Failure of cimetidine to affect calcium homeostasis in familial primary hyperparathyroidism (multiple endocrine neoplasia, type 1)

J Clin Endocrinol Metab. 1980 Oct;51(4):912-4. doi: 10.1210/jcem-51-4-912.

Abstract

Recent reports that cimetidine, a blocker of histamine H2 receptors, lowered serum calcium and/or immunoreactive parathyroid hormone (PTH) concentrations in primary or secondary hyperparathyroidism prompted us to administer the drug (300 mg, orally, every 6 h) to two patients with hyperparathyroidism accompanying familial multiple endocrine neoplasia type 1. The patients were hypercalcemic (10.9--11.2 mg/dl), hypophosphatemic (2.0--2.4 mg/dl), and hypercalciuric (greater than or equal to 410 mg/24 h), with elevated urinary cAMP and phosphate clearance and inappropriately high serum immunoreactive PTH levels. Multiple observations of these variables over 5 weeks of cimetidine treatment showed no systematic changes; in particular, serum and urinary calcium did not change, and there was no evidence of a decreased PTH effect on the kidneys. The data offer no support for the treatment of familial hyperparathyroidism with cimetidine.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Calcium / metabolism*
  • Cimetidine / therapeutic use*
  • Creatinine / metabolism
  • Female
  • Guanidines / therapeutic use*
  • Homeostasis
  • Humans
  • Hyperparathyroidism / drug therapy*
  • Hyperparathyroidism / genetics
  • Hyperparathyroidism / metabolism
  • Male
  • Middle Aged
  • Multiple Endocrine Neoplasia / drug therapy
  • Multiple Endocrine Neoplasia / metabolism
  • Parathyroid Hormone / blood
  • Phosphorus / metabolism

Substances

  • Guanidines
  • Parathyroid Hormone
  • Phosphorus
  • Cimetidine
  • Creatinine
  • Calcium