Thomas M K, Demay M B
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Endocrinol Metab Clin North Am. 2000 Sep;29(3):611-27, viii. doi: 10.1016/s0889-8529(05)70153-5.
The disorders of vitamin D metabolism are inherited metabolic abnormalities involving mutations of the vitamin D receptor or enzymes involved in the metabolism of vitamin D to its biologically active form 1,25-dihydroxyvitamin D. Although these mutations are rare, studies in affected patients and animal models have helped to identify critical actions of vitamin D and the mechanism by which it exerts its effects. Vitamin D deficiency, however, is an increasingly recognized problem among the elderly and in the general population. Screening for vitamin D deficiency only in those patients with known risk factors will result in a large proportion of unrecognized affected patients.
维生素D代谢紊乱是遗传性代谢异常,涉及维生素D受体或参与将维生素D代谢为其生物活性形式1,25-二羟基维生素D的酶的突变。尽管这些突变很少见,但对受影响患者和动物模型的研究有助于确定维生素D的关键作用及其发挥作用的机制。然而,维生素D缺乏在老年人和普通人群中是一个日益受到认可的问题。仅对那些有已知风险因素的患者进行维生素D缺乏筛查,将导致很大一部分未被识别的受影响患者。