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. 1979 Mar 13;27(1):13-8.
doi: 10.1007/BF02441155.

Anticonvulsant drug-induced osteomalacia: alterations in mineral metabolism and response to vitamin D3 administration

Anticonvulsant drug-induced osteomalacia: alterations in mineral metabolism and response to vitamin D3 administration

T J Hahn et al. Calcif Tissue Int. .

Abstract

Parameters of mineral metabolism were examined in 6 patients with moderately severe anticonvulsant drug-induced osteomalacia. Compared to 15 matched controls, the patients exhibited significantly reduced serum calcium, inorganic phosphate, and 25-hydroxyvitamin D concentration, elevated serum alkaline phosphatase and immunoreactive parathyroid hormone (iPTH) concentration, reduced intestinal 47Ca absorption, reduced urinary calcium and increased urinary hydroxyproline excretion, and reduced forearm bone mass. Intestinal absorption of vitamin D3 was normal. Following 4 months of treatment with vitamin D3 (4000 units/day), serum 25-OHD concentration was increased to 3 times mean normal values and all parameters except serum iPTH, urinary calcium excretion, and forearm bone mass were returned to levels not significantly different from normal. Serum iPTH concentration was reduced by 39% (P less than 0.05); 24-h urinary calcium excretion rose by 98% (P less than 0.001), and forearm bone mass increased by 5.6% (P less than 0.05). It is concluded that moderate-dose vitamin D3 supplementation is effective in normalizing parameters of mineral metabolism in this disorder, despite evidence of resistance to the biologic effects of vitamin D.

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References

    1. J Clin Endocrinol Metab. 1975 Nov;41(5):926-37 - PubMed
    1. Drugs. 1976;12(3):201-11 - PubMed
    1. Arch Dis Child. 1974 May;49(5):344-50 - PubMed
    1. Proc Soc Exp Biol Med. 1976 Nov;153(2):220-4 - PubMed
    1. J Clin Endocrinol Metab. 1974 Aug;39(2):274-82 - PubMed

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