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Treatment of osteomalacia associated with primary biliary cirrhosis with parenteral vitamin D2 or oral 25-hydroxyvitamin D3.

机译:肠胃外维生素D2或口服25-羟基维生素D3治疗与原发性胆汁性肝硬化相关的骨软化症。

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摘要

The histological and biochemical response of osteomalacia has been studied in four patients with primary biliary cirrhosis, who were treated with oral 25-hydroxyvitamin D3, 50 microgram daily, or intramuscular vitamin D2, 150,000 units once weekly, for five to 12 months. All patients showed complete histological healing of osteomalacia, despite rapidly deteriorating liver function in three. Plasma 25-hydroxyvitamin D concentrations were low in all patients before treatment, but became normal during either vitamin therapy. Serum calcium and phosphate levels, and urinary calcium excretion were not always reliable in predicting the histological response to treatment. Serum alkaline phosphatase activity decreased in all patients during vitamin D therapy. We conclude that both high-dose parenteral vitamin D2 and oral 25-hydroxyvitamin D3 may be effective in healing osteomalacia associated with primary biliary cirrhosis. Measurement of plasma 25-hydroxyvitamin D levels during vitamin D therapy provides useful information about 25-hydroxylation of the parent vitamin and intestinal absorption of orally administered 25-hydroxyvitamin D3.
机译:在四名原发性胆汁性肝硬化患者中研究了骨软化症的组织学和生化反应,他们接受口服口服25-羟基维生素D3(每天50微克)或肌肉内维生素D2(每周一次150,000单位)治疗,持续5至12个月。尽管三分之二的肝功能迅速恶化,所有患者均显示出骨软化症的完整组织学愈合。治疗前所有患者的血浆25-羟基维生素D浓度均较低,但在任一维生素治疗期间均恢复正常。血清钙和磷酸盐水平以及尿钙排泄在预测对治疗的组织学反应方面并不总是可靠的。维生素D治疗期间所有患者的血清碱性磷酸酶活性均下降。我们得出的结论是,大剂量肠胃外维生素D2和口服25-羟基维生素D3均可有效治愈与原发性胆汁性肝硬化相关的骨软化症。维生素D治疗期间血浆25-羟基维生素D水平的测量提供了有关母体维生素25-羟基化和口服25-羟基维生素D3肠道吸收的有用信息。

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