Osteoporosis is the most important metabolic bone disease and places a
n increasing burden on the healthcare system. The condition can be pre
vented by the early introduction of hormone replacement therapy. The r
ole of bisphosphonates in achieving the same result is being actively
explored. The attraction of preventing bone loss is that it preserves
the micro-architecture of bone, and therefore its mechanical integrity
. The great problem of treating the established condition is that subs
tantial bone loss is accompanied by architectural disintegration. Repl
acing lost bone may not necessarily restore mechanical integrity and p
rotect against fractures. The management of Paget's disease has been q
uite revolutionised by the introduction of the bisphosphonates. The co
ndition is a result of a primary increase in osteoclastic bone resorpt
ion which can be corrected by bisphosphonates, with considerable sympt
omatic improvement. The increasing potency and safety margin of the ne
wer agents has meant that the threshold for treatment has fallen. Ther
e is now potential for long term control of bone turnover with the hop
e of preventing late complications. Hypercalcaemia of malignancy is us
ually the result of both increased bone destruction and decreased urin
ary calcium excretion. These two components of hypercalcaemia demand d
ifferent approaches to management. The general availability of an ever
-expanding range of increasingly potent bisphosphonates has resulted i
n a dramatic improvement in the treatment of increased bone resorption
associated with malignancy. Many types of tumour, either directly or
indirectly, compromise the ability of the kidney to eliminate a calciu
m load derived from increased bone destruction. Calcitonin is the only
agent which is currently available to counter this process.