疗后线性生长都得到改善。为了评估哪些因素与该治疗期间良好的生长反应相关,我们回顾性比较了20例青春期前且无需进行截骨术的XLH患儿的人口统计学和骨代谢生化参数与线性生长模式。共有15例患者的家族史符合XLH;5例似乎为散发病例。在3年的治疗期间,12例患者的生长速度达到或高于年龄均值(生长良好者),8例患者的生长速度低于均值(生长不良者)。对比了两组的数据。我们发现在治疗的3年期间之前或之后,生长良好者和生长不良者在平均年龄、饮食钙、骨化三醇剂量或依从性、Pi剂量或依从性方面均无差异。两组患者在治疗后平均空腹血清Pi水平均升高。生长良好者的TmP/GFR(均值±标准误)在治疗后得到改善(从1.9±0.2至2.6±0.2mg/dl,p = 0.01),且其治疗后的值高于生长不良者(2.6±0.1对2.2±0.1mg/dl,p = 0.02)。然而,他们增强的TmP/GFR与血清iPTH水平的降低无关(治疗前,693±50;治疗后,688±76pg/ml;p = 0.9)。二项式比例的Z检验表明,生长良好的组中女孩比例过高(12例中有10例,p = 0.04)。我们的研究结果表明,骨化三醇可能对肾小管产生直接作用以改善XLH患者的Pi重吸收。杂合子女孩似乎比半合子男孩对骨化三醇和Pi治疗反应更好这一观察结果为这种X连锁显性疾病表达中的基因剂量效应提供了证据。