I. Garciadelgado et al., CALCITONIN, ETIDRONATE, AND CALCIDIOL TREATMENT IN BONE LOSS AFTER CARDIAC TRANSPLANTATION, Calcified tissue international, 60(2), 1997, pp. 155-159
Cardiac transplantation is associated with severe bone loss caused by
glucocorticoids, immunosuppressive treatment, and other factors. Treat
ment protocols for the prevention of bone loss is being studied. Forty
patients who underwent cardiac transplantation were randomly given ca
lcitonin (n = 13; 100 UI/d, nasal route), etidronate(n = 14; cyclical
treatment 400 mg p.o./d/2 weeks/3 months), or calcidiol (n = 13; 32,00
0 IU/weekly) therapy for at least 18 months. Serum parameters (Ca, P,
alkaline phosphatase, osteocalcin, intact PTH), urinary calcium, and v
ertebral mineral density (VMD; L2-L4, DXA Hologic QDR 1000) were measu
red immediately before treatment and after 6, 12, and 18 months of the
rapy after cardiac transplantation. Patients with cardiac transplantat
ion had a VMD significantly lower than age and sex-matched Spanish con
trols, Prevalence of osteoporosis (Z-score below -2 SD) was 30%. Osteo
calcin levels increased at 6, 12, and 18 months of treatment in the th
ree groups. After 18 months of treatment, VMD increased significantly
in the calcidiol 4.9%, vs. -1.19% and -0.19% in the calcitonin and eti
dronate groups, respectively. A lower incidence of fracture was found
in patients treated with calcidiol during the study. In summary, we ha
ve found in this open randomized study that calcidiol was the most eff
ective drug in the prevention and treatment of bone loss in patients a
fter cardiac transplantation.