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Different vitamin D substrate-product relationship after oral vitamin D supplementation in familial benign hypercalcemia, primary hyperparathyroidism, and healthy controls.

AbstractCONTEXT:
In healthy subjects and in patients with primary hyperparathyroidism (PH), the administration of a low dose of 25(OH)D (25 μg/day) increases the serum levels of both 25(OH)D and 1,25(OH)(2)D. It is unknown whether this relationship is present in patients affected by familial benign hypocalciuric hypercalcemia (FBH).
OBJECTIVE:
To evaluate the different vitamin D substrate-product relationship after oral vitamin D supplementation in familial benign hypercalcemia, PH, and healthy controls.
DESIGN:
We evaluated the main physiological regulators of 1α-hydroxylase and the substrate-product relationship of 25(OH)D and 1,25(OH)(2)D in 20 patients with PH, 25 with FBH, and 122 healthy sex- and age-matched controls before and after administration of 25(OH)D for 2 weeks.
RESULTS:
25(OH)D increased significantly in all subjects, whereas 1,25(OH)(2)D serum levels increased significantly in PH patients and healthy controls but not in patients with FBH. Therefore, a significant positive substrate-product relationship of 25(OH)D-1,25(OH)(2)D was found in PH and healthy controls, but not in FBH. Monomeric calcitonin (hCT-M) was significantly lower at baseline and after 25(OH)D supplementation in the FBH group compared with the other two groups.
CONCLUSIONS:
The lack of 1,25(OH)(2)D increase in FBH may be due to a direct inhibitory effect on 1α-hydroxylase of hypercalcemia per se, increased metabolic clearance of 1,25(OH)(2)D, or a decreased stimulus of 1α-hydroxylase related to persistently low levels of hCT.
AuthorsMaurizio Bevilacqua, Marco Invernizzi, Velella Righini, Stefano Carda, Carlo Cisari
JournalEuropean journal of endocrinology (Eur J Endocrinol) Vol. 164 Issue 5 Pg. 833-8 (May 2011) ISSN: 1479-683X [Electronic] England
PMID21310873 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Vitamin D
Topics
  • Administration, Oral
  • Aged
  • Dietary Supplements
  • Female
  • Humans
  • Hypercalcemia (blood, congenital, drug therapy)
  • Hyperparathyroidism, Primary (blood, drug therapy)
  • Male
  • Middle Aged
  • Substrate Specificity
  • Vitamin D (administration & dosage, blood)

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