Whyte M P, Seino Y
J Clin Endocrinol Metab. 1982 Jul;55(1):178-80. doi: 10.1210/jcem-55-1-178.
25OHD, 1,25,-(OH))2D, and 24,25-(OH)2D were assayed in the serum of 16 patients with the infantile, childhood, or adult form of hypophosphatasia. Except for diminished 1,25-(OH)2D and elevated 24,25-(OH)2D levels in 2 infants (which could be attributed to nonparathyroid hormone-mediated hypercalcemia), the mean circulating level of each vitamin D metabolite was normal in the 3 patient groups. Abnormalities in vitamin D metabolism do not appear to contribute to the pathogenesis of this rare hereditary form of rickets or osteomalacia, which occurs despite normal circulating calcium, inorganic phosphate, and vitamin D metabolite levels.
对16例患有婴儿型、儿童型或成人型低磷酸酯酶症患者的血清进行了25羟维生素D(25OHD)、1,25 - 二羟维生素D(1,25,-(OH))2D)和24,25 - 二羟维生素D(24,25-(OH)2D)检测。除2例婴儿1,25-(OH)2D水平降低和24,25-(OH)2D水平升高(这可能归因于非甲状旁腺激素介导的高钙血症)外,3组患者中每种维生素D代谢物的平均循环水平均正常。维生素D代谢异常似乎与这种罕见的遗传性佝偻病或骨软化症的发病机制无关,尽管循环钙、无机磷和维生素D代谢物水平正常,但仍会发生这种疾病。