Osteoporosis is a highly prevalent disease. More than half of postmenopausa
l women will experience fractures. Women at high risk (osteoporosis as meas
ured by bone density, low trauma fractures of any type, or certain other ri
sk factors) often require pharmacological therapy. However, surveys show th
at most women who have recently had fractures are currently not being treat
ed. Recent results from the first megatrial of osteoporosis with >6400 part
icipants, the Fracture Intervention Trial (FIT), have provided important ad
vances in our understanding of osteoporosis and the efficacy of alendronate
. The FIT study and other large clinical trials show that alendronate effec
tively increases bone density, reduces the risk of hip and vertebral fractu
res by approximately half within the first 12-18 months, and, most importan
tly, reduces the health consequences of fractures. Alendronate is also effe
ctive for preventing bone loss in early postmenopausal women. Thus, alendro
nate represents an important option for preventing and treating this common
and debilitating disease. This article summarizes the wealth of data from
FIT and other studies of alendronate in the context of the burden of illnes
s associated with osteoporosis.