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Treatment of vertebral osteoporosis with disodium monofluorophosphate: Comparison with sodium fluoride
Author(s) -
Delmas P. D.,
Dupuis J.,
Duboeuf F.,
Chapuy M. C.,
Meunier P. J.
Publication year - 1990
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650051322
Subject(s) - fluoride , sodium fluoride , stress fractures , medicine , osteoporosis , bone mineral , dentistry , calcium , bioavailability , urology , chemistry , surgery , pharmacology , inorganic chemistry
Eighty one women with vertebral osteoporosis were treated for up to 2 years with fluoride administered either as monofluorophosphate (MFP, 200 mg/day, i.e., 26.4 mg fluoride‐ion) or sodium fluoride (NaF, 50 mg/day, i.e., 22.6 mg fluoride‐ion). All patients received calcium supplementation (1 g of Ca 2+ /day) taken apart from NaF and in the same tablet for MFP. Despite almost similar fluoride dosage of both regimens, the early increase in the bone mineral density (BMD) of the lumbar spine was higher with MFP than with NaF, reaching 11% and 4%, respectively, at 1 year ( p = 0.007), and 21% and 6%, respectively, at 18 months ( p < 0.001). The incidence of lower extremity pain syndrome related to benign stress microfactures was also higher with MFP than with NaF (35% and 15%, respectively, p < 0.01). Urinary fluoride levels were higher in the MFP than in the NaF group (9.6 ± 3.5 vs. 6.8 ± 3.4 at one year, p = 0.003), suggesting that this difference in efficacy and tolerance is related to a better bioavailability of fluoride provided by MFP than by NaF. The occurrence of a stress microfracture could not be predicted by any clinical, biochemical, or densitometric parameter before treatment, but patients presenting with a stress microfracture during the course of the treatment had a higher gain in bone mass than those without stress fractures (at 1 yr+11 vs. +5%, p = 0.03 and at 18 months +18 vs. +6.9%, p < 0.02). In conclusion, there is a clear correlation between the efficacy and the occurrence of side effects of fluoride therapy in osteoporosis. In addition to the dose, the bioavailability of the fluoride salt may play a critical role in the magnitude of the response and should be taken into account when establishing the optimum therapeutic dose, as the therapeutic window may be narrow.