Drezner M K, Lyles K W, Haussler M R, Harrelson J M
J Clin Invest. 1980 Nov;66(5):1020-32. doi: 10.1172/JCI109930.
Although a defect in renal transport of phosphate seems well established as the primary abnormality underlying the pathogenesis of X-linked hypophosphatemic rickets and osteomalacia, several observations indicate that renal phosphate wasting and hypophosphatemia cannot solely account for the spectrum of abnormalities characteristic of this disease. Thus, in the present study, we investigated the potential role of abnormal vitamin D metabolism in the pathogenesis of this disorder and the effect of 1,25-dihydroxyvitamin D(3) therapy on both the biochemical abnormalities characteristic of this disease and the osteomalacia. Four untreated patients, ages 14-30 yr, had normocalcemia (9.22+/-0.06 mg/dl); hypophosphatemia (2.25+/-0.11 mg/dl); a decreased renal tubular maximum for the reabsorption of phosphate per liter of glomerular filtrate (2.12+/-0.09 mg/dl); normal serum immunoreactive parathyroid hormone concentration; negative phosphate balance; and bone biopsy evidence of osteomalacia. The serum 25-hydroxyvitamin D(3) concentration was 33.9+/-7.2 ng/ml and, despite hypophosphatemia, the serum level of 1,25-dihydroxyvitamin D(3) was not increased, but was normal at 30.3+/-2.8 pg/ml. These data suggested that abnormal homeostasis of vitamin D metabolism might be a second defect central to the phenotypic expression of X-linked hypophosphatemic rickets/osteomalacia. This hypothesis was supported by evaluation of the long-term response to pharmacological amounts of 1,25-dihydroxyvitamin D(3) therapy in three subjects. The treatment regimen resulted in elevation of the serum 1,25-dihydroxyvitamin D levels to values in the supraphysiological range. Moreover, the serum phosphate and renal tubular maximum for the reabsorption of phosphate per liter of glomerular filtrate increased towards normal whereas the phosphate balance became markedly positive. Most importantly, however, repeat bone biopsies revealed that therapy had positively affected the osteomalacic component of the disease, resulting in normalization of the mineralization front activity. Indeed, a central role for 1,25-dihydroxyvitamin D(3) in the mineralization of the osteomalacic bone is suggested by the linear relationship between the serum level of this active vitamin D metabolite and the mineralization front activity. We, therefore, suggest that a relative deficiency of 1,25-dihydroxyvitamin D(3) is a factor in the pathogenesis of X-linked hypophosphatemic rickets and osteomalacia and may modulate the phenotypic expression of this disease.
尽管肾磷酸盐转运缺陷似乎已被确认为X连锁低磷性佝偻病和骨软化症发病机制的主要潜在异常,但一些观察结果表明,肾磷酸盐流失和低磷血症不能完全解释该疾病特征性异常的范围。因此,在本研究中,我们调查了维生素D代谢异常在该疾病发病机制中的潜在作用,以及1,25 - 二羟基维生素D(3)治疗对该疾病生化异常和骨软化症的影响。4名未经治疗的患者,年龄在14 - 30岁之间,血钙正常(9.22±0.06mg/dl);血磷降低(2.25±0.11mg/dl);每升肾小球滤过液中磷酸盐重吸收的肾小管最大重吸收率降低(2.12±0.09mg/dl);血清免疫反应性甲状旁腺激素浓度正常;磷平衡为负;骨活检有骨软化症证据。血清25 - 羟基维生素D(3)浓度为33.9±7.2ng/ml,尽管存在低磷血症,但1,25 - 二羟基维生素D(3)的血清水平并未升高,而是正常的,为30.3±2.8pg/ml。这些数据表明,维生素D代谢的异常稳态可能是X连锁低磷性佝偻病/骨软化症表型表达的第二个核心缺陷。这一假设得到了对三名受试者进行药理剂量的1,25 - 二羟基维生素D(3)长期治疗反应评估的支持。治疗方案导致血清1,25 - 二羟基维生素D水平升高至超生理范围的值。此外,血清磷酸盐和每升肾小球滤过液中磷酸盐重吸收的肾小管最大重吸收率趋向于正常,而磷平衡变得明显为正。然而,最重要的是,重复骨活检显示治疗对该疾病的骨软化成分产生了积极影响,使矿化前沿活性恢复正常。事实上,这种活性维生素D代谢物的血清水平与矿化前沿活性之间的线性关系表明1,25 - 二羟基维生素D(3)在骨软化骨矿化中起核心作用。因此,我们认为1,25 - 二羟基维生素D(3)相对缺乏是X连锁低磷性佝偻病和骨软化症发病机制中的一个因素,并且可能调节该疾病的表型表达。