Stanbury S W
Contrib Nephrol. 1978;13:132-46. doi: 10.1159/000402141.
Intestinal malabsorption of calcium and the development of osteomalacia in conservatively treated renal failure is explained by a quantitative deficiency of 1,25-dihydroxycholecalciferol, which also contributes to the development of hypocalcaemia. Excess of 25-hydroxycholecalciferol can substitute for this deficiency. The presence and healing of azotaemic osteomalacia is unrelated to the prevailing plasma [Ca] x [P] product. The data suggest that "vitamin D" acts directly on bone mineralisation, but the claim that this apparent effect is normally due to 25-hydroxycholecalciferol is considered unproven. Most of the phenomena of azotaemic osteodystrophy are encountered in simple vitamin D deficiency; as in that condition, deficiency of 1,25-dihydroxycholecalciferol may be of primary significance in causing secondary hyperparathyroidism in renal failure.
在保守治疗的肾衰竭中,肠道对钙的吸收不良及骨软化症的发生是由1,25 - 二羟胆钙化醇的定量缺乏所解释的,这也导致了低钙血症的发生。过量的25 - 羟胆钙化醇可以替代这种缺乏。氮质血症性骨软化症的存在和愈合与当时的血浆[钙]×[磷]乘积无关。数据表明“维生素D”直接作用于骨矿化,但认为这种明显作用通常是由于25 - 羟胆钙化醇所致的说法尚未得到证实。氮质血症性骨营养不良的大多数现象在单纯维生素D缺乏时也会出现;与那种情况一样,1,25 - 二羟胆钙化醇缺乏在肾衰竭导致继发性甲状旁腺功能亢进中可能具有主要意义。