BONE LOSS AFTER CARDIAC TRANSPLANTATION - EFFECTS OF CALCIUM, CALCIDIOL AND MONOFLUOROPHOSPHATE

Of 203 patients who underwent cardiac transplantation and were given l ong-term treatment with cyclosporine and 0.3 mg/kg per day prednisone, 123 were studied prospectively for at least 6 months and 46 for up to 2 years to evaluate the effects on lumbar bone mineral density (BMD) and calcium metabolism of a combined therapy with calcium, calcidiol a nd disodium monofluorophosphate (MFP). The population was arbitrarily assigned to one of two groups. Group I consisted of patients who had a lumbar spine BMD Z score above -1.5 SD as compared with an age- and s ex-matched population and no vertebral fractures. They received daily 1 g elemental calcium and 25 mu g (1000 IU) calcidiol. Group II consis ted of patients who received daily the same doses of calcium and calci diol combined with 200 mg MFP, and was divided into two subgroups: (a) osteopenic subjects who had a lumbar spine BMD Z score below -1.5 SD without vertebral fractures and (b) osteoporotic subjects with vertebr al fractures. If serum creatinine was higher than 140 mu mol/l the dai ly dose of MFP was tapered to 100 mg. Fifty-four and 27 patients from group I and 38 and 19 patients from group II were followed respectivel y for 12 and 24 months. In both groups serum parathyroid hormone level s were significantly reduced from the twelfth month in parallel with a significant increase in serum 25-OHD levels. No decline in lumbar BMD occurred in non-osteopenic and nonosteoporotic patients (group I) who received the calcium and calcidiol supplement. In group II, where MFP was added, a significant and linear increase in lumbar BMD was observ ed. The average increase reached 12.5% after 12 months and 29.5% after 24 months (p<0.0001). The magnitude of the response was similar to th e response previously reported in patients suffering from vertebral fr actures due to postmenopausal osteoporosis and treated with the same d aily dose of MFP. Because osteoporosis and fractures are not rare in p atients after cardiac transplantation, these pilot results may be usef ul for further prevention and treatment trials of bone loss in this co ndition.