Clinical Endocrinology · 1982 · 40 citations · 23 references
MedicineEndocrinologyPharmacologyBone MetabolismCalcium HomeostasisMineral MetabolismBone Metabolism DisordersCalcium MetabolismMetabolic Bone DiseaseVitamin DVitamin D DisordersVitamin D MetabolismMineral Metabolism DisordersSerum Calcium MeasurementThyroid Hormone MetabolitesVitamin D MetabolitesVitamin D Physiology
The serum concentrations of 25-hydroxycholecalciferol (25 OH D3), 24,25-dihydroxycholecalciferol [24,25(OH)-2D3] and 1,25-dihydroxycholecalciferol [1,25(OH)2D3] were measured in twenty-one patients with untreated hyperthyroidism. Compared with control subjects, 25 OH D3 concentrations were not altered, 24,25(OH)2D3 concentrations were increased, although not significantly and 1,25(OH)2D3 concentrations were decreased (P = 0.01). Following oral carbimazole therapy, 24,25(OH)2D3 concentrations fell (P less than 0.01), 1,25(OH)2D3 concentrations increased (P less than 0.01) and 25 OH D3 concentrations were unchanged. The altered 1,25(OH)2D3 and 24,25(OH)2D3 concentrations found in hyperthyroidism are probably due to the effects of thyroid hormone on bone and mineral metabolism. Increased serum calcium and phosphate concentrations with secondary hypoparathyroidism result in stimulation of the renal 24-hydroxylase and suppression of the 1-hydroxylase enzymes. In addition, serum 24,25(OH)2D3 concentrations were significantly correlated with serum triiodothyronine levels (T3) (r = 0.66, P less than 0.002) before treatment. This may indicate a direct stimulatory effect of T3 on 24-hydroxylase activity. No relationship was found between serum 1,25(OH)2D3 concentrations before therapy and serum T3.
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Direct stimulation of bone resorption by thyroid hormones.
Gregory R. Mundy, J L Shapiro, Janet G. Bandelin et al. · Journal of Clinical Investigation · 1976 · 382 citations · Full text
Denise Dale · Andrologia · 2009 · 198 citations