This study investigated whether bone turnover influences the response to al
endronate in women with postmenopausal osteoporosis. One hundred postmenopa
usal osteoporotic women were randomized to receive either alendronate (10 m
g/day) plus calcium (1000 mg/day) (n = 50) or calcium alone (n = 50). Verte
bral and radial bone density, measured by DXA, and markers of bone turnover
were assessed at baseline and after 1 and 2 years. At the end of treatment
, alendronate users showed an increase of 5.0% and 2.3%, respectively, at t
he lumbar spine and ultradistal radius; in the group treated only with calc
ium, bone mineral density (BMD) decreased by 1.6% at the lumbar spine and 1
.3% at the ultradistal radius. The difference between the two groups was si
gnificant (P < 0.001). The patients were divided into high (HT) or low (LT)
bone turnover groups, as assessed by 24-hour whole body retention (WBR%) o
f Tc-99m-methylene-diphosphonate. The response to alendronate treatment was
greater in HT patients compared with LT patients. In fact, at the end of t
he study period, BMD at the lumbar spine had increased by 7.9% in HT patien
ts and by 3.0% in LT patients; the difference between the two groups was si
gnificant (P < 0.001). No significant difference between the two groups was
found for BMD at the ultradistal radius. In conclusion, the present study
demonstrates that 2-year treatment with alendronate has highly positive eff
ects on bone mass at both the lumbar spine and ultradistal radius. The incr
ease in bone mass, especially at the axial level, is influenced by bone tur
nover. Therefore, the evaluation of bone turnover may be useful in predicti
ng the response to alendronate treatment.