RECOVERY OF PARATHYROID-HORMONE SECRETION DURING CORRECTION OF TUMOR-ASSOCIATED HYPERCALCEMIA

被引:10
作者
BODY, JJ [1 ]
DUMON, JC [1 ]
SERAJ, F [1 ]
CLEEREN, A [1 ]
机构
[1] UNIV LIBRE BRUXELLES, INST JULES BORDET,CTR TUMEURS, LAB INVEST CLIN HJ TAGNON,LAB JC HEUSON, B-1000 BRUSSELS, BELGIUM
关键词
D O I
10.1210/jc.74.6.1385
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Spontaneous recovery of parathyroid secretion during correction of tumor-associated hypercalcemia by bisphosphonates provides a unique clinical opportunity to further unravel the complex relationship between Ca and PTH levels. We measured plasma ionised Ca (Ca2+) and serum intact PTH concentrations in 31 hypercalcemic cancer patients every 2 (range, 1-3) days over a period of 3-21 (median, 7) days after pamidronate therapy. The mean (+/-SD) initial Ca2+ concentration was 1.64 +/- 0.20 mmol/L (normal, 1.05-1.26 mmol/L), with a corresponding PTH level of 4.9 +/- 2.6 (median, 4.5; range, <2.0-14.7) ng/L. PTH levels were subnormal in 30 of 31 patients. During correction of hypercalcemia, the relationship between Ca2+ and PTH concentrations was best described by a polynomial regression (r = 0.89; P < 0,001). The curve of the regression entered the normal range of PTH levels (10.5 ng/L) for a Ca2+ concentration of 1.21 mmol/L. Similarly, the mean Ca2+ level that caused a reproducible increase in PTH levels compared to. baseline values was 1.21 +/- 0.12 (median, 1.17; range, 1.00-1.45) mmol/L. Comparable values were obtained when day to day variations in PTH levels were considered; the mean Ca2+ threshold level was 1.24 +/- 0.12 (median, 1.25; range, 1.00-1.43) mmol/L. This PTH secretory threshold was not significantly influenced by several factors, including the type of cancer hypercalcemia, the day to day variations in Ca2+ levels, various biochemical parameters of calcium metabolism, or the number of days to obtain a normal Ca2+ concentration. In summary, contrary to previous reports, our data show that the PTH secretory threshold during correction of tumor-associated hypercalcemia lies in the upper part of the normal range of Ca2+ concentrations and is not significantly influenced by the rate of change in Ca2+ levels.
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页码:1385 / 1388
页数:4
相关论文
共 19 条
[1]  
Body J J, 1986, J Bone Miner Res, V1, P523
[2]  
BODY JJ, 1989, J BONE MINER RES, V4, P923
[3]   TREATMENT OF MALIGNANCY-ASSOCIATED HYPERCALCEMIA WITH INTRAVENOUS AMINOHYDROXYPROPYLIDENE DIPHOSPHONATE [J].
BODY, JJ ;
BORKOWSKI, A ;
CLEEREN, A ;
BIJVOET, OLM .
JOURNAL OF CLINICAL ONCOLOGY, 1986, 4 (08) :1177-1183
[4]   EPINEPHRINE IS A HYPOPHOSPHATEMIC HORMONE IN MAN - PHYSIOLOGICAL-EFFECTS OF CIRCULATING EPINEPHRINE ON PLASMA CALCIUM, MAGNESIUM, PHOSPHORUS, PARATHYROID-HORMONE, AND CALCITONIN [J].
BODY, JJ ;
CRYER, PE ;
OFFORD, KP ;
HEATH, H .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (03) :572-578
[5]   RECOVERY OF PARATHYROID-HORMONE SECRETION AFTER PARATHYROID ADENOMECTOMY [J].
BRASIER, AR ;
WANG, CA ;
NUSSBAUM, SR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (03) :495-500
[6]   RELATIONSHIP BETWEEN THE CONCENTRATION AND RATE OF CHANGE OF CALCIUM AND SERUM INTACT PARATHYROID-HORMONE LEVELS IN NORMAL HUMANS [J].
BRENT, GA ;
LEBOFF, MS ;
SEELY, EW ;
CONLIN, PR ;
BROWN, EM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 67 (05) :944-950
[7]   HYSTERESIS IN THE RELATIONSHIP BETWEEN SERUM IONIZED CALCIUM AND INTACT PARATHYROID-HORMONE DURING RECOVERY FROM INDUCED HYPERCALCEMIA AND HYPOCALCEMIA IN NORMAL HUMANS [J].
CONLIN, PR ;
FAJTOVA, VT ;
MORTENSEN, RM ;
LEBOFF, MS ;
BROWN, EM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 69 (03) :593-599
[8]   REGULATION OF PARATHYROID-HORMONE SECRETION INVITRO AND INVIVO [J].
FISCHER, JA ;
BLUM, JW ;
BORN, W ;
DAMBACHER, MA ;
DEMPSTER, DW .
CALCIFIED TISSUE INTERNATIONAL, 1982, 34 (04) :313-316
[9]  
GARDIN JP, 1988, MINER ELECTROL METAB, V14, P221
[10]   RATE AND CONCENTRATION-DEPENDENCE OF PARATHYROID-HORMONE DYNAMICS DURING STEPWISE CHANGES IN SERUM IONIZED CALCIUM IN NORMAL HUMANS [J].
GRANT, FD ;
CONLIN, PR ;
BROWN, EM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 71 (02) :370-378