Correlations of Serum Concentrations of 1,25-Dihydroxyvitamin D, Phosphorus, and Parathyroid Hormone in Tumoral Calcinosis*
- 1 July 1988
- journal article
- research article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 67 (1) , 88-92
- https://doi.org/10.1210/jcem-67-1-88
Abstract
The inherited metabolic disorder tumoral calcinosis is characterized by elevated serum phosphorus and 1,25- dihydroxyvitamin D [1,25-(OH)2D] levels and paraarticular calcific tumors. The pathogenesis of this disease is obscure, but an elevated renal phosphate reabsorption threshold and increased production of 1,25-(OH)2D are postulated as defects. We studied nine affected patients and found that both serum phosphorus and renal phosphate reabsorption threshold (TmP/GFR) were positively correlated with serum 1,25-(OH)2D levels. Since tumoral calcinosis is a disorder with abnormal renal phosphate transport, we compared the TmP/GFR and serum 1,25-(OH)2D levels to values obtained in patients with two other diseases with renal phosphate transport defects: oncogenic osteomalacia and X-linked hypophosphatemic rickets. We found a significant correlation between TmP/GFR and 1,25-(OH)2D levels in all three diseases, suggesting that in these diseases 1,25-(OH)2D production is regulated in some manner by phosphate transport. Furthermore, previous work indicated that in tumoral calcinosis broad variation exists in serum phosphorus levels. In our patients a negative correlation was found between the serum PTH concentrations and both serum phosphorus levels and TmP/GFR values, respectively. We postulate that although the basic defect in tumoral calcinosis most likely resides in the proximal renal tubular cell, the variation in serum phosphorus levels and possibly disease expression is modulated in part by PTH.Keywords
This publication has 16 references indexed in Scilit:
- Hyperphosphatemic Tumoral CalcinosisAnnals of Internal Medicine, 1982
- The Efficacy of Vitamin D2and Oral Phosphorus Therapy in X-Linked Hypophosphatemic Rickets and Osteomalacia *Journal of Clinical Endocrinology & Metabolism, 1982
- Tumoral calcinosis: Evidence for concurrent defects in renal tubular phosphorus transport and in 1α,25-dihydroxycholecalciferol synthesisCalcified Tissue International, 1980
- Evaluation of a Role for 1,25-Dihydroxyvitamin D3 in the Pathogenesis and Treatment of X-linked Hypophosphatemic Rickets and OsteomalaciaJournal of Clinical Investigation, 1980
- Hypophosphatemic Osteomalacia: Association with Prostatic CarcinomaAnnals of Internal Medicine, 1980
- Phosphorus Excretion in Tumoral Calcinosis: Response to Parathyroid Hormone and Acetazolamide*Journal of Clinical Endocrinology & Metabolism, 1980
- Calcium and Phosphate Metabolism in Tumoral CalcinosisAnnals of Internal Medicine, 1980
- Osteomalacia Due to 1α,25-Dihydroxycholecalciferol DeficiencyJournal of Clinical Investigation, 1977
- Tumoral calcinosisThe American Journal of Medicine, 1965
- THE DETERMINATION OF CREATINE AND CREATININE IN URINE - A CORRECTION FACTOR FOR THE DETERMINATION OF 24-HOUR URINARY EXCRETION VALUES1954