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Title: Strontium and calcium metabolism in metabolis bone diseases

Journal Article · · Journal of Clinical Investigation
DOI:https://doi.org/10.1172/JCI104109· OSTI ID:4156545

The distribution and excretion of Sr85 and Ca45 administered simultaneously and intravenously were studied in patients with thyroid and parathyroid disorders, osteoporosis, and Paget's disease. In all cases and at all times the body retention of Ca45 was more than Sr85 retention by a factor of 1.1 to 5.7. Differential renal clearance of the two isotopes accounted for 1.9 to 8.1 times more Sr85 than Ca45 in the urine. The amounts of each isotope in the feces were sizable, generally equal, and varied little in the different diseases studied, except in Paget' s disease. Calcium pools and compartment sizes as determined by either isotope proved to be sensitive indices of skeletal function. The largest values were found in Paget's disease and thyrotoxicosis and the lowest in myxedema. One patient with thyroid cancer metastatic to bone showed no evidence of increased calcium turnover by any of the criteria employed. A patient with hyperparathyroidism but no clinical evidence of bone disease showed no evidence of abnormal calcium or strontium dynamics. In one patient with Paget's disease cortisone failed to suppress completely the activity of the disease as measured by Ca45 dynamics. There was no unusual pattern of labeled isotope excretion in patients with osteoporosis. Prolonged estrogen therapy in one patient with osteoporosis of the postmenopausal type effected no change in skeletal kinetics as measured by the metabolism of Ca45 or Sr85 but did effect a change in the serum to urine Ca45 specific activity ratio. The observation that Ca45 specific activities were consistently greater in serum than in urine and the variation of serum to urine ratios in different disease states is discussed as representing either a true phenomenon or a systematic analytical error. Strontium-85 qualitatively parallels Ca45 as an index of skeletal function in metabolic bone diseases.

Research Organization:
Massachusetts General Hospital, Boston, MA (United States); Harvard Medical School, Boston, MA (United States)
Sponsoring Organization:
USDOE
NSA Number:
NSA-14-015503
OSTI ID:
4156545
Journal Information:
Journal of Clinical Investigation, Vol. 39, Issue 6; Other Information: Orig. Receipt Date: 31-DEC-60; ISSN 0021-9738
Country of Publication:
Country unknown/Code not available
Language:
English