Calcitonin, a polypeptide hormone secreted by the parafollicular C cel
ls of the thyroid gland, lowers serum calcium by decreasing bone resor
ption and tubular calcium reabsorption. An analgesic action, possibly
mediated via beta-endorphins, is also evident. Parenteral calcitonin h
as been shown to stabilise and increase indices of cortical and trabec
ular bone mass and total body calcium when administered to patients wi
th established osteoporosis. The routine use of this route of administ
ration has been limited by poor patient compliance and tolerability. A
n intranasal preparation of calcitonin provided a more convenient mean
s of administration. Several clinical trials have shown that intranasa
l calcitonin is effective and well tolerated both in prevention of pos
tmenopausal bone loss and in established osteoporosis. Calcitonin ther
apy is particularly indicated for patients with high-turnover osteopor
osis where results show a net gain of bone mineral in the axial skelet
on and a slowing of bone loss in the appendicular bones. Due to recept
or downregulation a resistance to the hormone may occur after 12-18 mo
nths of continuous treatment. This resistance can be avoided and delay
ed by the cyclical or discontinued administration of the hormone. Furt
her research is needed to confirm longer-term efficacy and effects on
fracture rate.