Abstract
52 patients with OP identified AS were divided into 2 groups: group 1 - 24
patients receiving alphacalcidol 0.5-1 mcg "Mineralf", group 2 - 28 patients receiving 1000
mg of calcium. All indications were re-examined before and 6 months after treatment.
When patients were treated with alphacalcidol for 6 months, bone and spine pain decreased
by 27.2% (Ð <0.001) and muscle strength increased by 16.1% (R <0.05). In the control
group, no positive clinical results were observed. Patients responded well to alphacalcidol.
Side effects were almost non-existent. Only