Parathyroid hormone independent hypercalcemia in adults

Best Pract Res Clin Endocrinol Metab. 2018 Oct;32(5):621-638. doi: 10.1016/j.beem.2018.06.005. Epub 2018 Jun 18.

Abstract

Parathyroid independent hypercalcemia is characterized by suppressed parathyroid hormone (PTH) in the presence of hypercalcemia. Well known causes and mechanisms are redistribution of calcium from the skeleton, by malignant diseases; inadequately increased intestinal calcium uptake mediated by increased vitamin D activity, and reduced renal elimination due to medications. Frequent and infrequent causes are discussed, and more recent mechanistic models presented in this review. Most hypercalcemic conditions are stable and in equilibrium between the different organs, whereas the utmost severe cases are characterized by rapid rising calcium levels and renal failure, resulting in a vicious circle where a disequilibrium state is developed. Management and treatment depends on the underlying condition and severity. The aim of this review is to discuss non-parathyroid hypercalcemic conditions as seen in the modern clinic, with a focus on areas where recent gain of knowledge has been achieved.

Keywords: PTHR1 (Parathyroid hormone 1 receptor); PTHrP (PTH-related peptide); Vitamin D; immobilization; sarcoidosis.

Publication types

  • Review

MeSH terms

  • Adult
  • Calcium / blood
  • Humans
  • Hypercalcemia* / diagnosis
  • Hypercalcemia* / epidemiology
  • Hypercalcemia* / etiology
  • Hypercalcemia* / therapy
  • Parathyroid Hormone / blood*
  • Parathyroid Hormone / physiology
  • Parathyroid Hormone-Related Protein / blood

Substances

  • Parathyroid Hormone
  • Parathyroid Hormone-Related Protein
  • Calcium