1,25-dihydroxy vitamin D production in response to two successive infusions of synthetic active 1-34 fragment of human PTH [hPTH-(l-34)] was evaluated in order to develop an understanding of the vitamin D metabolism and the rationale of vitamin D therapy in calcium disorders. Five normal controls, six hypoparathyroid patients, two patients with hypophosphatemic vitamin-D-resistant rickets, one patient with Lowe's synd. and one patient with primary Fanconi's synd. were investigated, and the following results were obtained. All normal controls showed a significant increase in serum 1,25(OH)2D[43± 3.8 (m±SEM, n=5, basal), 53±4.3 (three hours after the first PTH infusion), 65 ±7.7 (six hours) and 66 ±4.4 (nine hours) pg/ml]. All patients with PTH-deficient hypoparathyroidism showed a significant increase in serum 1,25(OH)2D, and serum 1,25(OH)2D values were within the normal range after hPTH-(1-34) stimulation. Serum 1,25(OH)2D remained low after hPTH-(1-34) infusions in a patient with pseudohypoparathyroidism type I who showed a significant increase in this value after infusion of dibutyryl cyclic AMP. On the other hand, a patient with normocalcemic pseudohypoparathyroidism type I had a high basal 1,25(OH)2D value, which increased further after hPTH-(1-34) infusions. An almost normal increase in serum 1,25(OH)2D was observed in two patients with hypophosphatemic vitamin-D-resistant rickets, one with Lowe's syndrome and the other with primary Franconi's syndrome. We conclude that these results are important in obtaining an understanding of calcium and vitamin D metabolism in these disorders and that this PTH stimulation test is a useful method to use in evaluating renal responsiveness in 1,25(OH)2D production to PTH in various calcium disorders. © 1984, The Japan Endocrine Society. All rights reserved.
CITATION STYLE
Yasuda, T., & Nakajima, H. (1984). 1,25-Dihydroxyvitamin D Production after Stimulation with Synthetic Human Parathyroid Hormone (1-34) in Hypoparathyroid and Renal Tubular Disorders. Endocrinologia Japonica, 31(4), 407–415. https://doi.org/10.1507/endocrj1954.31.407
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