Objective. To examine the clinical implications of disturbed calcium metabo
lism in sarcoidosis and how the pathophysiology affects management strategi
es.
Methods. The literature concerning calcium metabolism in sarcoidosis was re
viewed.
Results. Dysregulated calcium metabolism is a well-recognized complication
of sarcoidosis, resulting in hypercalcaemia (prevalence 5-10%), hypercalcur
ia (40-62%) and reduced bone density (40-55%). Extrarenal synthesis of calc
itriol [1,25(OH)(2)D-3] is central to the pathogenesis of abnormal calcium
homeostasis, but alterations in parathyroid hormone (PTH) activity and the
expression of PTH-related peptide have also been demonstrated. The immunosu
ppressive properties of calcitriol suggest that the raised levels seen in s
arcoidosis could represent an adaptive response to the undefined antigen th
at causes sarcoidosis.
Conclusions. The mechanisms of abnormal calcium metabolism in sarcoidosis n
eed to be understood when treating hypercalcaemia, hypercalcuria and cortic
osteroid-induced osteoporosis. Studies are required to determine if the cur
rently available therapies for osteoporosis are safe and effective in sarco
idosis.