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X连锁低磷性佝偻病和骨软化症患者的血清1,25-二羟基维生素D水平。

Serum 1,25-dihydroxyvitamin D levels in subjects with X-linked hypophosphatemic rickets and osteomalacia.

作者信息

Lyles K W, Clark A G, Drezner M K

出版信息

Calcif Tissue Int. 1982 Mar;34(2):125-30. doi: 10.1007/BF02411222.

Abstract

In order to determine whether a defect in vitamin D metabolism might play a role in the pathogenesis of X-linked hypophosphatemic rickets and osteomalacia (XLH), we compared the serum 1,25-dihydroxyvitamin D [1,25(OH)2D] level in 52 normal subjects and 37 patients with XLH. In untreated patients, adults were found to have values similar to age-matched controls, while youths had values similar to growth-rate-matched controls but significantly lower than the levels of age-matched controls who were growing at a normal rate. In contrast, treated XLH patients of all ages had serum levels significantly lower than both controls and untreated XLH patients. Further, the serum levels of 1,25(OH)2D in these treated patients had a significant inverse linear correlation with serum 25-(OH)D concentrations. We propose that subjects with XLH have serum 1,25(OH)2D levels within appropriate age- and growth-rate-matched normal ranges. However, in the presence of hypophosphatemia, we would have anticipated elevated levels of 1,25(OH)2D; viewed in this light the serum 1,25(OH)2D levels are inadequate, suggesting the presence of a relative deficiency of this active vitamin D metabolite.

摘要

为了确定维生素D代谢缺陷是否可能在X连锁低磷性佝偻病和骨软化症(XLH)的发病机制中起作用,我们比较了52名正常受试者和37名XLH患者的血清1,25-二羟维生素D [1,25(OH)2D]水平。在未经治疗的患者中,发现成年人的值与年龄匹配的对照组相似,而青少年的值与生长速率匹配的对照组相似,但显著低于正常生长速率的年龄匹配对照组的水平。相比之下,所有年龄段的经治疗的XLH患者的血清水平均显著低于对照组和未经治疗的XLH患者。此外,这些经治疗患者的血清1,25(OH)2D水平与血清25-(OH)D浓度呈显著的负线性相关。我们提出,XLH患者的血清1,25(OH)2D水平在适当的年龄和生长速率匹配的正常范围内。然而,在存在低磷血症的情况下,我们本应预期1,25(OH)2D水平会升高;从这个角度来看,血清1,25(OH)2D水平不足,表明存在这种活性维生素D代谢物的相对缺乏。

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