D. Thiebaud et al., 2 YEARS EFFECTIVENESS OF INTRAVENOUS PAMIDRONATE (APD) VERSUS ORAL FLUORIDE FOR OSTEOPOROSIS OCCURRING IN THE POSTMENOPAUSE, Osteoporosis international, 4(2), 1994, pp. 76-83
Bisphosphonates seem to be effective as antiresorptive agents in the p
revention and treatment of osteoporosis. However, the optimal dose and
route of administration as well as the specific effects on cortical o
r trabecular bone have not been clarified. To compare pamidronate (APD
) with fluoride (F) in the therapy of postmenopausal osteoporosis, 32
osteoporotic women were treated for 2 years either with APD (30 mg as
a single intravenous infusion over 1 h every 3 months, n = 16, mean ag
e 65 years) or with fluoride orally (20-30 mg F/day, n = 16, mean age
67 years) in an open study. Both groups received 1 g calcium and 1000
U vitamin D per day, but no estrogens or other drugs acting on bone. B
oth groups showed the same initial mean number of fractures per patien
t (2.8 and 2.7). Bone densitometry was performed every 6 months at thr
ee sites: lumbar spine and hip with dual-energy X-ray absorptiometry (
BMD), distal forearm with single photon absorptiometry and lumbar spin
e with quantitative computed tomography. Biochemical assessment was pe
rformed in blood and urine every 3 months. Lumbar BMD (g/cm2, mean +/-
SEM) increased from 0.632 (+/- 0.030) at time 0 to 0.696 (+/- 0.028)
at 24 months in the APD group (p < 0.001), and from 0.684 (+/- 0.025)
to 0.769 (+/- 0.028) in the fluoride group (p < 0.001). Femoral neck B
MD increased significantly from 0.558 (+/- 0.025) to 0.585 (+/- 0.025)
(p < 0.01) in the APD group, whereas it did not change in the fluorid
e group. Forearm SPA (g/cm) increased from 0.90 (+/- 0.08) to 0.97 (+/
- 0.10) (p < 0.01) in the APD group, whereas it decreased from 0.94 +/
- (0.06) to 0.90 (+/- 0.06) (p < 0.05) in the fluoride group. Plasma c
alcium, parathormone and creatinine did not change in any group. Urina
ry hydroxyproline/creatinine, serum osteocalcin and alkaline phosphata
se decreased significantly with APD, but did not change with fluoride,
except for an increase in osteocalcin. Two new vertebral fractures oc
curred with APD and 6 with fluoride, plus 1 hip fracture. Side effects
were a transient fever with flu-like symptoms in 5 patients after the
first infusion of APD, rigors and mild phlebitis in 1 patient. Fluori
de was associated with 5 transient arthralgias and 4 mild gastric into
lerances, and treatment was interrupted in 2 patients with distal stre
ss fractures. While fluoride increased only lumbar BMD, intermittent i
ntravenous APD increased lumbar, hip and radial BMD in postmenopausal
osteoporosis and was well tolerated.