Elevations in serum and urinary calcium with parathyroid hormone (1-84) with and without alendronate for osteoporosis

Diana M. Antoniucci, Deborah E. Sellmeyer, John P. Bilezikian, Lisa Palermo, Kristine E. Ensrud, Susan L. Greenspan, Dennis M. Black

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Context: The effect of PTH therapy on serum and urinary calcium levels and the risk of hypercalcemia or hypercalciuria has not been formally evaluated. Objective: The objective was to examine changes in serum and urinary calcium associated with PTH(1-84) therapy in the PaTH trial and the extent to which a defined algorithm resolved the elevated values. Design, Setting, Participants, and Intervention: A total of 178 postmenopausal women were randomized to PTH(1-84) either alone or in combination with alendronate during the first year of the PaTH study. Main Outcome Measure(s): The main outcome measures were fasting serum calcium at baseline and 1, 3, and 12 months and 24-h urinary calcium at baseline and 3 months. Results: In 14% of participants, serum calcium more than 10.5 mg/dl (>2.6 mmol/liter) developed. Following the defined algorithm, 58% of elevated measurements were normal on repeat testing; 38% required discontinuation of calcium and vitamin D supplementation, and one necessitated a decrease in PTH injection frequency to normalize serum calcium. One participant developed transient hypercalcemia between study visits and required hospitalization; the episode resolved with iv hydration and PTH discontinuation. Baseline characteristics associated with the development of hypercalcemia were serum calcium [relative hazards = 1.9 per 0.5 mg/dl (0.12 mmol/liter); 95% confidence interval = 1.1-3.2] and serum 1,25-dihydroxyvitamin D [relative hazard = 1.9 per 10 pg/ml (26 pmol/liter); 95% confidence interval = 1.2-3.1]. Fifteen women (8%) developed hypercalciuria [urinary calcium > 400 mg (100 mmol)/24 h or calcium/creatinine ratio > 0.4]; 80% of cases resolved after discontinuing calcium and vitamin D, 13% without intervention, and one after PTH injection frequency was decreased. Higher baseline urinary calcium excretion was associated with development of hypercalciuria [relative hazard = 1.5 per 50 mg/d (12.5 mmol/d); 95% confidence interval = 1.2-4.0]. Proportions of patients with elevated serum and urinary calcium were similar on single and combination therapy. Conclusions: The frequency of episodic hypercalcemia or hypercalciuria in the PaTH trial was 21%. Episodes were generally mild, and nearly all cases resolved spontaneously or with discontinuation of calcium and vitamin D. The algorithms used to address hypercalcemia and hypercalciuria in the PaTH trial proved effective in safely resolving clinical episodes of increased urinary or serum calcium and might therefore be helpful to clinicians caring for patients on PTH.

Original languageEnglish (US)
Pages (from-to)942-947
Number of pages6
JournalJournal of Clinical Endocrinology and Metabolism
Volume92
Issue number3
DOIs
StatePublished - Mar 2007

Bibliographical note

Funding Information:
This work was supported by a contract (NIAMS-045, N01-AR-9-2245) with the National Institutes of Arthritis and Musculoskeletal and Skin Disorders (to D.M.B.). Funding for this project was from NPS Pharmaceuticals (to D.M.A. and D.M.B.) and the Veterans Affairs Research Enhancement Award Program (to D.M.A.).

Funding Information:
Disclosure Statement: L.P. and K.E.E. have nothing to declare. D.M.A. has received grant support from NPS (08/05 to 06/06). D.E.S. has received lecture fees from Merck. J.P.B. consults for and has received lecture fees from Lilly and Merck. S.L.G. consults for and has received lecture fees from Merck and Allelix. S.L.G. has also received grant support from NPS Allelix (2000-2005) and Merck (2002-2005). D.M.B. consults for NPS and receives lecture fees from Merck.

Fingerprint

Dive into the research topics of 'Elevations in serum and urinary calcium with parathyroid hormone (1-84) with and without alendronate for osteoporosis'. Together they form a unique fingerprint.

Cite this